Snyder J A
Department of Biological Sciences, University of Denver, CO 80208.
Cell Motil Cytoskeleton. 1988;11(4):291-302. doi: 10.1002/cm.970110407.
Hyperosmotic sucrose treatment of metaphase PtK-1 cells has been shown to produce a reversible concentration-dependent effect on spindle elongation linked to a functional alteration in the connection of the chromosome to the spindle (Pover et al.: European Journal of Cell Biology 39:366-372, 1985). Spindle elongation, similar to that which occurs at anaphase B, is thought to be driven by the compression stored in the form of microtubule curvature in the nonkinetochore (nkMT) population of microtubules at metaphase (Snyder et al.: European Journal of Cell Biology 35:62-69, 1984 and 39:373-379, 1985). Addition of metabolic inhibitors to Ham's F-12 salts with deoxyglucose (D/F-12 medium) containing 0.4 M sucrose and 1 mM DNP does not within statistical error affect the rate and extent of sucrose-induced spindle elongation; rates and extents are 60-75% of normal anaphase B motions. Electron microscopic analysis of metaphase cells treated with D/F-12 medium and 0.4 M sucrose with 1 mM DNP demonstrates that spindle microtubules lose curvature and become straight in appearance, typical of microtubule organization in untreated anaphase cells. Sucrose-treated cells released into D/F-12 medium show a rapid reduction in spindle length; however, cells treated with either 0.4 M sucrose or 0.4 M sucrose and 1 mM DNP-containing D/F-12 medium and released into DNP-containing D/F-12 medium do not exhibit a significant reduction in spindle length. Electron microscopic analysis links changes in spindle length with microtubule/kinetochore associations. These data suggest that energy required for the initial phases of spindle elongation during anaphase is preloaded into the mitotic spindle by metaphase and does not require additional energy to be expressed as examined by sucrose-induced spindle elongation in the presence of metabolic inhibitors. Second, energy is required to make or maintain (or both) functional chromosome associations with the spindle as measured by reduction in spindle length following sucrose removal.
已证明,用高渗蔗糖处理中期PtK - 1细胞会对纺锤体伸长产生可逆的浓度依赖性影响,这种影响与染色体与纺锤体连接的功能改变有关(波弗等人:《欧洲细胞生物学杂志》39:366 - 372,1985年)。纺锤体伸长类似于后期B发生的情况,被认为是由中期非动粒(nkMT)微管群体中以微管曲率形式储存的压缩力驱动的(斯奈德等人:《欧洲细胞生物学杂志》35:62 - 69,1984年和39:373 - 379,1985年)。向含有0.4 M蔗糖和1 mM二硝基苯酚(DNP)的含脱氧葡萄糖的哈姆F - 12盐溶液(D/F - 12培养基)中添加代谢抑制剂,在统计误差范围内不会影响蔗糖诱导的纺锤体伸长的速率和程度;速率和程度为正常后期B运动的60 - 75%。对用含1 mM DNP的D/F - 12培养基和0.4 M蔗糖处理的中期细胞进行电子显微镜分析表明,纺锤体微管失去曲率,外观变直,这是未处理后期细胞中微管组织的典型特征。释放到D/F - 12培养基中的蔗糖处理细胞纺锤体长度迅速缩短;然而,用0.4 M蔗糖或含0.4 M蔗糖和1 mM DNP的D/F - 12培养基处理并释放到含DNP的D/F - 12培养基中的细胞纺锤体长度没有显著缩短。电子显微镜分析将纺锤体长度的变化与微管/动粒关联联系起来。这些数据表明,后期纺锤体伸长初始阶段所需的能量在中期就预先加载到有丝分裂纺锤体中,并且在存在代谢抑制剂的情况下,通过蔗糖诱导的纺锤体伸长检测,不需要额外能量来表达。其次,如去除蔗糖后纺锤体长度缩短所测量的那样,建立或维持(或两者)染色体与纺锤体的功能关联需要能量。