TY - JOUR
T1 - New melanocortin-like peptide of E. coli can suppress inflammation via the mammalian melanocortin-1 receptor (MC1R)
T2 - Possible endocrine-like function for microbes of the gut
AU - Qiang, Xiaoling
AU - Liotta, Anthony S.
AU - Shiloach, Joseph
AU - Gutierrez, J. C.
AU - Wang, Haichao
AU - Ochani, Mahendar
AU - Ochani, Kanta
AU - Yang, Huan
AU - Rabin, Aviva
AU - Leroith, Derek
AU - Lesniak, Maxine A.
AU - Böhm, Markus
AU - Maaser, Christian
AU - Kannengiesser, Klaus
AU - Donowitz, Mark
AU - Rabizadeh, Shervin
AU - Czura, Christopher J.
AU - Tracey, Kevin J.
AU - Westlake, Mark
AU - Zarfeshani, Aida
AU - Mehdi, Syed F.
AU - Danoff, Ann
AU - Ge, Xueliang
AU - Sanyal, Suparna
AU - Schwartz, Gary J.
AU - Roth, Jesse
N1 - Publisher Copyright:
© 2017 The Author(s).
PY - 2017/12/1
Y1 - 2017/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85042174457&partnerID=8YFLogxK
U2 - 10.1038/s41522-017-0039-9
DO - 10.1038/s41522-017-0039-9
M3 - Article
AN - SCOPUS:85042174457
SN - 2055-5008
VL - 3
JO - npj Biofilms and Microbiomes
JF - npj Biofilms and Microbiomes
IS - 1
M1 - 31
ER -