Ramalingam Mahesh, Kwon Yong-Dae, Kim Sung-Jin
Department of Pharmacology and Toxicology, Metabolic Diseases Research Laboratory, Kyung Hee University, Seoul 02447, Republic of Korea.
Department of Oral and Maxillofacial Surgery, School of Dentistry, Kyung Hee University, Seoul 02447, Republic of Korea.
Biomol Ther (Seoul). 2016 Nov 1;24(6):589-594. doi: 10.4062/biomolther.2016.030.
Insulin is a peptide hormone of the endocrine pancreas and exerts a wide variety of physiological actions in insulin sensitive tissues, such as regulation of glucose homeostasis, cell growth, differentiation, learning and memory. However, the role of insulin in osteoblast cells remains to be fully characterized. In this study, we demonstrated that the insulin (100 nM) has the ability to stimulate the phosphorylation of protein kinase B (Akt/PKB) and extracellular signal-regulated kinase (ERK) and the levels of inhibin-βE in the osteoblast-like UMR-106 cells. This insulin-stimulated activities were abolished by the PI3K and MEK1 inhibitors LY294002 and PD98059, respectively. This is the first report proving that insulin is a potential candidate that enables the actions of inhibin-βE subunit of the TGF-β family. The current investigation provides a foundation for the realization of insulin as a potential stimulator in survival signaling pathways in osteoblast-like UMR-106 cells.
胰岛素是内分泌胰腺分泌的一种肽类激素,在胰岛素敏感组织中发挥多种生理作用,如调节葡萄糖稳态、细胞生长、分化、学习和记忆。然而,胰岛素在成骨细胞中的作用仍有待充分阐明。在本研究中,我们证明胰岛素(100 nM)能够刺激成骨样UMR-106细胞中蛋白激酶B(Akt/PKB)和细胞外信号调节激酶(ERK)的磷酸化以及抑制素-βE的水平。这种胰岛素刺激的活性分别被PI3K和MEK1抑制剂LY294002和PD98059所消除。这是第一份证明胰岛素是能够使转化生长因子-β家族抑制素-βE亚基发挥作用的潜在候选物的报告。目前的研究为认识胰岛素作为成骨样UMR-106细胞存活信号通路中的潜在刺激因子奠定了基础。