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New melanocortin-like peptide of E. coli can suppress inflammation via the mammalian melanocortin-1 receptor (MC1R): possible endocrine-like function for microbes of the gut

E. coli releases a 33 amino acid peptide melanocortin-like peptide of E. coli (MECO-1) that is identical to the C-terminus of the E. coli elongation factor-G (EF-G) and has interesting similarities to two prominent mammalian melanocortin hormones, alpha-melanocyte-stimulating hormone (alpha-MSH) and...

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Detalles Bibliográficos
Autores principales: Qiang, Xiaoling, Liotta, Anthony S., Shiloach, Joseph, Gutierrez, J. C., Wang, Haichao, Ochani, Mahendar, Ochani, Kanta, Yang, Huan, Rabin, Aviva, LeRoith, Derek, Lesniak, Maxine A., Böhm, Markus, Maaser, Christian, Kannengiesser, Klaus, Donowitz, Mark, Rabizadeh, Shervin, Czura, Christopher J., Tracey, Kevin J., Westlake, Mark, Zarfeshani, Aida, Mehdi, Syed F., Danoff, Ann, Ge, Xueliang, Sanyal, Suparna, Schwartz, Gary J., Roth, Jesse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684143/
https://www.ncbi.nlm.nih.gov/pubmed/29152323
http://dx.doi.org/10.1038/s41522-017-0039-9
Descripción
Sumario:E. coli releases a 33 amino acid peptide melanocortin-like peptide of E. coli (MECO-1) that is identical to the C-terminus of the E. coli elongation factor-G (EF-G) and has interesting similarities to two prominent mammalian melanocortin hormones, alpha-melanocyte-stimulating hormone (alpha-MSH) and adrenocorticotropin (ACTH). Note that MECO-1 lacks HFRW, the common pharmacophore of the known mammalian melanocortin peptides. MECO-1 and the two hormones were equally effective in severely blunting release of cytokines (HMGB1 and TNF) from macrophage-like cells in response to (i) endotoxin (lipopolysaccharide) or (ii) pro-inflammatory cytokine HMGB-1. The in vitro anti-inflammatoty effects of MECO-1 and of alpha-MSH were abrogated by (i) antibody against melanocortin-1 receptor (MC1R) and by (ii) agouti, an endogenous inverse agonist of MC1R. In vivo MECO-1 was even more potent than alpha-MSH in rescuing mice from death due to (i) lethal doses of LPS endotoxin or (ii) cecal ligation and puncture, models of sterile and infectious sepsis, respectively.