Interleukin-6 signaling and embryonic mouse submandibular salivary gland morphogenesis

被引:16
|
作者
Melnick, M [1 ]
Chen, HM [1 ]
Zhou, YM [1 ]
Jaskoll, T [1 ]
机构
[1] Univ So Calif, Lab Dev Genet, Los Angeles, CA 90089 USA
关键词
submandibular salivary gland; interleukin-6; tumor necrosis factor; gp130; STAT3; bcl-2; mucin; development; mouse;
D O I
10.1159/000047840
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Interleukin-6 (IL-6) is a multifunctional cytokine that mediates cell growth, differentiation, and survival. It was the objective of the present study to investigate the possible function(s) of IL-6 signaling in embryonic mouse submandibular salivary gl;and (SMG) morphogenesis. After characterizing in vivo mRNA and protein expression of various constituents of this pathway, we utilized in vitro strategies to investigate the phenotypic outcomes of enhanced IL-6-induced signaling and immunoperturbation of IL-6 binding to cognate receptors. These experiments demonstrate: (1)there is a significant increase of IL-6 mRNA with progressive SMG development, and that this is high ly correlated with TNF transcript levels; (2) IL-6 and its cognate receptors are immunolocalized in SMG branching epithelia from the canalicular stage to the late terminal bud stage, as are other constituents of the IL-6 pathway; (3) as compared to controls, IL-6-supplemented explants exhibit a substantial increase in overall size and in the number of ductal branches and terminal buds, as well as a highly significant increase in epithelial cell proliferation; (4) SMG explants cultured in the presence of anti-IL-6 neutralizing antibodies exhibit a marked decrease in epithelial ducts and terminal buds, concomitant with a significant decline in cell proliferation and a highly significant increase in apoptosis. Taken together, our experimental results indicate that IL-6 signaling is im porta nt to SMG developmental homeostasis. Copyright (C) 2001 S. Karger AG,Basel.
引用
收藏
页码:233 / 245
页数:13
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