期刊
MOLECULAR AND CELLULAR ENDOCRINOLOGY
卷 522, 期 -, 页码 -出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.mce.2020.111117
关键词
Pde8b; Prkar1a; Haploinsufficiency; Tumorigenesis; beta-catenin; Steroidogenesis
资金
- Sao Paulo Research Foundation (FAPESP), Brazil [2013/05337-3]
- Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA
- Public Ministry of Labor Campinas (Research, Prevention and Education of Occupational Cancer), Brazil
The study found that PDE8B has a weak role in endocrine disorders involving the Wnt/beta-catenin signaling and PKA signaling; PDE8B appears to play a significant role in male fertility.
PDE8B, PRKAR1A and the Wnt/beta-catenin signaling are involved in endocrine disorders. However, how PDEB8B interacts with both Wnt and protein kinase A (PKA) signaling in vivo remains unknown. We created a novel Pde8b knockout mouse line (Pde8b(-/)(-)); Pde8b haploinsufficient (Pde8b(+/-)) mice were then crossed with mice harboring: (1) constitutive beta-catenin activation (Pde8b(+/)(-);Delta Cat) and (2) Prkar1a haploinsufficieny (Pde8b(+/-);Prkar1a(+/)(-)). Adrenals and testes from mice (3-12-mo) were evaluated in addition to plasma corticosterone, aldosterone and Dkk3 concentrations, and the examination of expression of steroidogenesis-, Wnt- and cAMP/PKA-related genes. Pde8b(-/-) male mice were infertile with down-regulation of the Wnt/beta-catenin pathway which did not change significantly in the Pde8b(+/-);Delta Cat mice. Prkarla haploinsufficiency also did not change the phenotype significantly. In vitro studies showed that PDE8B knockdown upregulated the Wnt pathway and increased proliferation in CTNNB1-mutant cells, whereas it downregulated the Wnt pathway in PRKAR1Amutant cells. These data support an overall weak, if any, role for PDE8B in adrenocortical tumorigenesis, even when co-altered with Wnt signaling or PKA upregulation; on the other hand, PDE8B appears to play a significant role in male fertility.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据