Brown D, Lee R, Bonventre J V
Renal Unit, Massachusetts General Hospital, Boston, USA.
Am J Physiol. 1997 Dec;273(6):F1003-12. doi: 10.1152/ajprenal.1997.273.6.F1003.
After ischemia and reperfusion, severe alterations in the cytoskeletal organization of renal tubular epithelial cells have been reported. These effects, accompanied by a modification in the polarized distribution of some membrane transport proteins, are especially evident in the proximal tubule. In normal proximal tubule cells, actin is concentrated in apical brush border microvilli, along with the actin-binding protein villin. Because villin plays an important role in actin bundling and in microvillar assembly but can also act as an actin-fragmenting protein at higher calcium concentrations, we examined the effects of ischemic injury and reperfusion on the distribution of villin and actin in proximal tubule cells of rat kidney. Using specific antibodies against villin and actin, we show that these proteins redistribute in parallel from the apical to the basolateral plasma membrane within 1 h of reperfusion after ischemia. Ischemia alone had no effect on the staining pattern. Repolarization of villin to the apical membrane begins within hours after reperfusion with enhanced apical localization over time during the period of regeneration. This apical repolarization of villin is accompanied by the migration of actin back to the apical membrane. These results show not only that villin may be involved in the initial disruption of the actin cytoskeleton during reperfusion injury but also that its migration back to the apical domain of these cells accompanies the reestablishment of a normal actin distribution in the brush border.
据报道,缺血再灌注后,肾小管上皮细胞的细胞骨架组织会发生严重改变。这些效应伴随着一些膜转运蛋白极化分布的改变,在近端小管中尤为明显。在正常的近端小管细胞中,肌动蛋白与肌动蛋白结合蛋白绒毛蛋白一起集中在顶端刷状缘微绒毛中。由于绒毛蛋白在肌动蛋白成束和微绒毛组装中起重要作用,但在较高钙浓度下也可作为肌动蛋白切割蛋白,我们研究了缺血损伤和再灌注对大鼠肾脏近端小管细胞中绒毛蛋白和肌动蛋白分布的影响。使用针对绒毛蛋白和肌动蛋白的特异性抗体,我们发现这些蛋白质在缺血后再灌注1小时内从顶端质膜平行重新分布到基底外侧质膜。单独缺血对染色模式没有影响。绒毛蛋白重新极化到顶端膜在再灌注后数小时内开始,并在再生期间随着时间的推移顶端定位增强。绒毛蛋白的这种顶端重新极化伴随着肌动蛋白向顶端膜的迁移。这些结果不仅表明绒毛蛋白可能参与再灌注损伤期间肌动蛋白细胞骨架的初始破坏,而且还表明其迁移回这些细胞的顶端区域伴随着刷状缘中正常肌动蛋白分布的重新建立。