Restoration of integrity to traumatized tissue.
Paired, segmented masses of MESENCHYME located on either side of the developing spinal cord (neural tube). Somites derive from PARAXIAL MESODERM and continue to increase in number during ORGANOGENESIS. Somites give rise to SKELETON (sclerotome); MUSCLES (myotome); and DERMIS (dermatome).
A vascular connective tissue formed on the surface of a healing wound, ulcer, or inflamed tissue. It consists of new capillaries and an infiltrate containing lymphoid cells, macrophages, and plasma cells.
Epidermal cells which synthesize keratin and undergo characteristic changes as they move upward from the basal layers of the epidermis to the cornified (horny) layer of the skin. Successive stages of differentiation of the keratinocytes forming the epidermal layers are basal cell, spinous or prickle cell, and the granular cell.
Devices intended to replace non-functioning organs. They may be temporary or permanent. Since they are intended always to function as the natural organs they are replacing, they should be differentiated from PROSTHESES AND IMPLANTS and specific types of prostheses which, though also replacements for body parts, are frequently cosmetic (EYE, ARTIFICIAL) as well as functional (ARTIFICIAL LIMBS).
An abnormal passage or communication leading from an internal organ to the surface of the body.
The outer covering of the body that protects it from the environment. It is composed of the DERMIS and the EPIDERMIS.
Human or animal tissue used as temporary wound coverings.
One or more layers of EPITHELIAL CELLS, supported by the basal lamina, which covers the inner or outer surfaces of the body.
Stratified squamous epithelium that covers the outer surface of the CORNEA. It is smooth and contains many free nerve endings.
The innermost membranous sac that surrounds and protects the developing embryo which is bathed in the AMNIOTIC FLUID. Amnion cells are secretory EPITHELIAL CELLS and contribute to the amniotic fluid.
Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like.
Diseases of the cornea.
The grafting of skin in humans or animals from one site to another to replace a lost portion of the body surface skin.
The middle germ layer of an embryo derived from three paired mesenchymal aggregates along the neural tube.
The transparent anterior portion of the fibrous coat of the eye consisting of five layers: stratified squamous CORNEAL EPITHELIUM; BOWMAN MEMBRANE; CORNEAL STROMA; DESCEMET MEMBRANE; and mesenchymal CORNEAL ENDOTHELIUM. It serves as the first refracting medium of the eye. It is structurally continuous with the SCLERA, avascular, receiving its nourishment by permeation through spaces between the lamellae, and is innervated by the ophthalmic division of the TRIGEMINAL NERVE via the ciliary nerves and those of the surrounding conjunctiva which together form plexuses. (Cline et al., Dictionary of Visual Science, 4th ed)
The movement of cells from one location to another. Distinguish from CYTOKINESIS which is the process of dividing the CYTOPLASM of a cell.
The processes occurring in early development that direct morphogenesis. They specify the body plan ensuring that cells will proceed to differentiate, grow, and diversify in size and shape at the correct relative positions. Included are axial patterning, segmentation, compartment specification, limb position, organ boundary patterning, blood vessel patterning, etc.
Cells that line the inner and outer surfaces of the body by forming cellular layers (EPITHELIUM) or masses. Epithelial cells lining the SKIN; the MOUTH; the NOSE; and the ANAL CANAL derive from ectoderm; those lining the RESPIRATORY SYSTEM and the DIGESTIVE SYSTEM derive from endoderm; others (CARDIOVASCULAR SYSTEM and LYMPHATIC SYSTEM) derive from mesoderm. Epithelial cells can be classified mainly by cell shape and function into squamous, glandular and transitional epithelial cells.
Any of the processes by which nuclear, cytoplasmic, or intercellular factors influence the differential control of gene action during the developmental stages of an organism.
Progressive restriction of the developmental potential and increasing specialization of function that leads to the formation of specialized cells, tissues, and organs.
Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others.
Rhenium. A metal, atomic number 75, atomic weight 186.2, symbol Re. (Dorland, 28th ed)
Mononuclear cells with pronounced phagocytic ability that are distributed extensively in lymphoid and other organs. It includes MACROPHAGES and their precursors; PHAGOCYTES; KUPFFER CELLS; HISTIOCYTES; DENDRITIC CELLS; LANGERHANS CELLS; and MICROGLIA. The term mononuclear phagocyte system has replaced the former reticuloendothelial system, which also included less active phagocytic cells such as fibroblasts and endothelial cells. (From Illustrated Dictionary of Immunology, 2d ed.)

Restoration of the rabbit corneal surface after total epithelial debridement and complete limbal excision. (1/25)

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Predictors of outcome in fungal keratitis. (2/25)

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A comparison of epithelial-to-mesenchymal transition and re-epithelialization. (3/25)

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A novel autologous cell-based therapy to promote diabetic wound healing. (4/25)

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Epithelial stem cells and implications for wound repair. (5/25)

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Age-related aspects of cutaneous wound healing: a mini-review. (6/25)

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Eccrine sweat glands are major contributors to reepithelialization of human wounds. (7/25)

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Repair of tracheal epithelium by basal cells after chlorine-induced injury. (8/25)

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Wound healing is a complex and dynamic process that occurs after tissue injury, aiming to restore the integrity and functionality of the damaged tissue. It involves a series of overlapping phases: hemostasis, inflammation, proliferation, and remodeling.

1. Hemostasis: This initial phase begins immediately after injury and involves the activation of the coagulation cascade to form a clot, which stabilizes the wound and prevents excessive blood loss.
2. Inflammation: Activated inflammatory cells, such as neutrophils and monocytes/macrophages, infiltrate the wound site to eliminate pathogens, remove debris, and release growth factors that promote healing. This phase typically lasts for 2-5 days post-injury.
3. Proliferation: In this phase, various cell types, including fibroblasts, endothelial cells, and keratinocytes, proliferate and migrate to the wound site to synthesize extracellular matrix (ECM) components, form new blood vessels (angiogenesis), and re-epithelialize the wounded area. This phase can last up to several weeks depending on the size and severity of the wound.
4. Remodeling: The final phase of wound healing involves the maturation and realignment of collagen fibers, leading to the restoration of tensile strength in the healed tissue. This process can continue for months to years after injury, although the tissue may never fully regain its original structure and function.

It is important to note that wound healing can be compromised by several factors, including age, nutrition, comorbidities (e.g., diabetes, vascular disease), and infection, which can result in delayed healing or non-healing chronic wounds.

Somites are transient, segmentally repeated embryonic structures that form along the anterior-posterior body axis during vertebrate development. They are derived from the paraxial mesoderm and give rise to various tissues, including the sclerotome (which forms the vertebrae and ribs), myotome (which forms the skeletal muscles of the back and limbs), and dermatome (which forms the dermis of the skin).

Each somite is a block-like structure that is arranged in a repeating pattern along the notochord, which is a flexible rod-like structure that provides mechanical support to the developing embryo. The formation of somites is a critical step in the development of the vertebrate body plan, as they help to establish the segmental organization of the musculoskeletal system and contribute to the formation of other important structures such as the dermis and the circulatory system.

The process of somitogenesis, or the formation of somites, is a highly regulated and coordinated event that involves the interaction of various signaling molecules and genetic pathways. Defects in somite formation can lead to a range of developmental abnormalities, including spinal deformities, muscle weakness, and skin defects.

Granulation tissue is the pinkish, bumpy material that forms on the surface of a healing wound. It's composed of tiny blood vessels (capillaries), white blood cells, and fibroblasts - cells that produce collagen, which is a protein that helps to strengthen and support the tissue.

Granulation tissue plays a crucial role in the wound healing process by filling in the wound space, contracting the wound, and providing a foundation for the growth of new skin cells (epithelialization). It's typically formed within 3-5 days after an injury and continues to develop until the wound is fully healed.

It's important to note that while granulation tissue is a normal part of the healing process, excessive or overgrowth of granulation tissue can lead to complications such as delayed healing, infection, or the formation of hypertrophic scars or keloids. In these cases, medical intervention may be necessary to manage the excess tissue and promote proper healing.

Keratinocytes are the predominant type of cells found in the epidermis, which is the outermost layer of the skin. These cells are responsible for producing keratin, a tough protein that provides structural support and protection to the skin. Keratinocytes undergo constant turnover, with new cells produced in the basal layer of the epidermis and older cells moving upward and eventually becoming flattened and filled with keratin as they reach the surface of the skin, where they are then shed. They also play a role in the immune response and can release cytokines and other signaling molecules to help protect the body from infection and injury.

Artificial organs are medical devices that are implanted in the human body to replace the function of a damaged, diseased, or failing organ. These devices can be made from a variety of materials, including metals, plastics, and synthetic biomaterials. They are designed to mimic the structure and function of natural organs as closely as possible, with the goal of improving the patient's quality of life and extending their lifespan.

Some examples of artificial organs include:

1. Artificial heart: A device that is implanted in the chest to replace the function of a failing heart. It can be used as a temporary or permanent solution for patients with end-stage heart failure.
2. Artificial pancreas: A device that is used to treat type 1 diabetes by regulating blood sugar levels. It consists of an insulin pump and a continuous glucose monitor, which work together to deliver insulin automatically based on the patient's needs.
3. Artificial kidney: A device that filters waste products from the blood, similar to a natural kidney. It can be used as a temporary or permanent solution for patients with end-stage renal disease.
4. Artificial lung: A device that helps patients with respiratory failure breathe by exchanging oxygen and carbon dioxide in the blood.
5. Artificial bladder: A device that is implanted in the body to help patients with bladder dysfunction urinate.
6. Artificial eyes: Prosthetic devices that are used to replace a missing or damaged eye, providing cosmetic and sometimes functional benefits.

It's important to note that while artificial organs can significantly improve the quality of life for many patients, they are not without risks. Complications such as infection, rejection, and device failure can occur, and ongoing medical care is necessary to monitor and manage these risks.

A cutaneous fistula is a type of fistula that occurs when a tract or tunnel forms between the skin (cutaneous) and another organ or structure, such as the gastrointestinal tract, vagina, or urinary system. Cutaneous fistulas can result from various medical conditions, including infections, inflammatory diseases, surgical complications, trauma, or malignancies.

Cutaneous fistulas may present with symptoms such as drainage of fluid or pus from the skin, pain, redness, swelling, or irritation around the affected area. The treatment for cutaneous fistulas depends on their underlying cause and can range from conservative management with antibiotics and wound care to surgical intervention.

It is essential to seek medical attention if you suspect a cutaneous fistula, as untreated fistulas can lead to complications such as infection, sepsis, or tissue damage. A healthcare professional can provide an accurate diagnosis and develop an appropriate treatment plan based on the individual's needs.

In medical terms, the skin is the largest organ of the human body. It consists of two main layers: the epidermis (outer layer) and dermis (inner layer), as well as accessory structures like hair follicles, sweat glands, and oil glands. The skin plays a crucial role in protecting us from external factors such as bacteria, viruses, and environmental hazards, while also regulating body temperature and enabling the sense of touch.

"Biological dressings" refer to materials used in wound healing that are derived from biological sources, such as living cells, tissues, or extracellular matrix components. These dressings can be used to promote the regeneration and repair of damaged or injured tissues by providing a supportive environment for cell growth, differentiation, and tissue formation.

Biological dressings may be derived from various sources, including:

1. Autografts: Tissue harvested from the same individual who will receive the graft.
2. Allografts: Tissue harvested from a donor of the same species.
3. Xenografts: Tissue harvested from a donor of a different species.
4. Decellularized tissue matrices: Tissues that have had their cellular components removed, leaving behind an intact extracellular matrix scaffold.
5. Engineered tissues: Tissues created in the lab through the cultivation and assembly of cells on biocompatible scaffolds or hydrogels.

Examples of biological dressings include skin substitutes, amniotic membranes, and platelet-rich plasma (PRP) preparations. These dressings can help to reduce inflammation, prevent infection, and enhance the healing process in various types of wounds, including chronic wounds, burns, and surgical incisions.

It is important to note that while biological dressings offer several advantages over traditional wound dressings, they may also carry risks such as immune rejection or disease transmission, depending on their source and preparation. Therefore, careful consideration should be given to the selection of appropriate biological dressing materials for each individual patient and application.

Epithelium is the tissue that covers the outer surface of the body, lines the internal cavities and organs, and forms various glands. It is composed of one or more layers of tightly packed cells that have a uniform shape and size, and rest on a basement membrane. Epithelial tissues are avascular, meaning they do not contain blood vessels, and are supplied with nutrients by diffusion from the underlying connective tissue.

Epithelial cells perform a variety of functions, including protection, secretion, absorption, excretion, and sensation. They can be classified based on their shape and the number of cell layers they contain. The main types of epithelium are:

1. Squamous epithelium: composed of flat, scalelike cells that fit together like tiles on a roof. It forms the lining of blood vessels, air sacs in the lungs, and the outermost layer of the skin.
2. Cuboidal epithelium: composed of cube-shaped cells with equal height and width. It is found in glands, tubules, and ducts.
3. Columnar epithelium: composed of tall, rectangular cells that are taller than they are wide. It lines the respiratory, digestive, and reproductive tracts.
4. Pseudostratified epithelium: appears stratified or layered but is actually made up of a single layer of cells that vary in height. The nuclei of these cells appear at different levels, giving the tissue a stratified appearance. It lines the respiratory and reproductive tracts.
5. Transitional epithelium: composed of several layers of cells that can stretch and change shape to accommodate changes in volume. It is found in the urinary bladder and ureters.

Epithelial tissue provides a barrier between the internal and external environments, protecting the body from physical, chemical, and biological damage. It also plays a crucial role in maintaining homeostasis by regulating the exchange of substances between the body and its environment.

The corneal epithelium is the outermost layer of the cornea, which is the clear, dome-shaped surface at the front of the eye. It is a stratified squamous epithelium, consisting of several layers of flat, scale-like cells that are tightly packed together. The corneal epithelium serves as a barrier to protect the eye from microorganisms, dust, and other foreign particles. It also provides a smooth surface for the refraction of light, contributes to the maintenance of corneal transparency, and plays a role in the eye's sensitivity to touch and pain. The corneal epithelium is constantly being renewed through the process of cell division and shedding, with new cells produced by stem cells located at the limbus, the border between the cornea and the conjunctiva.

The amnion is the innermost fetal membrane in mammals, forming a sac that contains and protects the developing embryo and later the fetus within the uterus. It is one of the extraembryonic membranes that are derived from the outer cell mass of the blastocyst during early embryonic development. The amnion is filled with fluid (amniotic fluid) that allows for the freedom of movement and protection of the developing fetus.

The primary function of the amnion is to provide a protective environment for the growing fetus, allowing for expansion and preventing physical damage from outside forces. Additionally, the amniotic fluid serves as a medium for the exchange of waste products and nutrients between the fetal membranes and the placenta. The amnion also contributes to the formation of the umbilical cord and plays a role in the initiation of labor during childbirth.

Burns are injuries to tissues caused by heat, electricity, chemicals, friction, or radiation. They are classified based on their severity:

1. First-degree burns (superficial burns) affect only the outer layer of skin (epidermis), causing redness, pain, and swelling.
2. Second-degree burns (partial-thickness burns) damage both the epidermis and the underlying layer of skin (dermis). They result in redness, pain, swelling, and blistering.
3. Third-degree burns (full-thickness burns) destroy the entire depth of the skin and can also damage underlying muscles, tendons, and bones. These burns appear white or blackened and charred, and they may be painless due to destroyed nerve endings.

Immediate medical attention is required for second-degree and third-degree burns, as well as for large area first-degree burns, to prevent infection, manage pain, and ensure proper healing. Treatment options include wound care, antibiotics, pain management, and possibly skin grafting or surgery in severe cases.

Corneal diseases are a group of disorders that affect the cornea, which is the clear, dome-shaped surface at the front of the eye. The cornea plays an important role in focusing vision, and any damage or disease can cause significant visual impairment or loss. Some common types of corneal diseases include:

1. Keratoconus: A progressive disorder in which the cornea thins and bulges outward into a cone shape, causing distorted vision.
2. Fuchs' dystrophy: A genetic disorder that affects the inner layer of the cornea called the endothelium, leading to swelling, cloudiness, and decreased vision.
3. Dry eye syndrome: A condition in which the eyes do not produce enough tears or the tears evaporate too quickly, causing discomfort, redness, and blurred vision.
4. Corneal ulcers: Open sores on the cornea that can be caused by infection, trauma, or other factors.
5. Herpes simplex keratitis: A viral infection of the cornea that can cause recurrent episodes of inflammation, scarring, and vision loss.
6. Corneal dystrophies: Inherited disorders that affect the structure and clarity of the cornea, leading to visual impairment or blindness.
7. Bullous keratopathy: A condition in which the endothelium fails to pump fluid out of the cornea, causing it to swell and form blisters.
8. Corneal trauma: Injury to the cornea caused by foreign objects, chemicals, or other factors that can lead to scarring, infection, and vision loss.

Treatment for corneal diseases varies depending on the specific condition and severity of the disease. Options may include eyedrops, medications, laser surgery, corneal transplantation, or other treatments.

Skin transplantation, also known as skin grafting, is a surgical procedure that involves the removal of healthy skin from one part of the body (donor site) and its transfer to another site (recipient site) that has been damaged or lost due to various reasons such as burns, injuries, infections, or diseases. The transplanted skin can help in healing wounds, restoring functionality, and improving the cosmetic appearance of the affected area. There are different types of skin grafts, including split-thickness grafts, full-thickness grafts, and composite grafts, which vary in the depth and size of the skin removed and transplanted. The success of skin transplantation depends on various factors, including the size and location of the wound, the patient's overall health, and the availability of suitable donor sites.

In medical and embryological terms, the mesoderm is one of the three primary germ layers in the very early stages of embryonic development. It forms between the ectoderm and endoderm during gastrulation, and it gives rise to a wide variety of cell types, tissues, and organs in the developing embryo.

The mesoderm contributes to the formation of structures such as:

1. The connective tissues (including tendons, ligaments, and most of the bones)
2. Muscular system (skeletal, smooth, and cardiac muscles)
3. Circulatory system (heart, blood vessels, and blood cells)
4. Excretory system (kidneys and associated structures)
5. Reproductive system (gonads, including ovaries and testes)
6. Dermis of the skin
7. Parts of the eye and inner ear
8. Several organs in the urogenital system

Dysfunctions or abnormalities in mesoderm development can lead to various congenital disorders and birth defects, highlighting its importance during embryogenesis.

The cornea is the clear, dome-shaped surface at the front of the eye. It plays a crucial role in focusing vision. The cornea protects the eye from harmful particles and microorganisms, and it also serves as a barrier against UV light. Its transparency allows light to pass through and get focused onto the retina. The cornea does not contain blood vessels, so it relies on tears and the fluid inside the eye (aqueous humor) for nutrition and oxygen. Any damage or disease that affects its clarity and shape can significantly impact vision and potentially lead to blindness if left untreated.

Cell movement, also known as cell motility, refers to the ability of cells to move independently and change their location within tissue or inside the body. This process is essential for various biological functions, including embryonic development, wound healing, immune responses, and cancer metastasis.

There are several types of cell movement, including:

1. **Crawling or mesenchymal migration:** Cells move by extending and retracting protrusions called pseudopodia or filopodia, which contain actin filaments. This type of movement is common in fibroblasts, immune cells, and cancer cells during tissue invasion and metastasis.
2. **Amoeboid migration:** Cells move by changing their shape and squeezing through tight spaces without forming protrusions. This type of movement is often observed in white blood cells (leukocytes) as they migrate through the body to fight infections.
3. **Pseudopodial extension:** Cells extend pseudopodia, which are temporary cytoplasmic projections containing actin filaments. These protrusions help the cell explore its environment and move forward.
4. **Bacterial flagellar motion:** Bacteria use a whip-like structure called a flagellum to propel themselves through their environment. The rotation of the flagellum is driven by a molecular motor in the bacterial cell membrane.
5. **Ciliary and ependymal movement:** Ciliated cells, such as those lining the respiratory tract and fallopian tubes, have hair-like structures called cilia that beat in coordinated waves to move fluids or mucus across the cell surface.

Cell movement is regulated by a complex interplay of signaling pathways, cytoskeletal rearrangements, and adhesion molecules, which enable cells to respond to environmental cues and navigate through tissues.

"Body patterning" is a general term that refers to the process of forming and organizing various tissues and structures into specific patterns during embryonic development. This complex process involves a variety of molecular mechanisms, including gene expression, cell signaling, and cell-cell interactions. It results in the creation of distinct body regions, such as the head, trunk, and limbs, as well as the organization of internal organs and systems.

In medical terminology, "body patterning" may refer to specific developmental processes or abnormalities related to embryonic development. For example, in genetic disorders such as Poland syndrome or Holt-Oram syndrome, mutations in certain genes can lead to abnormal body patterning, resulting in the absence or underdevelopment of certain muscles, bones, or other structures.

It's important to note that "body patterning" is not a formal medical term with a specific definition, but rather a general concept used in developmental biology and genetics.

Epithelial cells are types of cells that cover the outer surfaces of the body, line the inner surfaces of organs and glands, and form the lining of blood vessels and body cavities. They provide a protective barrier against the external environment, regulate the movement of materials between the internal and external environments, and are involved in the sense of touch, temperature, and pain. Epithelial cells can be squamous (flat and thin), cuboidal (square-shaped and of equal height), or columnar (tall and narrow) in shape and are classified based on their location and function.

Developmental gene expression regulation refers to the processes that control the activation or repression of specific genes during embryonic and fetal development. These regulatory mechanisms ensure that genes are expressed at the right time, in the right cells, and at appropriate levels to guide proper growth, differentiation, and morphogenesis of an organism.

Developmental gene expression regulation is a complex and dynamic process involving various molecular players, such as transcription factors, chromatin modifiers, non-coding RNAs, and signaling molecules. These regulators can interact with cis-regulatory elements, like enhancers and promoters, to fine-tune the spatiotemporal patterns of gene expression during development.

Dysregulation of developmental gene expression can lead to various congenital disorders and developmental abnormalities. Therefore, understanding the principles and mechanisms governing developmental gene expression regulation is crucial for uncovering the etiology of developmental diseases and devising potential therapeutic strategies.

Cell differentiation is the process by which a less specialized cell, or stem cell, becomes a more specialized cell type with specific functions and structures. This process involves changes in gene expression, which are regulated by various intracellular signaling pathways and transcription factors. Differentiation results in the development of distinct cell types that make up tissues and organs in multicellular organisms. It is a crucial aspect of embryonic development, tissue repair, and maintenance of homeostasis in the body.

"Cells, cultured" is a medical term that refers to cells that have been removed from an organism and grown in controlled laboratory conditions outside of the body. This process is called cell culture and it allows scientists to study cells in a more controlled and accessible environment than they would have inside the body. Cultured cells can be derived from a variety of sources, including tissues, organs, or fluids from humans, animals, or cell lines that have been previously established in the laboratory.

Cell culture involves several steps, including isolation of the cells from the tissue, purification and characterization of the cells, and maintenance of the cells in appropriate growth conditions. The cells are typically grown in specialized media that contain nutrients, growth factors, and other components necessary for their survival and proliferation. Cultured cells can be used for a variety of purposes, including basic research, drug development and testing, and production of biological products such as vaccines and gene therapies.

It is important to note that cultured cells may behave differently than they do in the body, and results obtained from cell culture studies may not always translate directly to human physiology or disease. Therefore, it is essential to validate findings from cell culture experiments using additional models and ultimately in clinical trials involving human subjects.

I'm sorry for any confusion, but "Rhenium" is not a medical term. It is a chemical element with the symbol "Re" and atomic number 75. Rhenium is a heavy, silvery-white, metallic element that is highly resistant to corrosion and is used in high-temperature alloys and electronics.

It does not have any direct medical relevance or application as a drug, treatment, or diagnostic tool in human medicine. However, like many other elements, rhenium compounds are being studied for their potential medicinal uses, such as in cancer therapy. But it's important to note that these are still in the research phase and have not yet been approved for use in humans.

The Mononuclear Phagocyte System (MPS) is a network of specialized immune cells distributed throughout the body, primarily consisting of monocytes, macrophages, and dendritic cells. These cells share a common bone marrow-derived precursor and play crucial roles in innate and adaptive immunity. They are involved in various functions such as:

1. Phagocytosis: engulfing and destroying foreign particles, microbes, and cellular debris.
2. Antigen presentation: processing and presenting antigens to T-cells to initiate an adaptive immune response.
3. Cytokine production: releasing pro- and anti-inflammatory cytokines to regulate immune responses and maintain tissue homeostasis.
4. Immune regulation: modulating the activity of other immune cells, including T-cells, B-cells, and natural killer (NK) cells.

The MPS is essential for maintaining tissue integrity, fighting infections, and orchestrating immune responses. Its components are found in various tissues, including the liver (Kupffer cells), spleen, lymph nodes, bone marrow, and connective tissues.

"Re-Epithelialization" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical ... This graph shows the total number of publications written about "Re-Epithelialization" by people in this website by year, and ... Below are the most recent publications written about "Re-Epithelialization" by people in Profiles. ... Below are MeSH descriptors whose meaning is more general than "Re-Epithelialization". ...
Epithelialization. Epithelialization is the formation of epithelium over a denuded surface. It involves the migration of cells ... When epithelialization is complete, the epidermal cell assumes its original form, and new desmosomal linkages to other ... Epithelialization, fibroplasia, and angiogenesis occur during the proliferative phase. Meanwhile, granulation tissue forms and ... Given the fact that angiogenesis and epithelialization take longer in secondary intention healing, these wounds are more prone ...
... hence the need to develop a corneal inlay to aid in corneal re-epithelialization. Transparent epoxy-functional polymethacrylate ... Amine functional hydrogels as selective substrates for corneal epithelialization. Acta Biomaterialia. 10(7): 3029-3037. ...
Cheng et al conclude that the accelerated wound healing observed was due to accelerated epithelialization rather than ... Fibronectin, Wound Contraction, and Epithelialization. Arch Dermatol. 1988;124(8):1183-1184. doi:10.1001/archderm. ...
LINK Congress 2019, Epithelialization Language. EN Publication Year. 2019 Author(s). Marjana Tomic-Canic Approx. reading time. ... Keratinocytes under the spotlight: Epithelialization process is essential for wound healing. Type. Congress Abstract Topics. ... Epithelialization is also impaired in these patients. Details of biological functions of keratinocytes during healthy and ... A comprehensive understanding of the epithelialization process will provide new tools for clinical approaches to facilitate ...
... Abate M.; ... providing the first evidence of its capability to accelerate the healing processes enhancing re-epithelialization and to ... providing the first evidence of its capability to accelerate the healing processes enhancing re-epithelialization and to ...
inflammation, •epithelialization, •angiogenesis •and matrix deposition. Fig. 1. Wound healing is a complex process encompassing ...
Epithelialization.. *Ulcer pain.. *Current stage.. *Followup status (improving, no change, worsening) per nurse observation. ...
Re-epithelialization occurs within the first 48 hours post-amputation, in the middle of the repair phase. Interestingly, in ... "Epithelialization in Wound Healing: A Comprehensive Review". Advances in Wound Care. 3 (7): 445-464. doi:10.1089/wound. ... contrast to most mammals, starfish accomplish re-epithelialization without any immediate proliferation of epidermal progenitor ...
Epithelialization in Wound Healing: A Comprehensive Review. Adv Wound Care (New Rochelle) 3, 445-464, 10.1089/wound.2013.0473 ( ... Furthermore, keratinocyte migration and proliferation are critical for re-epithelialization of skin wounds7. Fibroblasts ... modulate keratinocyte migration and proliferation which are considered key events in wound healing during re-epithelialization ...
Re-Epithelialization* * Receptors, Notch / metabolism * Signal Transduction * Stem Cell Transplantation * Stem Cells / cytology ...
A colloidal oat spray displays a healing effect in skin, inducing re-epithelialization.Jan 01, 2005. ...
Figure 8. Subpleural fibrosis and epithelialization.. Figure 9. Mature interstitial fibrosis. Pathogenesis. Interstitial ...
More recently, calcium alginate aerogels impregnated with mesoglycan were developed to favor the re-epithelialization and ... epithelialization). During this stage, dark, shiny red granulation tissue fills the wound bed with connective tissue and new ... the deposition of ECM and epithelialization [1,3]. The epithelial cell proliferation starts with chemotactic stimulation with ...
Exuberant granulation tissues can significantly delay epithelialization. Steroid creams, steroid-containing drops, and regular ... Open cavities heal slowly, and 12-24 weeks are often required for full epithelialization. ...
Ear Packing that Enhances Epithelialization. EpiFilm® and EpiDisc® Otologic Laminae are unique bioresorbable, implantable ear ... EpiFilm and EpiDisc Otologic Laminae physically enhance the epithelialization process. In approximately 6-8 weeks, the ...
Primarily, time to ,95% wound closure or re-epithelialization. Finally, number of debridement procedures and percentage ... because bromelain can improve the debridement mechanism and provide quicker healing and more effective re-epithelialization [92 ...
Amine functional hydrogels as selective substrates for corneal epithelialization. E. Hassan, P. Deshpande, F. Claeyssens, S. ...
First, the re-epithelialization of the damaged skin takes place, due to the proliferation of the keratinocytes located at the ... The MSC-derived EV increased the skin re-epithelialization in full-thickness cutaneous wounds in animal models (Robson et al., ... The keratinocytes intervene in the re-epithelialization of skin. That is considered as one of the major processes in wound ... Therefore, they are essential for skin re-epithelialization. On the other hand, the dermis is located below the epidermis, ...
2009). 5alpha-dihydrotestosterone (DHT) retards wound closure by inhibiting re-epithelialization. DOI:. https://doi.org/10.1002 ...
... wounds treated with T-HDCG had decreased total healing at day 8 and decreased epithelialization and decreased total healing at ... topical application of T-HDCG to wounds had a negative effect on second intention healing by delaying the epithelialization ... Wounds were monitored for contraction, epithelialization, and complete healing at 4, 8, and 14 days after wound creation. The ... Analysis of percentages of epithelialization, wound contraction, and total healing-On day 4, there was no epithelialization of ...
However, KRT5+ cells become actively involved in re-epithelialization after mechanical damage. Our preliminary results suggest ...
Complete epithelialization is reached in about 1 month, while complete connective tissue repair takes 7-8 weeks. After this, no ... Epithelialization from the peripheral gingival margins starts within 24 hours and becomes complete after 1-5 weeks in relation ... Subsequently, the superficial layer of the graft becomes veil-like, thin and gray following new epithelialization from adjacent ... degree of tissue epithelialization (partial/complete); presence/absence of bleeding; presence/absence of pain on palpation68. ...
Delayed corneal wound healing and re-epithelialization may result.20. Aspirin or other anticoagulants may be taken without ...
Epithelialisation phase: The duration of the epithelialisation phase depends on the size of the wound. Surface cells multiply ...
Epithelialisation. Maturation / Contraction. As there are many factors to consider when trying to manage a complex, slow-to- ...
This lesion consisted of interstitial fibrosis, alveolar epithelialization, and mononuclear cell infiltration. No other ...
Interstitial pneumonia showing fibrotic thickening of alveolar walls and epithelialization of pneumocytes (hematoxylin and ...
Healing was defined as complete epithelialisation, regardless of residual pain. Maintenance of cardinal ulcer healing required ...
Surface epithelialization of the type I Boston keratoprosthesis front plate: immunohistochemical and high-definition optical ...

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