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PLoS One. 2013 Jun 19;8(6):e64882. doi: 10.1371/journal.pone.0064882. Print 2013.

Expression of Serum Retinol Binding Protein and Transthyretin within Mouse Gastric Ghrelin Cells.

Author information

1
Departments of Internal Medicine (Divisions of Hypothalamic Research and Endocrinology & Metabolism) and Psychiatry, the University of Texas Southwestern Medical Center, Dallas, Texas, United States of America.

Abstract

Ghrelin is an orexigenic peptide hormone produced mainly by a distinct group of dispersed endocrine cells located within the gastric oxyntic mucosa. Besides secreted gene products derived from the preproghrelin gene, which include acyl-ghrelin, desacyl-ghrelin and obestatin, ghrelin cells also synthesize the secreted protein nesfatin-1. The main goal of the current study was to identify other proteins secreted from ghrelin cells. An initial gene chip screen using mRNAs derived from highly enriched pools of mouse gastric ghrelin cells demonstrated high levels of serum retinol-binding protein (RBP4) and transthyretin (TTR), both of which are known to circulate in the bloodstream bound to each other. This high expression was confirmed by quantitative RT-PCR using as template mRNA derived from the enriched gastric ghrelin cell pools and from two ghrelin-producing cell lines (SG-1 and PG-1). RBP4 protein also was shown to be secreted into the culture medium of ghrelin cell lines. Neither acute nor chronic caloric restriction had a significant effect on RBP4 mRNA levels within stomachs of C57BL/6J mice, although both manipulations significantly decreased stomach TTR mRNA levels. In vitro studies using PG-1 cells showed no effect on RBP4 release of octanoic acid, epinephrine or norepinephrine, all of which are known to act directly on ghrelin cells to stimulate ghrelin secretion. These data provide new insights into ghrelin cell physiology, and given the known functions of RBP4 and TTR, support an emerging role for the ghrelin cell in blood glucose handling and metabolism.

PMID:
23840311
PMCID:
PMC3686803
DOI:
10.1371/journal.pone.0064882
[Indexed for MEDLINE]
Free PMC Article

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