Author:
Dalm Virgil A. S. H.,van Hagen P. Martin,van Koetsveld Peter M.,Achilefu Sam,Houtsmuller Adriaan B.,Pols David H. J.,van der Lely Aart-Jan,Lamberts Steven W. J.,Hofland Leo J.
Abstract
Increasing evidence suggests that neuropeptides play a role in the regulatory mechanisms between the neuroendocrine and immune systems. A differential expression of the five known somatostatin (SS) receptors (sst1–5) has been demonstrated in human immune cells and tissues. However, little is known concerning regulation and expression of sst1–5and the peptide SS. Therefore, we investigated the expression and the time-dependent regulation of sst1–5, SS, and cortistatin (CST), a novel SS-like peptide, in human monocytes (MO), monocyte-derived macrophages (MP), and dendritic cells (DC) in the basal and lipopolysaccharide (LPS)-activated state. MO, MP, and DC selectively expressed sst2mRNA. SS mRNA was not detectable, whereas all samples expressed CST mRNA. Expression levels of sst2and CST mRNA showed marked differences and were in the rank order of MP>>DC>>>MO. LPS stimulation did not induce expression of SS or sst1,3,4,5. However, sst2mRNA expression was upregulated significantly by stimulation with LPS. CST mRNA was upregulated as well. During differentiation of MO in MP or DC, time-dependent, significantly increasing sst2and CST mRNA levels were found. By confocal microscopy, the presence of sst2receptors was demonstrated on MP, but not on DC. This study demonstrates for the first time a selective and inducible expression of the recently discovered CST, as well as sst2, in human monocyte-derived cells, suggesting a role for a CST-sst2system rather than a SS-sst2system in these immune cell types.
Publisher
American Physiological Society
Subject
Physiology (medical),Physiology,Endocrinology, Diabetes and Metabolism
Cited by
154 articles.
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