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This Article Accepted manuscript (PDF) All Versions of this Article: JOE-09-0086v1 202/3/355    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Wang, X. Articles by Hu, R. Search for Related Content PubMed PubMed Citation Articles by Wang, X. Articles by Hu, R.

X Wang, Department of Endocrinology, Huashan Hospital, Shanghai, 200040, China
W Gong, Shanghai, China
Y Liu, Shanghai, China
Z Yang, Shanghai, China
W Zhou, Shanghai, China
M Wang, Shanghai, China
Z Yang, Shanghai, China
J Wen, Shanghai, China
R Hu, Shanghai, China

Correspondence: Xuanchun Wang, Email: wangxch{at}fudan.edu.cn

We report the identification of a novel secreted peptide, INM02. The mRNA transcript of human INM02 gene is about 3.0 kilo basepairs. Its ORF contains 762 basepairs and encodes a protein of 254 amino acids. Northern blot analysis demonstrates that INM02 mRNA is widely expressed in rat tissues, especially with abundant quantities in pancreatic islets, testis, and bladder tissue. We have expressed recombinant INM02 protein and generated rabbit anti-INM02 polyclonal antibodies. INM02 could be detectable in human serum by ELISA we established. We also present evidence that INM02 mRNA expression could be regulated by glucose. Experiments on both MIN6 cells and intact isolated islets demonstrate that INM02 mRNA levels are increased more than 3-fold by high glucose (25 mM) when compared with low glucose (5.5 mM). ELISA analysis shows that secretion of INM02 is significantly augmented by high glucose in vitro. It is speculated that as a novel secreted protein, INM02 is associated with functions of pancreatic islets, especially of β cells.