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Identification of ghrelin in the house musk shrew (Suncus murinus): cDNA cloning, peptide purification and tissue distribution

Authors :
Ishida, Yuko
Sakahara, Satoshi
Tsutsui, Chihiro
Kaiya, Hiroyuki
Sakata, Ichiro
Oda, Sen-ichi
Sakai, Takafumi
Source :
Peptides. May2009, Vol. 30 Issue 5, p982-990. 9p.
Publication Year :
2009

Abstract

Abstract: Ghrelin is the endogenous ligand for the growth hormone (GH) secretagogue receptor, and the sequence of ghrelin has been determined in many species from fish to mammals. In the present study, to reveal the production of ghrelin in the house musk shrew (Suncus murinus, order: Insectivora, suncus is used as a laboratory name), we determined the cDNA sequence and structure of suncus ghrelin and also demonstrated the ghrelin-producing cells in the gastrointestinal tract. Results of cDNA cloning and mass spectrometry analysis revealed that suncus ghrelin is composed of 18 or 26 amino acid residues and that the 3rd Ser was acylated mainly by n-octanoic acid. The 10 amino acids of the N-terminal region of suncus mature ghrelin were consistent with those of other mammals. Quantitative RT-PCR revealed that suncus ghrelin mRNA is highly expressed in the gastric corpus and pyloric antrum, and low expression levels were found in various tissues, including the intestinal tract. Ghrelin cells were found only in the corpus and antrum by immunohistochemistry and in situ hybridization, and most of the ghrelin cells were closed-type cells with relatively rich cytoplasm and scattered in the glandular body and base of the gastric mucosa. The density of ghrelin cells in the corpus was significantly greater than that in the antrum. The results of this study together with our recent results regarding motilin production in the suncus indicate that the suncus will be a useful model animal for study of physiological function of the motilin/ghrelin family. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
01969781
Volume :
30
Issue :
5
Database :
Academic Search Index
Journal :
Peptides
Publication Type :
Academic Journal
Accession number :
38802449
Full Text :
https://doi.org/10.1016/j.peptides.2009.01.006