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Induction of cysteine-rich motor neuron 1 mRNA expression in vascular endothelial cells
Authors:Yukiko Nakashima  Satoru Takahashi
Affiliation:1. Department of Immunobiology, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women’s University, 11-68 Kohshien Kyuban-cho, Nishinomiya, Hyogo 663-8179, Japan;2. First Department of Biochemistry, School of Pharmaceutical Sciences, Kyushu University of Health and Welfare, 1714-1 Yoshino, Nobeoka, Miyazaki 882-0072, Japan;3. Institute for Biosciences, Mukogawa Women’s University, 11-68 Kohshien Kyuban-cho, Nishinomiya, Hyogo 663-8179, Japan
Abstract:Cysteine-rich motor neuron 1 (CRIM1) is expressed in vascular endothelial cells and plays a crucial role in angiogenesis. In this study, we investigated the expression of CRIM1 mRNA in human umbilical vein endothelial cells (HUVECs). CRIM1 mRNA levels were not altered in vascular endothelial growth factor (VEGF)-stimulated monolayer HUVECs or in cells in collagen gels without VEGF. In contrast, the expression of CRIM1 mRNA was elevated in VEGF-stimulated cells in collagen gels. The increase in CRIM1 mRNA expression was observed even at 2 h when HUVECs did not form tubular structures in collagen gels. Extracellular signal-regulated kinase (Erk) 1/2, Akt and focal adhesion kinase (FAK) were activated by VEGF in HUVECs. The VEGF-induced expression of CRIM1 mRNA was significantly abrogated by PD98059 or PF562271, but was not affected by LY294002. These results demonstrate that CRIM1 is an early response gene in the presence of both angiogenic stimulation (VEGF) and environmental (extracellular matrix) factors, and Erk and FAK might be involved in the upregulation of CRIM1 mRNA expression in vascular endothelial cells.
Keywords:CRIM1, cysteine-rich motor neuron 1   HUVEC, human umbilical vein endothelial cell   VEGF, vascular endothelial growth factor   bFGF, basic fibroblast growth factor   Erk, extracellular signal-regulated kinase   FAK, focal adhesion kinase   GAPDH, glyceraldehyde-3-phosphate dehydrogenase
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