Cytoskeleton
Actin Cytoskeleton
Actins
Microfilament Proteins
Cytochalasin D
Cytoskeletal Proteins
Microtubules
Bicyclo Compounds, Heterocyclic
rho GTP-Binding Proteins
Cell Polarity
Phalloidine
Microscopy, Fluorescence
cdc42 GTP-Binding Protein
Tubulin
Cell Movement
Stress Fibers
Pseudopodia
Signal Transduction
rhoA GTP-Binding Protein
Cells, Cultured
Depsipeptides
Cell Membrane
Intermediate Filaments
Protein Binding
Vinculin
Contractile Proteins
Colchicine
Actin Depolymerizing Factors
Membrane Proteins
rac1 GTP-Binding Protein
Focal Adhesions
Phosphorylation
Actinin
Microscopy, Confocal
Filamins
Molecular Sequence Data
Spectrin
Cytochalasins
Amino Acid Sequence
rac GTP-Binding Proteins
rho-Associated Kinases
Models, Biological
Fluorescent Antibody Technique
Protein Transport
Cortactin
Talin
Octoxynol
Protein Structure, Tertiary
Lim Kinases
Nocodazole
Carrier Proteins
Cadherins
Recombinant Fusion Proteins
Cell Surface Extensions
Mutation
Microscopy, Electron
Wiskott-Aldrich Syndrome Protein
Intercellular Junctions
Vimentin
Paxillin
Mechanotransduction, Cellular
Myosin Type II
Green Fluorescent Proteins
alpha Catenin
Adherens Junctions
Myosins
Endocytosis
Cytoplasm
Gelsolin
Microtubule-Associated Proteins
Integrins
Epithelial Cells
Transfection
Stress, Mechanical
Actomyosin
Adaptor Proteins, Signal Transducing
Guanine Nucleotide Exchange Factors
Fibroblasts
Profilins
Cell Adhesion Molecules
Ankyrins
Microscopy, Video
Tubulin Modulators
Destrin
Two-Hybrid System Techniques
Microtubule-Organizing Center
Dictyostelium
Polymerization
COS Cells
Blotting, Western
Extracellular Matrix
Actin-Related Protein 2-3 Complex
GTP-Binding Proteins
rhoB GTP-Binding Protein
3T3 Cells
Drosophila Proteins
Protein-Serine-Threonine Kinases
p21-Activated Kinases
Protein-Tyrosine Kinases
Sulfanilamides
Intracellular Signaling Peptides and Proteins
Detergents
Focal Adhesion Protein-Tyrosine Kinases
Enzyme Activation
Membrane Microdomains
Sequence Homology, Amino Acid
Actin-Related Protein 2
Phosphatidylinositol 4,5-Diphosphate
Calcium
Focal Adhesion Kinase 1
Luminescent Proteins
Morphogenesis
Cofilin 1
Keratins
Protein Isoforms
HeLa Cells
Immunoprecipitation
Saccharomyces cerevisiae
Blood Platelets
Biological Transport
Tyrosine
Wiskott-Aldrich Syndrome Protein Family
Neurofilament Proteins
Wiskott-Aldrich Syndrome Protein, Neuronal
Actin-Related Protein 3
Growth Cones
Binding Sites
Phenotype
Immunoblotting
Plectin
Saccharomyces cerevisiae Proteins
Proteins
NIH 3T3 Cells
src Homology Domains
Calmodulin-Binding Proteins
cdc42 GTP-Binding Protein, Saccharomyces cerevisiae
Immunohistochemistry
Actin Capping Proteins
Intermediate Filament Proteins
RNA Interference
Subcellular Fractions
Fibronectins
Cell Nucleus
Fluorescence Recovery After Photobleaching
Neurons
Enzyme Inhibitors
Cell Compartmentation
Neurofibromin 2
Drosophila
Embryo, Nonmammalian
Microscopy, Electron, Scanning
RNA, Small Interfering
Cytoplasmic Streaming
Podocytes
Polymers
Tight Junctions
src-Family Kinases
Cercopithecus aethiops
Antigens, CD29
Nonmuscle Myosin Type IIA
Precipitin Tests
Exocytosis
Erythrocyte Membrane
Electrophoresis, Polyacrylamide Gel
Cricetinae
Amides
Protein Kinase C
Base Sequence
Cell Division
Microscopy, Immunoelectron
LIM Domain Proteins
Biopolymers
Wiskott-Aldrich Syndrome
Zyxin
Myosin Type I
Proto-Oncogene Proteins pp60(c-src)
Fluorescent Antibody Technique, Indirect
Cell Differentiation
ras GTPase-Activating Proteins
Organelles
Desmoplakins
The cytoskeletal network controls c-Jun expression and glucocorticoid receptor transcriptional activity in an antagonistic and cell-type-specific manner. (1/10346)
The physical and functional link between adhesion molecules and the cytoskeletal network suggests that the cytoskeleton might mediate the transduction of cell-to-cell contact signals, which often regulate growth and differentiation in an antagonistic manner. Depolymerization of the cytoskeleton in confluent cell cultures is reportedly sufficient to initiate DNA synthesis. Here we show that depolymerization of the cytoskeleton is also sufficient to repress differentiation-specific gene expression. Glutamine synthetase is a glia-specific differentiation marker gene whose expression in the retinal tissue is regulated by glucocorticoids and is ultimately dependent on glia-neuron cell contacts. Depolymerization of the actin or microtubule network in cells of the intact retina mimics the effects of cell separation, repressing glutamine synthetase induction by a mechanism that involves induction of c-Jun and inhibition of glucocorticoid receptor transcriptional activity. Depolymerization of the cytoskeleton activates JNK and p38 mitogen-activated protein kinase and induces c-Jun expression by a signaling pathway that depends on tyrosine kinase activity. Induction of c-Jun expression is restricted to Muller glial cells, the only cells in the tissue that express glutamine synthetase and maintain the ability to proliferate upon cell separation. Our results suggest that the cytoskeletal network might play a part in the transduction of cell contact signals to the nucleus. (+info)Vibrio parahaemolyticus thermostable direct hemolysin modulates cytoskeletal organization and calcium homeostasis in intestinal cultured cells. (2/10346)
Vibrio parahaemolyticus is a marine bacterium known to be the leading cause of seafood gastroenteritis worldwide. A 46-kDa homodimer protein secreted by this microorganism, the thermostable direct hemolysin (TDH), is considered a major virulence factor involved in bacterial pathogenesis since a high percentage of strains of clinical origin are positive for TDH production. TDH is a pore-forming toxin, and its most extensively studied effect is the ability to cause hemolysis of erythrocytes from different mammalian species. Moreover, TDH induces in a variety of cells cytotoxic effects consisting mainly of cell degeneration which often leads to loss of viability. In this work, we examined the cellular changes induced by TDH in monolayers of IEC-6 cells (derived from the rat crypt small intestine), which represent a useful cell model for studying toxins from enteric bacteria. In experimental conditions allowing cell survival, TDH induces a rapid transient increase in intracellular calcium as well as a significant though reversible decreased rate of progression through the cell cycle. The morphological changes seem to be dependent on the organization of the microtubular network, which appears to be the preferential cytoskeletal element involved in the cellular response to the toxin. (+info)Interleukin-12 is synthesized by mesangial cells and stimulates platelet-activating factor synthesis, cytoskeletal reorganization, and cell shape change. (3/10346)
Preliminary studies indicate the involvement of interleukin (IL)-12 in experimental renal pathology. In the present study, we evaluated whether cultured glomerular mesangial cells are able to produce IL-12 and whether IL-12 may regulate some of their functions, including the cytoskeletal reorganization, the change in cell shape, and the production of platelet-activating factor (PAF). The results obtained indicate that pro-inflammatory stimuli, such as tumor necrosis factor-alpha and bacterial polysaccharides, induce the expression of IL-12 mRNA and the synthesis of the protein by cultured mesangial cells. Moreover, cultured mesangial cells were shown to bind IL-12 and to express the human low-affinity IL-12 beta1-chain receptor. When challenged with IL-12, mesangial cells produced PAF in a dose- and time-dependent manner and superoxide anions. No production of tumor necrosis factor-alpha and IL-8 was observed. Moreover, we demonstrate that IL-12 induced a delayed and sustained shape change of mesangial cells that reached its maximum between 90 and 120 minutes of incubation. The changes in cell shape occurred concomitantly with cytoskeletal rearrangements and may be consistent with cell contraction. As IL-12-dependent shape change of mesangial cells was concomitant with the synthesis of PAF, which is known to promote mesangial cell contraction, we investigated the role of PAF using two chemically different PAF receptor antagonists. Both antagonists inhibited almost completely the cell shape change induced by IL-12, whereas they were ineffective on angiotensin-II-induced cell shape change. In conclusion, our results suggest that mesangial cells can either produce IL-12 or be stimulated by this cytokine to synthesize PAF and to undergo shape changes compatible with cell contraction. (+info)Nitric oxide modulates endothelin 1-induced Ca2+ mobilization and cytoskeletal F-actin filaments in human cerebromicrovascular endothelial cells. (4/10346)
A functional interrelation between nitric oxide (NO), the endothelial-derived vasodilating factor, and endothelin 1 (ET-1), the potent vasoconstrictive peptide, was investigated in microvascular endothelium of human brain. Nor-1 dose-dependently decreased the ET-1-stimulated mobilization of Ca2+. This response was mimicked with cGMP and abrogated by inhibitors of guanylyl cyclase or cGMP-dependent protein kinase G. These findings indicate that NO and ET-1 interactions involved in modulation of intracellular Ca2+ are mediated by cGMP/protein kinase G. In addition, Nor-1-mediated effects were associated with rearrangements of cytoskeleton F-actin filaments. The results suggest mechanisms by which NO-ET-1 interactions may contribute to regulation of microvascular function. (+info)EB1, a protein which interacts with the APC tumour suppressor, is associated with the microtubule cytoskeleton throughout the cell cycle. (5/10346)
The characteristics of the adenomatous polyposis coli (APC) associated protein EB1 were examined in mammalian cells. By immunocytochemistry EB1 was shown to be closely associated with the microtubule cytoskeleton throughout the cell cycle. In interphase cells EB1 was associated with microtubules along their full length but was often particularly concentrated at their tips. During early mitosis, EB1 was localized to separating centrosomes and associated microtubules, while at metaphase it was associated with the spindle poles and associated microtubules. During cytokinesis EB1 was strongly associated with the midbody microtubules. Treatment with nocodazole caused a diffuse redistribution of EB1 immunoreactivity, whereas treatment with cytochalasin D had no effect. Interestingly, treatment with taxol abolished the EB1 association with microtubules. In nocodazole washout experiments EB1 rapidly became associated with the centrosome and repolymerizing microtubules. In taxol wash-out experiments EB1 rapidly re-associated with the microtubule cytoskeleton, resembling untreated control cells within 10 min. Immunostaining of SW480 cells, which contain truncated APC incapable of interaction with EB1, showed that the association of EB1 with microtubules throughout the cell cycle was not dependent upon an interaction with APC. These results suggest a role for EB1 in the control of microtubule dynamics in mammalian cells. (+info)Homotypic and heterotypic interaction of the neurofibromatosis 2 tumor suppressor protein merlin and the ERM protein ezrin. (6/10346)
Ezrin, radixin and moesin (ERM) are homologous proteins, which are linkers between plasma membrane components and the actin-containing cytoskeleton. The ERM protein family members associate with each other in a homotypic and heterotypic manner. The neurofibromatosis 2 (NF2) tumor suppressor protein merlin (schwannomin) is structurally related to ERM members. Merlin is involved in tumorigenesis of NF2-associated and sporadic schwannomas and meningiomas, but the tumor suppressor mechanism is poorly understood. We have studied the ability of merlin to self-associate and bind ezrin. Ezrin was coimmunoprecipitated with merlin from lysates of human U251 glioma cells and from COS-1 cells transfected with cDNA encoding for merlin isoform I. The interaction was further studied and the association domains were mapped with the yeast two-hybrid system and with blot overlay and affinity precipitation experiments. The heterotypic binding of merlin and ezrin and the homotypic association of merlin involves interaction between the amino- and carboxy-termini. The amino-terminal association domain of merlin involves residues 1-339 and has similar features with the amino-terminal association domain of ezrin. The carboxy-terminal association domain cannot be mapped as precisely as in ezrin, but it requires residues 585-595 and a more amino-terminal segment. Unlike ezrin, merlin does not require activation for self-association but native merlin molecules can interact with each other. Heterodimerization between merlin and ezrin, however, occurs only following conformational alterations in both proteins. These results biochemically connect merlin to the cortical cytoskeleton and indicate differential regulation of merlin from ERM proteins. (+info)Regulation of p190 Rho-GAP by v-Src is linked to cytoskeletal disruption during transformation. (7/10346)
The v-Src oncoprotein perturbs the dynamic regulation of the cellular cytoskeletal and adhesion network by a mechanism that is poorly understood. Here, we have examined in detail the effects of a temperature-dependent v-Src protein on the regulation of p190 RhoGAP, a GTPase activating protein (GAP) that has been implicated in disruption of the organised actin cytoskeleton, and addressed the dependence of v-Src-induced stress fibre loss on inhibition of Rho activity. We found that activation of v-Src induced association of tyrosine phosphorylated p190 with p120(RasGAP) and stimulation of p120(RasGAP)-associated RhoGAP activity, although p120(RasGAP) itself was not a target for phosphorylation by v-Src in chicken embryo cells. These events required the catalytic activity of v-Src and were linked to loss of actin stress fibres during morphological transformation and not mitogenic signalling. Furthermore, these effects were rapidly reversible since switching off v-Src led to dissociation of the p190/p120(RasGAP) complex, inactivation of p120(RasGAP)-associated RhoGAP activity and re-induction of actin stress fibres. In addition, transient transfection of Val14-RhoA, a constitutively active Rho protein that is insensitive to RhoGAPs, suppressed v-Src-induced stress fibre loss and cell transformation. Thus, we show here for the first time that an activated Src kinase requires the inactivation of Rho-mediated actin stress fibre assembly to induce its effects on actin disorganisation. Moreover, our work supports p190 as a strong candidate effector of v-Src-induced cytoskeletal disruption, most likely mediated by antagonism of the cellular function of Rho. (+info)Identification of a novel domain shared by putative components of the endocytic and cytoskeletal machinery. (8/10346)
We have identified a approximately 140 amino acid domain that is shared by a variety of proteins in budding and fission yeast, nematode, rat, mouse, frog, oat, and man. Typically, this domain is located within 20 residues of the N-terminus of the various proteins. The percent identity among the domains in the 12 proteins ranges from 42 to 93%, with 16 absolutely conserved residues: N-x(11-13)-V-x2-A-T-x(34-36)-R-x(7-8)-W-R-x3-K-x12-G-x-E-x15 -L-x11-12-D-x-G-R-x11-D-x7-R. Even though these proteins share little beyond their segment of homology, data are emerging that several of the proteins are involved in endocytosis and or regulation of cytoskeletal organization. We have named this protein segment the ENTH domain, for Epsin N-terminal Homology domain, and hypothesize that it is a candidate for binding specific ligands and/or enzymatic activity in the cell. (+info)The primary symptoms of Wiskott-Aldrich syndrome include:
1. Eczema and skin rashes
2. Immune system dysfunction, leading to recurrent infections
3. Bleeding disorders, including easy bruising and nosebleeds
4. Delayed development and growth retardation
5. Short stature
6. Poor muscle tone and coarse facial features
7. Heart defects, such as ventricular septal defects
8. Kidney disease or dysfunction
9. Increased risk of cancer, particularly lymphoma
Wiskott-Aldrich syndrome is diagnosed through a combination of clinical evaluation, laboratory tests, and genetic analysis. Treatment for the condition typically involves managing symptoms and preventing complications through medications, immunoglobulin replacement therapy, and other supportive measures.
The prognosis for individuals with Wiskott-Aldrich syndrome varies depending on the severity of their symptoms and the presence of any comorbidities. With appropriate medical care, many individuals with this condition can lead relatively normal lives, but they may require lifelong monitoring and treatment to manage their symptoms and prevent complications.
Cytoskeleton
Prokaryotic cytoskeleton
Cytoskeleton (journal)
Cytoskeleton regulator RNA
Activity-regulated cytoskeleton-associated protein
Cytoskeleton associated protein 2 like
Microtubule
Kinesin-like protein KIF11
Cortactin
LSP1
SCIN
Megakaryocyte
Spizellomyces punctatus
MAP7
BBS7
Familial amyloid neuropathy
Rong Li
Hugh Huxley
Schizosaccharomyces pombe
Shroom protein family
SORBS2
DYNLRB1
Polar filament
MreB
CEP89
MAP4
Centrin
Smooth muscle
MAP1A
MYO1C
Evolution of the cytoskeleton
Frontiers | Triggering Cation-Induced Contraction of Cytoskeleton Networks via Microfluidics
PAR-13-301: The Role of the Cytoskeleton in Cellular Aging (R21/R33)
Cell mechanics and the cytoskeleton - PubMed
From the ECM to the Cytoskeleton and Back: How Integrins Orchestrate T Cell Action
Cilia, Wnt signaling, and the cytoskeleton - PubMed
The mechanics and transport of the active cytoskeleton in biomimetic and living cellular systems | Biomimetic-Mechanics Project...
Mechanical stretching induces fibroblasts apoptosis through activating Piezo1 and then destroying actin cytoskeleton [Abstract]
Live Cell Imaging Of The Actin Cytoskeleton
Site-specific glycosylation regulates the form and function of the intermediate filament
cytoskeleton.
Control of the T Cell Cortex by the Septin Cytoskeleton
cytoskeleton
Activation of either ERK1/2 or ERK5 MAP kinase pathways can lead to disruption of the actin cytoskeleton | Journal of Cell...
Cytoskeleton: Function, Structure, Meaning & Diagram | AESL
Transcriptomics and proteomics show that selenium affects inflammation, cytoskeleton, and cancer pathways in human rectal...
Structure of cytoskeleton in excavates and euglenids | Stars Natur
Cytoskeleton, Transglutaminase and Gametophytic Self-Incompatibility in the Malinae (Rosaceae)
Effects of Plasma Membrane Cholesterol Level and Cytoskeleton F-Actin on Cell Protrusion Mechanics • MatTek Life Sciences
Cytoskeleton | Pancreapedia
The axonal cytoskeleton at the nanoscale | Webinars | Recursos | Nikon Instruments Inc.
Cytoskeleton - SCI Journal
Venkat - cytoskeleton-lab
Membranes, Cytoskeleton & ECM
Enzyme-activated intracellular drug delivery with tubule clay nanoformulation | Scientific Reports
cytoskeleton Archives - Dr. Cate
Cells with nuclei in blue, energy factories in green, and the actin cytoskeleton in red
Difference Between Cytoplasm and Cytoskeleton
Cytoskeleton: Description, Structure, and Function
Targeting the actin cytoskeleton1
- In contrast, by targeting the actin cytoskeleton. (nih.gov)
Reagents distributed2
- Cytoskeleton Inc Laboratories manufactures the cell cytoskeleton intermediate filaments reagents distributed by Genprice. (genediag.com)
- Cytoskeleton Inc Laboratories manufactures the protein fibers of the cytoskeleton reagents distributed by Genprice. (il-10.com)
Proteins8
- Our intriguing findings shed new light on how varying environmental conditions can dynamically tune the morphology of cytoskeleton networks and trigger active contraction without the use of motor proteins. (frontiersin.org)
- The cytoskeleton, a dynamic network of filamentous proteins, enables cells to maintain shape and structure while carrying out a wide range of processes such as cell proliferation, migration and division. (frontiersin.org)
- Active reorganization of cytoskeleton networks is typically driven by ATP-consuming motor proteins including myosin and kinesin. (frontiersin.org)
- Taken together these three networks are comprised of proteins which represent the major architectural building blocks of both the cytoplasm (classical cytoskeleton) and the nucleus (nucleoskeleton) of vertebrate cells. (nih.gov)
- The ability of a eukaryotic cell to resist deformation, to transport intracellular cargo and to change shape during movement depends on the cytoskeleton, an interconnected network of filamentous polymers and regulatory proteins. (nih.gov)
- As part of this process, microtubules , which are structural proteins that help make up the cell's cytoskeleton, reorganize the newly copied chromosomes into a dense, football-shaped spindle. (nih.gov)
- Mechanics of cells mainly come from the molecular interactions between actin filaments and diverse actin-binding proteins in the actin cytoskeleton. (purdue.edu)
- Multiple T3SS1 effector proteins target the actin cytoskeleton, directly or indirectly, to induce localized membrane ruffles on the cell surface. (nih.gov)
Make up the cell's1
- The cytoskeleton is a network of long fibers that make up the cell's structural framework. (medlineplus.gov)
Cytoskeletal4
- At the present time, remarkably little is known about the role of the cytoskeleton in the normal aging process, even though it is well established that there are numerous changes in cytoskeletal systems that have become the hallmarks of age-related disorders. (nih.gov)
- Of the many signaling pathways associated with primary cilia, the most extensively studied in association with the cytoskeleton and cytoskeletal rearrangements are both canonical and non-canonical Wnt pathways. (nih.gov)
- We also show that in Src -transformed cells inhibition of ERK1/2 signalling is not sufficient for reappearance of the actin cytoskeleton and that ERK5 activation contributes to cytoskeletal disruption by Src. (biologists.com)
- Several lines of indirect evidence, such as mutations or dysregulated expression of genes related to cytoskeleton , have suggested that cytoskeletal dynamics, a process essential for axons and dendrites development, is compromised in autism spectrum disorders (ASD). (bvsalud.org)
Microtubules5
- The dynamic morphology and mechanics of the cytoskeleton is determined by interacting networks of semiflexible actin filaments and rigid microtubules. (frontiersin.org)
- Two of the principle constituents of the cytoskeleton are thin semiflexible actin filaments, ∼7 nm wide with a persistence length of l p ∼ 10 μ m, and thicker rigid microtubules, ∼25 nm wide with l p ∼ 1 mm [ 1 , 2 ]. (frontiersin.org)
- Broadly defined, the cytoskeleton is a complex array of three major protein systems: microtubules, intermediate filaments and actin/microfilaments. (nih.gov)
- Like other eukaryotic cells, neurons have a cytoskeleton that consists of three main polymers: microtubules (green), intermediate filaments (purple) and actin filaments (red). (nih.gov)
- The cytoskeleton is made from protein structures called microtubules, made visible by fluorescently tagging a protein called doublecortin (orange). (nih.gov)
Protein3
- Evidence has accumulated that both the classical extracellular activated kinase (ERK) 1/2 mitogen activated protein (MAP) kinase pathway and the phosphoinositide 3-kinase (PI 3-kinase) pathway can contribute to alterations in the actin cytoskeleton. (biologists.com)
- Very little is known about the protein composition of protist's non-actin and non-tubulin cytoskeleton, i.e., the different types of intermediate and striated fibres. (stars-natur.cz)
- This allows imaging of the cytoskeleton structures and protein localization with unprecedented resolution. (stars-natur.cz)
Mechanics3
- A computational model can give additional information that is critical for understanding the mechanics of the cytoskeleton which in vitro assay cannot offer, such asthelocation or force of each molecule. (purdue.edu)
- Most of the previous models lack some mechanical details that could potentially be critical in the mechanics of the actin cytoskeleton. (purdue.edu)
- The model describes the detailed mechanics and dynamics, thus enabling the investigation of previously unexplored aspects of cytoskeleton mechanics. (purdue.edu)
Hoboken1
- Cytoskeleton (Hoboken). (nih.gov)
Filaments2
- Intermediate filaments (IF) are a major component of the metazoan cytoskeleton and are essential for normal cell morphology, motility, and signal transduction. (duke.edu)
- The Cell Cytoskeleton Intermediate Filaments reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. (genediag.com)
Eukaryotic2
Intracellular2
- Applications considering the effect of age on factors such as cytoskeleton structure and function, the impact of the cytoskeleton on intracellular organelle interactions, and signaling or regulatory molecules controlling cellular architecture are encouraged. (nih.gov)
- In addition, we show that the intracellular pathogen Chlamydia trachomatis, which remodels the host IF cytoskeleton during infection, requires specific vimentin glycosylation sites and O-GlcNAc transferase activity to maintain its replicative niche. (duke.edu)
Regulators2
Structures1
- Due to the complex geometry of the actin structures in non-muscle cells, it has not been well understood how the actin cytoskeleton generates force and remodels itself. (purdue.edu)
Regulates2
Cellular5
- The purpose of this FOA is to stimulate the development of innovative research strategies aimed at increasing the understanding of the molecular and cellular changes in the cytoskeleton that occur during the aging process. (nih.gov)
- Recent work has demonstrated that both internal and external physical forces can act through the cytoskeleton to affect local mechanical properties and cellular behaviour. (nih.gov)
- Although the cytoskeleton has historically been understood as the structural framework of the cell, the proper function of actin is also required for a diverse array of cellular pathways. (nih.gov)
- The collapse of these cellular processes manifests during aging and exposure to a myriad of stresses, which is in part due to the breakdown of the cytoskeleton under these conditions. (nih.gov)
- A major contributor to the lack of these essential studies is the lack of tools available for in vivo, live-cell imaging of the actin cytoskeleton in multi-cellular organisms. (nih.gov)
Cell9
- As the cilium is effectively a microtubular extension of the cytoskeleton, investigating connections between the cilium and the cytoskeleton provides greater insight into signaling and cell function. (nih.gov)
- Recent advances in organic chemical synthesis have facilitated the ultimate aim of producing small cell-permeable compounds which can efficiently label the actin cytoskeleton and track its dynamic properties 1-3 . (cytoskeleton.com)
- These alterations to the cytoskeleton can lead to increased cell motility through changes in actin dynamics and decreased cell adhesion. (biologists.com)
- This video, which took third place in the ASCB contest, shows the cytoskeleton of a frequently studied human breast cancer cell line. (nih.gov)
- To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Cytoskeleton Inc. Other Cell products are available in stock. (genediag.com)
- The famous neuroscientist C.S. Sherrington observed the cytoskeleton may act as the nervous system of single cell organisms. (metamia.com)
- Penrose and Hameroff speculated that the cytoskeleton is like a micro myofascial system, within each cell. (metamia.com)
- The cytoskeleton has several critical functions, including determining cell shape, participating in cell division, and allowing cells to move. (medlineplus.gov)
- Early in my postdoctoral career, I developed a system for robust, tissue-specific, live-cell imaging of the cytoskeleton in the muscle, intestine, and hypodermis of C. elegans, utilizing LifeAct fused to a fluorescent molecule. (nih.gov)
Molecular1
- Molecular architecture of the trypanosome cytoskeleton. (ox.ac.uk)
Occur1
- The mechanisms through which changes in the actin cytoskeleton occur in oncogenic transformation have been the focus of much investigation. (biologists.com)
Stem2
- Actin cytoskeleton dynamics in stem cells from autistic individuals. (bvsalud.org)
- Here we investigated the regulation of actin cytoskeleton dynamics in stem cells from human exfoliated deciduous teeth (SHEDs) of 13 ASD patients and 8 control individuals by inducing actin filament depolymerization and then measuing their reconstruction upon activation of the RhoGTPases Rac, Cdc42 or RhoA. (bvsalud.org)
Transformation3
- Oncogenic transformation often leads to the disruption of the actin cytoskeleton. (biologists.com)
- Many of the studies of the effects of oncogenes on the cytoskeleton have made use of chemical inhibitors of MEK1/2 but it is now clear that these inhibitors also inactivate MEK5 in the MEK5-ERK5 MAP kinase pathway raising the possibility that this pathway may also be involved in oncogenic transformation. (biologists.com)
- Altered regulation of the actin cytoskeleton is a common feature of malignant transformation. (biologists.com)
Mechanical1
- Li Y, Li L, Li B, Liao W, Liu T, Shen F, Hong L. Mechanical stretching induces fibroblasts apoptosis through activating Piezo1 and then destroying actin cytoskeleton. (medsci.org)
Functions1
- 17. Deletion of calponin 2 in macrophages alters cytoskeleton-based functions and attenuates the development of atherosclerosis. (nih.gov)
Cells2
- Based on these findings, Piezo1 connects the actin cytoskeleton to the apoptosis of hAVWFs cells, providing an idea for the clinical diagnosis and treatment of SUI. (medsci.org)
- However, no study has yet examined whether cytoskeleton dynamics is functionally altered in cells from ASD patients . (bvsalud.org)
Network1
- Yet, how cytoskeleton networks respond in real-time to changing ion concentrations, and how actin-microtubule interactions impact network response to these changing conditions remains unknown. (frontiersin.org)
Study2
- The aim of this study is to determine how Piezo1 and actin cytoskeleton are involved in the mechanized stretch (MS) induced apoptosis of human anterior vaginal wall fibroblasts (hAVWFs) and the mechanism. (medsci.org)
- This resubmission application for a Pathway to Independence Award (K99/R00) from the University of California (UC), Berkeley, CA, on behalf of the candidate Dr. Ryo Higuchi-Sanabria, proposes to study novel genes that are found to alter the chromatin state and lipid homeostasis in regulating the actin cytoskeleton. (nih.gov)
Results1
- This action results in the remodeling of the actin and microtubule cytoskeleton. (nih.gov)
Aging process1
- There is also interest in studying the role of the cytoskeleton in nuclear-cytoplasmic communications, and in spatio-temporal relationships during the aging process and in age-related diseases. (nih.gov)
Classical1
- Activation of the classical Ras-Raf-MEK1/2-ERK1/2 signalling cascade has been implicated in the effects of oncogenes such as Ras and Src on the cytoskeleton. (biologists.com)
Common1
- Interestingly, the breakdown of the cytoskeleton throughout age has been adopted as common knowledge in the field of aging biology, despite the lack of clear and direct evidence. (nih.gov)
Effect1
- However, the disassembly of the actin cytoskeleton suppressed the protective effect of Piezo1 silencing on MS. Based on these findings, Piezo1 connects the actin cytoskeleton to apoptosis of hAVWFs, providing new insight for the clinical diagnosis and treatment of SUI. (medsci.org)