| Literature DB >> 24184700 |
Li Wang1, Lichun Liu1, Yang Zhou1, Xiaoheng Zhao1, Mingjun Xi1, Shun Wei1, Rui Fang1, Wei Ji1, Nan Chen1, Zemao Gu1, Xueqin Liu1, Weimin Wang2, Muhammad Asim1, Xiaoling Liu3, Li Lin4.
Abstract
Mannose receptor C type 1 (MRC1) is a pattern-recognition receptor (PRR) which plays a significant role in immune responses. Much work on MRC1 has been done in mammals and birds while little in fish. In this study, we cloned and characterized MRC1 in grass carp (gcMR). The full-length gcMR contained 5291bp encoding a putative protein of 1432 amino acids. The predicted amino acid sequences showed that gcMR contained a signal peptide, a cysteine-rich (CR) domain, a fibronectin type II (FN II) domain, eight C-type lectin-like domains (CTLDs), a transmembrane domain and a short cytoplasmic domain. gcMR were constitutively expressed in different organs with the higher expression in spleen and head kidney. During embryonic development, gcMR transcript levels were highest at cleavage stage. The up-regulation expression of gcMR, IL-1β and TNF-α in liver, spleen, head kidney and intestine after Aeromonas hydrophila infection indicating it involved in innate immune regulation during bacterial infections. CrownEntities:
Keywords: Aeromonas hydrophila; Expression; Grass carp (Ctenopharyngodon idella); Mannose receptor C type 1 (MRC1)
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Year: 2013 PMID: 24184700 DOI: 10.1016/j.dci.2013.10.006
Source DB: PubMed Journal: Dev Comp Immunol ISSN: 0145-305X Impact factor: 3.636