Sweet S C, Rogers C M, Welsh M J
Department of Anatomy and Cell Biology, University of Michigan Medical School, Ann Arbor 48109-0616.
J Cell Biol. 1988 Dec;107(6 Pt 1):2243-51. doi: 10.1083/jcb.107.6.2243.
To investigate the function of calmodulin (CaM) in the mitotic apparatus, the effect of microinjected CaM and chemically modified CaMs on nocodazole-induced depolymerization of spindle microtubules was examined. When metaphase PtK1 cells were microinjected with CaM or a CaM-TRITC conjugate, kinetochore microtubules (kMTs) were protected from the effect of nocodazole. The ability of microinjected CaM to subsequently protect kMTs from the depolymerizing effect of nocodazole was dose dependent, and was effective for approximately 45 min, with protection decreasing if nocodazole treatment was delayed for more than 60 min after injection of CaM. The CaM-TRITC conjugate, similar to native CaM, displayed the ability to activate bovine brain CaM-dependent adenylate cyclase in a Ca++-dependent manner and showed a Ca++-dependent mobility shift when subjected to PAGE. A heat-altered CaM-TRITC conjugate also protected kMTs from the effect of nocodazole. However, this modified CaM was not able to activate adenylate cyclase nor did it display a Ca++-dependent mobility shift when electrophoresed. In a permeabilized cell model system, both CaM analogs were observed to bind to the spindle in a Ca++-independent manner. In contrast, a performic acid-oxidized CaM did not have a protective effect on spindle structure when microinjected into metaphase cells before nocodazole treatment. The oxidized CaM did not activate adenylate cyclase and did not exhibit Ca++-dependent mobility on polyacrylamide gels. These results are interpreted as supporting the hypothesis that CaM binds to the mitotic spindle in a Ca++-independent manner and that CaM may serve in the spindle, at least in part, to stabilize kMTs.
为了研究钙调蛋白(CaM)在有丝分裂器中的功能,研究了显微注射CaM和化学修饰的CaM对诺考达唑诱导的纺锤体微管解聚的影响。当向中期PtK1细胞显微注射CaM或CaM-TRITC偶联物时,动粒微管(kMTs)受到保护,免受诺考达唑的影响。显微注射的CaM随后保护kMTs免受诺考达唑解聚作用的能力呈剂量依赖性,并且在约45分钟内有效,如果在注射CaM后延迟60分钟以上进行诺考达唑处理,保护作用会降低。CaM-TRITC偶联物与天然CaM相似,能够以Ca++依赖的方式激活牛脑CaM依赖性腺苷酸环化酶,并且在进行聚丙烯酰胺凝胶电泳(PAGE)时显示出Ca++依赖的迁移率变化。热改变的CaM-TRITC偶联物也能保护kMTs免受诺考达唑的影响。然而,这种修饰的CaM不能激活腺苷酸环化酶,在电泳时也不显示Ca++依赖的迁移率变化。在透化细胞模型系统中,观察到两种CaM类似物均以Ca++不依赖的方式与纺锤体结合。相比之下,过甲酸氧化的CaM在诺考达唑处理前显微注射到中期细胞中时,对纺锤体结构没有保护作用。氧化的CaM不能激活腺苷酸环化酶,在聚丙烯酰胺凝胶上也不表现出Ca++依赖的迁移率。这些结果被解释为支持以下假设:CaM以Ca++不依赖的方式与有丝分裂纺锤体结合,并且CaM可能至少部分地在纺锤体中起到稳定kMTs的作用。