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Merck
  • Defective autophagy in vascular smooth muscle cells accelerates senescence and promotes neointima formation and atherogenesis.

Defective autophagy in vascular smooth muscle cells accelerates senescence and promotes neointima formation and atherogenesis.

Autophagy (2015-09-24)
Mandy Oj Grootaert, Paula A da Costa Martins, Nicole Bitsch, Isabel Pintelon, Guido Ry De Meyer, Wim Martinet, Dorien M Schrijvers
摘要

Autophagy is triggered in vascular smooth muscle cells (VSMCs) of diseased arterial vessels. However, the role of VSMC autophagy in cardiovascular disease is poorly understood. Therefore, we investigated the effect of defective autophagy on VSMC survival and phenotype and its significance in the development of postinjury neointima formation and atherosclerosis. Tissue-specific deletion of the essential autophagy gene Atg7 in murine VSMCs (atg7

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单克隆抗 β-肌动蛋白抗体 小鼠抗, clone AC-15, ascites fluid
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单克隆抗-肌动蛋白,α-平滑肌, clone 1A4, ascites fluid
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衰老细胞组织化学染色试剂盒, sufficient for 100 tests
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抗-肌动蛋白,α-平滑肌- FITC抗体,小鼠单克隆 小鼠抗, clone 1A4, purified from hybridoma cell culture
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抗p62/SQSTM1 兔抗, ~1 mg/mL, affinity isolated antibody, buffered aqueous solution
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抗-ATG7 兔抗, affinity isolated antibody, buffered aqueous solution
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抗-ATG5(N-末端) 兔抗, affinity isolated antibody, PBS solution
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抗-p53 (乙酰赖氨酸317),C末端 兔抗, affinity isolated antibody