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Inhibition of Endothelial Wound Repair by Dominant Negative Connexin Inhibitors

机译:负性连接蛋白抑制剂抑制内皮伤口修复。

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Wounding of endothelial cells is associated with altered direct intercellular communication. To determine whether gap junctional communication participates to the wound repair process, we have compared connexin (Cx) expression, cell-to-cell coupling and kinetics of wound repair in monolayer cultures of PymT-transformed mouse endothelial cells (clone bEnd.3) and in bEnd.3 cells expressing different dominant negative Cx inhibitors. In parental bEnd.3 cells, mechanical wounding increased expression of Cx43 and decreased expression of Cx37 at the site of injury, whereas Cx40 expression was unaffected. These wound-induced changes in Cx expression were associated with functional changes in cell-to-cell coupling, as assessed with different fluorescent tracers. Stable transfection with cDNAs encoding for the chimeric connexin 3243H7 or the fusion protein Cx43-βGal resulted in perturbed gap junctional communication between bEnd.3 cells under both basal and wounded conditions. The time required for complete repair of a defined wound within a confluent monolayer was increased by ~50% in cells expressing the dominant negative Cx inhibitors, whereas other cell properties, such as proliferation rate, migration of single cells, cyst formation and extracellular proteolytic activity, were unaltered. These findings demonstrate that proper Cx expression is required for coordinated migration during repair of an endothelial wound.
机译:内皮细胞的受伤与直接细胞间通讯的改变有关。为了确定间隙连接通讯是否参与伤口修复过程,我们比较了连接蛋白(Cx)的表达,细胞间偶联以及PymT转化的小鼠内皮细胞(克隆bEnd.3)单层培养中伤口修复的动力学。在bEnd.3细胞中表达不同的显性负Cx抑制剂。在亲代bEnd.3细胞中,机械性损伤在受伤部位增加了Cx43的表达而降低了Cx37的表达,而Cx40的表达未受影响。这些伤口诱导的Cx表达变化与细胞间偶联的功能变化相关,如使用不同的荧光示踪剂评估的。用编码嵌合连接蛋白3243H7或融合蛋白Cx43-βGal的cDNA进行的稳定转染导致bEnd.3细胞在基础和受伤条件下均受到间隙连接通讯的干扰。在表达显性负性Cx抑制剂的细胞中,完全修复汇合的单层内确定的伤口所需的时间增加了约50%,而其他细胞特性,例如增殖率,单细胞迁移,囊肿形成和细胞外蛋白水解活性,保持不变。这些发现表明在内皮伤口修复过程中协调迁移需要正确的Cx表达。

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