The neuroendocrine peptide catestatin is a cutaneous antimicrobial and induced in the skin after injury.
暂无分享,去创建一个
D. O'Connor | P. Elias | S. Mahata | L. Taupenot | I. Niesman | R. Gallo | B. López-Garcı́a | Katherine A. Radek | K. Radek | M. Hupe | B. López-García
[1] J. Wagner,et al. CGRP, PACAP, and VIP modulate Langerhans cell function by inhibiting NF-kappaB activation. , 2007, The Journal of investigative dermatology.
[2] Y. Helfrich,et al. Injury enhances TLR2 function and antimicrobial peptide expression through a vitamin D-dependent mechanism. , 2007, The Journal of clinical investigation.
[3] P. Elias,et al. Transepidermal water loss reflects permeability barrier status: validation in human and rodent in vivo and ex vivo models , 2006, Experimental dermatology.
[4] T. Hökfelt,et al. The antimicrobial peptide cathelicidin protects the urinary tract against invasive bacterial infection , 2006, Nature Medicine.
[5] D. Atanackovic,et al. Physiology and Pharmacology of Temperature Regulation Patients with solid tumors treated with high-temperature whole body hyperthermia show a redistribution of naive / memory T-cell subtypes , 2006 .
[6] V. Nizet,et al. The mammalian ionic environment dictates microbial susceptibility to antimicrobial defense peptides , 2006, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[7] F. Dhabhar,et al. Stress as an endogenous adjuvant: augmentation of the immunization phase of cell-mediated immunity. , 2005, International immunology.
[8] D. O'Connor,et al. Hypertension from targeted ablation of chromogranin A can be rescued by the human ortholog. , 2005, The Journal of clinical investigation.
[9] M. Kagnoff,et al. Cathelicidin Mediates Innate Intestinal Defense against Colonization with Epithelial Adherent Bacterial Pathogens1 , 2005, The Journal of Immunology.
[10] C. Haglund,et al. Neuroendocrine differentiation in primary Merkel cell carcinoma--possible prognostic significance. , 2005, Anticancer research.
[11] A. Di Nardo,et al. Keratinocytes store the antimicrobial peptide cathelicidin in lamellar bodies. , 2005, The Journal of investigative dermatology.
[12] K. Helle,et al. New antimicrobial activity for the catecholamine release-inhibitory peptide from chromogranin A , 2005, Cellular and Molecular Life Sciences CMLS.
[13] N. McCallum,et al. Reduced Content of Lysyl-Phosphatidylglycerol in the Cytoplasmic Membrane Affects Susceptibility to Moenomycin, as Well as Vancomycin, Gentamicin, and Antimicrobial Peptides, in Staphylococcus aureus , 2004, Antimicrobial Agents and Chemotherapy.
[14] D. O'Connor,et al. The Catecholamine Release-Inhibitory “Catestatin” Fragment of Chromogranin A: Naturally Occurring Human Variants with Different Potencies for Multiple Chromaffin Cell Nicotinic Cholinergic Responses , 2004, Molecular Pharmacology.
[15] D. O'Connor,et al. Conformational preferences and activities of peptides from the catecholamine release-inhibitory (catestatin) region of chromogranin A , 2004, Regulatory Peptides.
[16] V. Nizet,et al. Antimicrobial peptides and the skin , 2004, Expert opinion on biological therapy.
[17] A. Villa,et al. Chromogranin A protects vessels against tumor necrosis factor α‐induced vascular leakage , 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[18] R. Gallo,et al. Postsecretory Processing Generates Multiple Cathelicidins for Enhanced Topical Antimicrobial Defense1 , 2004, The Journal of Immunology.
[19] Douglas W. Smith,et al. Both rare and common polymorphisms contribute functional variation at CHGA, a regulator of catecholamine physiology. , 2004, American journal of human genetics.
[20] K. Kurokawa,et al. Characterization of the Staphylococcus aureus mprF gene, involved in lysinylation of phosphatidylglycerol. , 2004, Microbiology.
[21] D. Aunis,et al. Innate immunity: involvement of new neuropeptides. , 2003, Trends in microbiology.
[22] P. Bradford,et al. Inactivation of mprF affects vancomycin susceptibility in Staphylococcus aureus. , 2003, Biochimica et biophysica acta.
[23] D. Aunis,et al. Antimicrobial Chromogranins and Proenkephalin‐A—Derived Peptides , 2003 .
[24] J. C. Tony. The chromogranin-secretogranin family. , 2003, The New England journal of medicine.
[25] D. Aunis,et al. Antimicrobial chromogranins and proenkephalin-A-derived peptides: Antibacterial and antifungal activities of chromogranins and proenkephalin-A-derived peptides. , 2003, Annals of the New York Academy of Sciences.
[26] Tomas Ganz,et al. Endogenous antimicrobial peptides and skin infections in atopic dermatitis. , 2002, The New England journal of medicine.
[27] D. O'Connor,et al. Early decline in the catecholamine release-inhibitory peptide catestatin in humans at genetic risk of hypertension. , 2002, Journal of hypertension.
[28] Robert E W Hancock,et al. Cationic peptides: distribution and mechanisms of resistance. , 2002, Current pharmaceutical design.
[29] Takaaki Ohtake,et al. Innate antimicrobial peptide protects the skin from invasive bacterial infection , 2001, Nature.
[30] D. O'Connor,et al. Proteolytic Cleavage of Chromogranin A (CgA) by Plasmin , 2001, The Journal of Biological Chemistry.
[31] V. Nizet,et al. Cutaneous injury induces the release of cathelicidin anti-microbial peptides active against group A Streptococcus. , 2001, The Journal of investigative dermatology.
[32] Michael Otto,et al. Staphylococcus aureus Resistance to Human Defensins and Evasion of Neutrophil Killing via the Novel Virulence Factor Mprf Is Based on Modification of Membrane Lipids with l-Lysine , 2001, The Journal of experimental medicine.
[33] J. Schröder,et al. Isolation and Characterization of Human β-Defensin-3, a Novel Human Inducible Peptide Antibiotic* , 2001, The Journal of Biological Chemistry.
[34] D. Aunis,et al. Antibacterial and Antifungal Activities of Vasostatin-1, the N-terminal Fragment of Chromogranin A* , 2000, The Journal of Biological Chemistry.
[35] J. M. Lipton,et al. Antimicrobial effects of α‐MSH peptides , 2000 .
[36] J. M. Lipton,et al. Antimicrobial effects of alpha-MSH peptides. , 2000, Journal of Leukocyte Biology.
[37] D. Torpy,et al. Stress, Corticotropin‐Releasing Hormone, Glucocorticoids, and the Immune/Inflammatory Response: Acute and Chronic Effects a , 1999, Annals of the New York Academy of Sciences.
[38] S. Yoshikawa,et al. Enhancement of Antimicrobial Activity of Neuropeptide Y by N-Terminal Truncation , 1998, Antimicrobial Agents and Chemotherapy.
[39] R. Bals,et al. The peptide antibiotic LL-37/hCAP-18 is expressed in epithelia of the human lung where it has broad antimicrobial activity at the airway surface. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[40] D. O'Connor,et al. Mechanism of cardiovascular actions of the chromogranin A fragment catestatin in vivo , 1998, Peptides.
[41] D. Low,et al. Reduced Virulence of Group A Streptococcal Tn916 Mutants That Do Not Produce Streptolysin S , 1998, Infection and Immunity.
[42] D. O'Connor,et al. A novel, catecholamine release-inhibitory peptide from chromogranin A: autocrine control of nicotinic cholinergic-stimulated exocytosis. , 1998, Advances in pharmacology.
[43] R. Siebert,et al. Mapping of the gene encoding human beta-defensin-2 (DEFB2) to chromosome region 8p22-p23.1. , 1997, Genomics.
[44] D. O'Connor,et al. Novel autocrine feedback control of catecholamine release. A discrete chromogranin a fragment is a noncompetitive nicotinic cholinergic antagonist. , 1997, The Journal of clinical investigation.
[45] M. Ackermann,et al. Epithelial antibiotic induced in states of disease. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[46] G. Trinchieri,et al. Calcitonin gene-related peptide inhibits proliferation and antigen presentation by human peripheral blood mononuclear cells: effects on B7, interleukin 10, and interleukin 12. , 1997, The Journal of investigative dermatology.
[47] G. Trinchieri,et al. Calcitonin gene-related peptide inhibits proliferation and antigen presentation by human peripheral blood mononuclear cells: effects on B7, interleukin 10, and interleukin 12. , 1997, Journal of Investigative Dermatology.
[48] D. O'Connor,et al. Chromogranin A processing and secretion: specific role of endogenous and exogenous prohormone convertases in the regulated secretory pathway. , 1996, The Journal of clinical investigation.
[49] A. Laslop,et al. Secretogranin II: Molecular properties, regulation of biosynthesis and processing to the neuropeptide secretoneurin , 1995, Progress in Neurobiology.
[50] M. Claeys,et al. Posttranslational processing of proenkephalins and chromogranins/secretogranins , 1993, Neurochemistry International.
[51] P. Elias,et al. Cutaneous barrier perturbation stimulates cytokine production in the epidermis of mice. , 1992, The Journal of clinical investigation.
[52] D. O'Connor,et al. Chromogranin A. Storage and release in hypertension. , 1990, Hypertension.
[53] D. O'Connor,et al. Immunological studies on the occurrence and properties of chromogranin A and B and secretogranin II in endocrine tumors. , 1988, The American journal of surgical pathology.
[54] W. Huttner,et al. Tyrosine-O-sulfated proteins of PC12 pheochromocytoma cells and their sulfation by a tyrosylprotein sulfotransferase. , 1983, The Journal of biological chemistry.
[55] D. O'Connor. Chromogranin: widespread immunoreactivity in polypeptide hormone producing tissues and in serum , 1983, Regulatory Peptides.
[56] K. Helle,et al. The release of protein from the stimulated adrenal medulla. , 1965, The Biochemical journal.