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View more ,PURPOSE: Artificial materials such as dental implants are at risk of bacterial contamination in the oral cavity. Human beta defensins (HBDs), small cationic antimicrobial peptides that exert a broad-spectrum antibacterial function at epithelial surfaces and within some mesenchymal tissues, could probably help to reduce such contamination. HBDs also have protective immunomodulatory effects and have been reported to promote bone remodeling. The aim of this study, therefore, was to investigate the influence of recombinant HBD-2 on the proliferation and survival of cells in culture. MATERIALS AND METHODS: Human mesenchymal stem cells (hMSCs), human osteoblasts, human keratinocytes (control), and the HeLa cancer cell line (control) were incubated with recombinant HBD-2 (1, 5, 10, or 20 姯mL). Cell proliferation and cytotoxicity were evaluated via a water-soluble tetrazolium salt (WST-1) and lactate dehydrogenase assays, respectively. RESULTS: HBD-2 was not toxic in any tested ...

Beta defensins are a family of mammalian defensins. The beta defensins are antimicrobial peptides implicated in the resistance of epithelial surfaces to microbial colonization. Defensins are 2-6 kDa, cationic, microbicidal peptides active against many Gram-negative and Gram-positive bacteria, fungi, and enveloped viruses, containing three pairs of intramolecular disulfide bonds. On the basis of their size and pattern of disulfide bonding, mammalian defensins are classified into alpha, beta and theta categories. Every mammalian species explored thus far has beta-defensins. In cows, as many as 13 beta-defensins exist in neutrophils. However, in other species, beta-defensins are more often produced by epithelial cells lining various organs (e.g. the epidermis, bronchial tree and genitourinary tract. Human, rabbit and guinea-pig beta-defensins, as well as human beta-defensin-2 (hBD2), induce the activation and degranulation of mast cells, resulting in the release of histamine and prostaglandin D2. ...

Although, the human epithelium is constantly challenged by a broad spectrum of microorganisms, invasive infections are rather rare. Recent findings suggest the expression of antimicrobial peptides by

TY - JOUR. T1 - Rapid sequence divergence in mammalian beta-defensins by adaptive evolution. AU - Maxwell, A I. AU - Morrison, G M. AU - Dorin, J R. PY - 2003. Y1 - 2003. N2 - beta-Defensin genes encode broad spectrum antimicrobial cationic peptides. We have analysed the largest murine and human clusters of these genes, which localise to mouse and human chromosome 8. Using hidden Markov models, we identified novel mouse and human beta-defensin genes. We subsequently found full-length expressed transcripts for these novel genes. Expression in the mouse was high in brain and reproductive tissues. Fourteen murine beta-defensins could be grouped into two clear sub-groups by virtue of their position and high signal sequence (exon 1 encoded) identity. In contrast, there was a very low level of sequence conservation in the exon 2 region encoding the mature antimicrobial peptide. Evolutionary analysis revealed strong evidence that following gene duplication, exon 1 and surrounding non-coding DNA show ...

Myeloid Elf-1 like factor (MEF) is an ETS protein, which activates the promoters of granulocyte macrophage colony-stimulating factor, interleukin-3, lysozyme, human beta defensin-2 and perforin. In spite

The solution structure is reported for bovine neutrophil beta-defensin-12 (BNBD-12), a member of the beta-defensin family of antimicrobial peptides. Structural constraints in the form of proton-proton distances, dihedral angles, and hydrogen bond constraints were derived from two-dimensional, homonu …

The authors characterize the recombinant human beta-defensin DEFB114 peptide, demonstrating its anti-microbial potential, lipopolysaccharide (LPS) binding and neutralization, and anti-inflammatory effects in vitro and in vivo. Data suggest that DEFB114 could also protect human sperm from motility loss when challenged with LPS. Affinity measurements of interaction between LPS and DEFB114 were performed using the Octet system. Purified DEFB114 was biotinylated and loaded onto Streptavidin biosensors, followed by association/dissociation with purified LPS.

1BNB: Solution structure of bovine neutrophil beta-defensin-12: the peptide fold of the beta-defensins is identical to that of the classical defensins.

International Journal of Peptides is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of peptide research.

Background: Smoking increases the susceptibility to pulmonary infection and is a risk factor for the development of chronic obstructive pulmonary disease (COPD). We postulated that cigarette smoke suppresses the activation of the innate immune system in response to bacterial infection. Methods: With sensitive ex-vivo analysis we measured the level of the endogenous antibiotic peptide human beta-defensin-2 in pharyngeal washing fluids and sputum of patients with community acquired pneumonia. The regulation of antibacterial host defense molecules was studied in vitro. The effect of cigarette smoke on the antibacterial activity of differentiated airway epithelium and the expression of host defense molecules was studied in an infection model in vitro. Results: Current or former smoking was associated with significantly reduced hBD-2 levels in pharyngeal washing fluid and sputum from patients with acute pneumonia. Exposure of airway epithelium to smoke in vitro inhibited the induction of hBD-2 by ...

Background: Mycobacterium tuberculosis (Mtb), a pathogenic acid-fast bacterium causes ten million infections and two million deaths per year. Multidrug resistance of Mtb has been in part attributed to its lipid rich cell wall and tendency to aggregate. Mucosal surfaces in the respiratory tract secrete antimicrobial peptides including human beta-defensins (HBD) which typically exert their effects at low μM concentrations. HBD2 has been thought to primarily act as chemoattractant. However, considering its association with lipid membranes direct activity against Mtb is conceivable. Objective: Using Mycobacterium smegmatis (Ms) as a model organism for Mtb, this study aimed to establish a protocol to homogenize Ms and test the effectiveness of HBD-2 against Ms. Methods: Ms was grown for 48 h in 7H9 medium, adjusted to McF 0.5, sonicated for 3, 5, and 9 rounds of five second durations, and diluted 1:50 in 7H9 media. Aliquots in five replicates were further incubated in a microtiter plate for 48 h and

AMP play an important role in the innate immune response against infections. Two major classes of AMP have been identified: the beta defensins (HBD) (Harder 1997) and cathelicidins (LL-37) (Gallo 2002). AMP have been shown to have antibacterial activities against S. aureus (Ong 2002) and antiviral activity against vaccinia virus (VV) (Howell 2004).. The skin of AD patients is characterized by a deficiency in AMP, which may account for their propensity to skin infections (Ong 2002). This AMP deficiency is believed to be due to an increase in Th2 cytokines, IL-4 and IL-13, expression (Ong 2002), as well as an increase of IL-10 expression (Howell 2005). Other cytokines known to affect AMP expression are TNF-alpha (TNFa), IL-6, IL-1 and interferon-gamma (IFN-g). These cytokines induce the expression of AMP (Erdag 2002, Liu 2002, Ong 2002, Nomura 2003). However, negligible levels of TNF-a and IFN-g have been shown in AD skin possibly due to their downregulation by Th2 cytokines (Nomura 2003). ...

Hyperbranched polyimide-silica hybrids (HBPI-silica HBDs) and hyperbranched polyimide-silica composites (HBPI-silica CPTs) were prepared, and their general and gas transport properties were investigated to clarify the effect of silica sources and preparation methods. HBPI-silica HBDs and HBPI-silica CPTs were synthesized by two-step polymerization of A2 + B3 monomer system via polyamic acid as precursor, followed by hybridizing or blending silica sources. Silica components were incorporated by the sol-gel reaction with tetramethoxysilane (TMOS) or the addition of colloidal silica. In HBPI-silica HBDs, the aggregation of silica components is controlled because of the high affinity of HBPI and silica caused by the formation of covalent bonds between HBPI and silica. Consequently, HBPI-silica HBDs had good film formability, transparency, and mechanical properties compared with HBPI-silica CPTs. HBPI-silica HBD and CPT membranes prepared via the sol-gel reaction with TMOS showed specific gas permeabilities

Hyperbranched polyimide-silica hybrids (HBPI-silica HBDs) and hyperbranched polyimide-silica composites (HBPI-silica CPTs) were prepared, and their general and gas transport properties were investigated to clarify the effect of silica sources and preparation methods. HBPI-silica HBDs and HBPI-silica CPTs were synthesized by two-step polymerization of A2 + B3 monomer system via polyamic acid as precursor, followed by hybridizing or blending silica sources. Silica components were incorporated by the sol-gel reaction with tetramethoxysilane (TMOS) or the addition of colloidal silica. In HBPI-silica HBDs, the aggregation of silica components is controlled because of the high affinity of HBPI and silica caused by the formation of covalent bonds between HBPI and silica. Consequently, HBPI-silica HBDs had good film formability, transparency, and mechanical properties compared with HBPI-silica CPTs. HBPI-silica HBD and CPT membranes prepared via the sol-gel reaction with TMOS showed specific gas permeabilities

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Defensins (alpha and beta) are cationic peptides with a broad spectrum of antimicrobial activity that comprise an important arm of the innate immune system. The alpha-defensins which include NP-1, NP-2 and NP-3, are distinguished from the beta-defensins by the pairing of their three disulfide bonds. In addition to antimicrobial activity, NP-1 exhibits chemotactic activity on dendritic cells. NP-1 is expressed as the C-terminal portion of an inactive precursor protein, which also contains a 19 amino acid N-terminal signal sequence and a 45 amino acid polypeptide. NP-1 contains a six-cysteine motif that forms three intra-molecular disulfide bonds. Recombinant human NP-1 is a 3.4 kDa protein containing 30 amino acid residues ...

GPR29 [ENSP00000343952]. Chemokine (C-C motif) receptor 6; Receptor for the C-C type chemokine CCL20. Binds to CCL20 and subsequently transduces a signal by increasing the intracellular calcium ion levels. Although CCL20 is its major ligand it can also act as a receptor for non-chemokine ligands such as beta-defensins. Binds to defensin DEFB1 leading to increase in intracellular calcium ions and cAMP levels. Its binding to DEFB1 is essential for the function of DEFB1 in regulating sperm motility and bactericidal activity. Binds to defensins DEFB4 and DEFB4A/B and mediates their chemotactic effects. The ligand-receptor pair CCL20-CCR6 is responsible for the chemotaxis of dendritic cells (DC), effector/ memory T-cells and B-cells and plays an important role at skin and mucosal surfaces under homeostatic and inflammatory conditions, as well as in pathology, including cancer and various autoimmune diseases. CCR6-mediated signals are essential for immune responses to microbes in the intestinal mucosa ...

Creative Peptides offers Beta-defensin 2 for your research. We also provide custom peptide synthesis, process development, GMP manufacturing.

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DEFB119 - DEFB119 (untagged)-Human defensin, beta 119 (DEFB119), transcript variant 3 available for purchase from OriGene - Your Gene Company.

Complete information for DEFB129 gene (Protein Coding), Defensin Beta 129, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Complete information for DEFB126 gene (Protein Coding), Defensin Beta 126, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

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Human beta defensins (hBDs) are small cationic peptides, expressed in mucosal epithelia and important agents of innate immunity, act as antimicrobial and chemotactic agents at mucosal barriers. In this perspective, we present evidence supporting a novel strategy by which the oral bacterium Fusobacterium nucleatum induces hBDs and other antimicrobial peptides (AMPs) in normal human oral epithelial cells and thereby protects them from other microbial pathogens. The findings stress (1) the physiological importance of hBDs, (2) that this strategy may be a mechanism that contributes to homeostasis and health in body sites constantly challenged with bacteria and (3) that novel properties identified in commensal bacteria could, one day, be harnessed as new probiotic strategies to combat colonization of opportunistic pathogens. With that in mind, we highlight and review the discovery and characterization of a novel lipo-protein, FAD-I (Fusobacterium Associated Defensin Inducer) associated with the outer

Hata, T., Kotol, P., Boguniewicz, M., Taylor, P., Paik, A., Jackson, M., ... et al, . U. (2011). History of eczema herpeticum is associated with the inability to induce human beta-defensin (HBD)-2, HBD-3 and cathelicidin in the skin of patients with atopic dermatitis. British Journal of Dermatology, 163(3), 659 - 661 ...

Beta-defensin 106 is a protein that in humans is encoded by the DEFB106A gene. Defensins form a family of microbicidal and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 106, DEFB106A and DEFB106B, in head-to-head orientation. This gene, DEFB106A, represents the more centromeric copy. The purified DEFB106 showed antimicrobial activity against Escherichia coli, Candida albicans and Staphylococcus aureus. GRCh38: Ensembl release 89: ENSG00000186579 - Ensembl, May 2017 Human PubMed Reference:. Schutte BC, Mitros JP, Bartlett JA, Walters JD, Jia HP, Welsh MJ, Casavant TL, McCray PB Jr (Feb 2002). Discovery of ...

RefSeq Summary (NM_001037668): Defensins form a family of antimicrobial and cytotoxic peptides made by neutrophils. Defensins are short, processed peptide molecules that are classified by structure into three groups: alpha-defensins, beta-defensins and theta-defensins. All beta-defensin genes are densely clustered in four to five syntenic chromosomal regions. Chromosome 8p23 contains at least two copies of the duplicated beta-defensin cluster. This duplication results in two identical copies of defensin, beta 107, DEFB107A and DEFB107B, in tail-to-tail orientation. This gene, DEFB107A, represents the more centromeric copy. [provided by RefSeq, Oct 2014 ...

Defensin-1 was prepared by heterologous expression in Escherichia coli. We showed that different types of honey (manuka and honeydew) were able to significantly reduced cell viability of wound pathogens (S. aureus, S. agalactiae and P. aeruginosa) in polymicrobial biofilm. None of the tested honeys showed the ability to eradicate E. faecalis in biofilm. In addition, recombinant defensin-1 successfully reduced the viability of S. aureus and P. aeruginosa cells within established polymicrobial biofilm after 24 and 48 hours of treatment. Interestingly, recombinant defensin-1 did not affect the viability of S. agalactiae cells within the biofilm whereas both natural honeys significantly reduced the viable bacteria. Although E. faecalis was highly resistant to defensin-1, defensin-1 significantly affected biofilm formation of E. faecalis and S. agalactiae after 24 hours of treatment, most likely through the inhibiting its extracellular polymeric substances production ...

Defensins are antimicrobial peptides that play an important role in the innate immune response in the intestine. Up to date, only one ß-defensin (pBD-1), has been described in pig, which was found to be expressed at low levels in the intestine. We set-up a quantitative PCR method to detect the gene expression of pBD-1 and a newly discovered porcine ß-defensin, pBD-2. Expression of pBD-1 mRNA increased from the proximal to the distal part of the intestine whereas pBD-2 expression decreased. The main gene expression sites for pBD-2 were kidney and liver, whereas pBD-1 was mainly expressed in tongue. The porcine small intestinal segment perfusion (SISP) technique was used to investigate effects of Salmonella typhimurium DT104 on intestinal morphology and pBD-1 and pBD-2 mRNA levels in vivo. The early responses were studied 2, 4 and 8 h post-infection in four separate jejunal and ileal segments. Immunohistochemistry showed invasion of the mucosa by Salmonella and changes in intestinal morphology. ...

Research Opportunities: We encourage the fellow to participate in at least two clinical research projects throughout the year (in conjunction with a resident and Case Western medical student). There are a myriad of opportunities to choose from. The fellow has the ability to present any successfully submitted research projects at the AHNS spring meeting. This is fully supported by the department.. Involvement in the Case Head and Neck Research Collaborative. Clinical: Besides retrospective studies, the fellow can work with the clinical trial unit (team, CTU) to better understand the role head and neck surgeons play in institutional and national clinical trials and how to integrate this important aspect of research into their future practice.. Molecular Biology: A collaboration between Drs. Ge Jin, PhD, Aaron Weinberg, PhD of Case Western Reserve University and Chad Zender, MD obtained an R01 to study innate immune molecules (human beta defensins) role in the development of head and neck cancer. ...

α-Defensins are abundant antimicrobial peptides in polymorphonuclear leukocytes and play an important role in innate immunity. We have previously shown that α-defensin-1 can inhibit HIV-1 replication following viral entry. Here we examined the molecular mechanism(s) of α-defensin-1-mediated HIV-1 inhibition. α-Defensin-1 had a direct effect on HIV-1 virions at a low MOI in the absence of serum. The direct effect on HIV-1 virions was abolished by the presence of serum or an increase in virus particles. Studying the kinetics of the HIV life cycle revealed that α-defensin-1 inhibited steps following reverse transcription and integration. Analysis of PKC phosphorylation in primary CD4+ T cells in response to α-defensin-1 indicated that α-defensin-1 inhibited PKC activity. Pretreatment of infected CD4+ T cells with a PKC activator, bryostatin 1, partially reversed α-defensin-1-mediated HIV inhibition. Like α-defensin-1, the PKC isoform-selective inhibitor Go6976 blocked HIV-1 infection in a ...

To identify the component responsible for inducing MMP-9 production, RJ extract was fractionated using C18 RP-HPLC. In fractions exhibiting stimulatory activity, we immunochemically detected the bee-derived antibacterial peptide, defensin-1. Defensin-1 was cloned, and recombinant peptide was produced in a baculoviral expression system. Defensin-1 stimulated MMP-9 secretion from keratinocytes and increased keratinocyte migration and wound closure in vitro. In addition, defensin-1 promoted re-epithelisation and wound closure in uninfected excision wounds ...

TY - JOUR. T1 - Ageing and free-living daily physical activity effects on salivary beta-defensin 2 secretion. AU - Shimizu, Kazuhiro. AU - Hanaoka, Yukichi. AU - Akama, Takao. AU - Kono, Ichiro. N1 - Funding Information: This work was supported by the Science Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan [grant numbers 21700705 and 25750358 to Kazuhiro Shimizu]. Publisher Copyright: © 2016 Informa UK Limited, trading as Taylor & Francis Group.. PY - 2017/4/3. Y1 - 2017/4/3. N2 - This study examined ageing and free-living daily physical activity effects on salivary human beta-defensin 2 (hBD2). A total of 168 healthy elderly and 26 healthy young volunteers underwent saliva sampling. Free-living step count, energy expenditure and activity durations at specific intensity levels (inactive, light, moderate and vigorous) were evaluated. The results show significantly lower salivary hBD2 secretion rates for elderly than for young participants (P , 0.05). ...

Fitschen-Oestern S, Weuster M, Lippross S et al.. Department of Trauma Surgery, University Medical Center of Schleswig-Holstein, Campus Kiel, Arnold-Heller-Strasse 3, 24105, Kiel, Germany.. BMC musculoskeletal disorders. Mar 2017.. Human-beta defensins (HBD) belong to the family of acute phase peptides and hold a broad antimicrobial spectrum that includes gram-positive and gram-negative bacteria. HBD are up-regulated after severe injuries but the source of posttraumatic HBD expression has not been focused on before. In the current study we analysed the role of liver tissue in expression of HBD after multiple trauma in human and mice.HBD-2 expression has been detected in plasma samples of 32 multiple trauma patients (ISS > 16) over 14 days after trauma by ELISA. To investigate major sources of HBD-2, its expression and regulation in plasma samples, polymorphonuclear neutrophils (PMN) and human tissue samples of liver and skin were analysed by ELISA. As liver samples of trauma patients are hard to ...

Antimicrobial peptides of the beta-defensin family are expressed in all human epithelial tissues tested to date and have recently been the subject of vigorous investigation. Their localization and characteristics support the hypothesis that these peptides play a role in mucosal and skin defense. The …

INTRODUCTION. Defensins and cathelicidins constitute the two major groups of antimicrobial peptides in most mammalian species. The most abundant group of antimicrobial peptides is comprised by the α-, β- and θ-defensins.[alpha, beta, theta (circle w/horizontal line)] Mammalian defensins are endogenous cysteine-rich peptide antibiotics classically produced either by epithelial cells of the respiratory, urogenital and digestive tracts, or by circulating cells including granulocytes and macrophages. More recently, however, β-defensins have also been identified in the heart of different species. BETA-DEFENSINS. β-defensins are small (3.5-4.5 kDa) highly basic cationic peptides. These peptides are ancient and universal molecules of innate immunity with functions extending far beyond simple antibiotics, including anti-tumor and mitogenic activity, as well as immunomodulation and signal transduction characteristics. The overall effectiveness of an innate immunity based host defense is shown by the ...

This application is in response to PA-09-164 (NIH Exploratory Developmental Research Grant Program). Given the high rate of hospital-acquired infection in criti...

PURPOSE Antimicrobial peptides (AMPs) are cationic host defense peptides with microbicidal and cell-signaling properties. They show promise as potential therapeutic agents. In the present study, a beta-defensin AMP gene was isolated from the ocular surface for the first time, and its expression was characterized in the presence of ocular inflammation and/or infection. METHODS Total RNA was obtained from impression cytology samples of the conjunctiva and cornea of normal patients and of those with bacterial, viral, acanthamoeba, or dry eye disease. The expression of the beta-defensin AMP DEFB-109 was determined by using reverse transcription-polymerase chain reaction (RT-PCR). Relative quantification of the gene in the various groups was performed by means of real-time PCR. RESULTS DEFB-109 was constitutively expressed in all samples. The gene showed significantly decreased expression in the presence of all types of inflammation/infection. Reduced expression featured most prominently in acanthamoeba

Responding to a test challenge: I clearly stated that The ciliary epithelial cells produce antimicrobial peptides like beta-defensins. On page 6 it states that the Primary granules in neutrophils contain myeloperoxidase enzyme, lysozyme and alpha-defensins. The statement indicating that neutrophils produce alpha-defensins is again reiterated in the same page. I appreciate the fact that you did a literature search and found an article from 1995 demonstrating defensin production from macrophages. This is an outdated report. There are more than 292 research articles reporting the production of alpha-defensins by neutrophils. I have pasted the PubMed link below. The challenge is denied. ...

Purified Recombinant Human DEFB110 Protein, GST-tagged from Creative Biomart. Recombinant Human DEFB110 Protein, GST-tagged can be used for research.

摘要 旨在研究氨基酸平衡低蛋白质日粮对育肥猪肠道抗菌肽与微生物区系的影响。将20头（60±2.5）kg的育肥猪（杜×长×大）随机分为4个处理：14.0% CP日粮（14.0% CP），添加Glu、Lys、Met、Thr和Trp的12.5% CP日粮（12.5% CP），添加Glu、Lys、Met、Thr和Trp的11.0% CP日粮（11.0% CP），添加Glu、Lys、Met、Thr、Trp和BCAA（Val、Ile、Leu）的11.0% CP日粮（11.0% CP+BCAA）。每个处理5个重复，每个重复1头猪。试验分为5 d预试期和30 d正试期。结果表明：（1）尿液尿素氮和尿酸含量随日粮蛋白质水平降低而显著降低（P,0.05）；（2）低蛋白质水平日粮显著降低空肠黏膜、回肠黏膜β-defensin-2水平和ANG1、ANG4 mRNA表达水平（P,0.05）；（3）不同蛋白质水平日粮对部分回肠、直肠食糜微生物氨基酸组成有显著影响（P,0.05）；（4）与14.0% CP组相比，12.5% CP组Observed species显著提高（P,0.05），11.0% ...

Defensins (alpha and beta) are cationic peptides with a broad spectrum of antimicrobial activity that comprise an important arm of the innate

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Polyclonal antibody for DEFB1 detection. Host: Rabbit.Size: 100μg/vial. Tested applications: IHC-P. Reactive species: Human. DEFB1 information: Molecular Weight: 7420 MW; Subcellular Localization: Secreted; Tissue Specificity: Plasma.

Cationic antimicrobial peptides (CAPs) are a promising new class of natural-source drugs that may avoid the shortcomings of conventional chemotherapy because certain CAPs exhibit selective cytotoxicity against a broad spectrum of human ...