Instituto de Fisiología Celular, División de Neurociencias, Universidad Nacional Autónoma de México, Apartado Postal 70-253, 04510 México, DF, México.
Neurochem Res. 2011 Jan;36(1):93-102. doi: 10.1007/s11064-010-0269-1. Epub 2010 Sep 28.
Cytoskeleton proteins are substrates for proteases and further apoptotic death. We evaluated the participation of cytoskeleton in morphological changes during cell death induced by two apoptotic conditions, potassium deprivation (K5) and staurosporine, in cerebellar granule neurons (CGC). We found that K5 induced somatic damage, but neurites were relatively preserved, which corresponded to the reorganization of actin and α-tubulin in neurites. Staurosporine (STS) induced an early alteration of neurites with reorganization of cytoskeleton proteins in somas. Caspase inhibitor ZVAD totally inhibited STS-induced α-tubulin reorganization and partially blocked STS-induced actin reorganization. α-tubulin and actin reorganization induced by K5 was affected by ZVAD. Calpain inhibitor (IC1) did not affect α-tubulin or actin reorganization induced by STS, K5 or ionomycin. Neither ZVAD, nor IC1 changed α-tubulin or actin levels upon K5 treatment. STS increased α-tubulin and actin levels, but neither ZVAD nor IC1 changed α-tubulin levels upon STS treatment. In contrast, ZVAD reduced the STS-induced increase of actin. These results suggest that CGC cytoskeleton proteins undergo a differential expression and reorganization depending on the apoptotic condition.
细胞骨架蛋白是蛋白酶的底物,也是进一步细胞凋亡的底物。我们评估了细胞骨架在两种凋亡条件(低钾(K5)和星形孢菌素)诱导的小脑颗粒神经元(CGC)细胞死亡过程中形态变化中的作用。我们发现 K5 诱导体细胞损伤,但神经元突起相对保留,这与神经元突起中的肌动蛋白和α-微管蛋白的重排相对应。星形孢菌素(STS)诱导神经元突起的早期改变,同时伴有胞体中细胞骨架蛋白的重排。半胱氨酸天冬氨酸蛋白酶抑制剂 ZVAD 完全抑制 STS 诱导的α-微管蛋白重排,并部分阻断 STS 诱导的肌动蛋白重排。ZVAD 影响 K5 诱导的α-微管蛋白和肌动蛋白重排。钙蛋白酶抑制剂(IC1)不影响 STS、K5 或离子霉素诱导的α-微管蛋白或肌动蛋白重排。ZVAD 和 IC1 均未改变 K5 处理后α-微管蛋白或肌动蛋白的水平。STS 增加了α-微管蛋白和肌动蛋白的水平,但 ZVAD 和 IC1 均未改变 STS 处理后的α-微管蛋白水平。相反,ZVAD 降低了 STS 诱导的肌动蛋白增加。这些结果表明,CGC 细胞骨架蛋白根据凋亡条件经历不同的表达和重排。