Affiliation:
1. Departments of Dermatology and Biological Chemistry, University of California, Irvine, California
Abstract
SLURP-1 (secreted mammalian Ly-6/urokinase plasminogen activator receptor-related protein-1) is a novel auto/paracrine cholinergic peptide that can bind to α7-nicotinic acetylcholine receptor (nAChR), a high Ca2+-permeable ion channel coupled to regulation of nuclear factor-κB (NF-κB) expression. Elucidation of intracellular signaling events elicited by SLURP-1 is crucial for understanding the molecular mechanism of functioning of this novel hormone-like peptide that alters vital cell functions and can protect from tumorigenic transformation. In this study, we sought to dissect out the role of α7-nAChR in mediating the biologic effects of recombinant SLURP-1 on the immortalized line of human oral keratinocytes Het-1A. A multifold upregulation of the NF-κB expression at the mRNA and protein levels by SLURP-1 was only slightly diminished due to elimination of Na+, whereas in Ca2+-free medium the effect of SLURP-1 was inhibited by >50%. Both in the absence of extracellular Ca2+ and in the presence of Cd2+ or Zn2+, the SLURP-1-dependent elevation of NF-κB was almost completely blocked by inhibiting MEK1 activity. Downstream of α7-nAChR, the SLURP-1 signaling coupled to upregulation of NF-κB also involved Jak2 as well as Ca2+/calmodulin-dependent kinase II (CaMKII) and protein kinase C (PKC), whose inhibition significantly ( P < 0.05) reduced the SLURP-1-induced upregulation of NF-κB. The obtained results indicated that activation of α7-nAChR by SLURP-1 leads to upregulation of the NF-κB gene expression due to activation of the Raf-1/MEK1/ERK1/2 cascade that proceeds via two complementary signaling pathways. One is mediated by the Ca2+-entry dependent CaMKII/PKC activation and another one by Ca2+-independent involvement of Jak2. Thus, there exists a previously not appreciated network of noncanonical auto/paracrine ligands of nAChR of the Ly-6 protein family, which merits further investigations.
Publisher
American Physiological Society
Cited by
55 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献