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动力蛋白和动力蛋白激活蛋白定位于有丝分裂上皮细胞中的星体微管和皮质位点。

Dynein and dynactin are localized to astral microtubules and at cortical sites in mitotic epithelial cells.

作者信息

Busson S, Dujardin D, Moreau A, Dompierre J, De Mey J R

机构信息

Institut Jacques Monod UMR 7592 CNRS Université Paris VII and VI 2 Place Jussieu, Tour 43, 75251, Paris, Cedex 05, France.

出版信息

Curr Biol. 1998 Apr 23;8(9):541-4. doi: 10.1016/s0960-9822(98)70208-8.

Abstract

The mitotic spindle is often positioned in a characteristic location during development, for example to enable the proper segregation of developmental determinants [1,2]. When epithelial cells divide, the mitotic spindle is often positioned parallel to the plane of the epithelium, so that both daughter cells contribute to the epithelium [3]. The mechanisms by which mitotic spindles are positioned have not been characterized in great detail, but evidence is accumulating that in some systems the dynein-dynactin microtubule motor complex plays a role [4-6]. Dynein has yet not been localized to cortical sites where it could bind to microtubules and exert a force that might orient the mitotic spindle, however [7,8]. Here, we report that in mitotic polarized epithelial cells, the dynein-dynactin complex accumulates, from prometaphase onwards, along astral microtubules and at cortical spots, into which many of the astral microtubules dock. The spots are assembled at the lateral plasma membrane, in the region below the tight junctions. Their formation is inhibited by cytochalasin D, and under these conditions the spindles do not orient properly. This novel localization of the dynein-dynactin complex is consistent with a role for the complex in the positioning of the mitotic spindle. We also show that, during prophase, the motor complex colocalizes with the nuclear envelope, consistent with it having a role in separating the centrosomes that are associated with the nuclear envelope.

摘要

在发育过程中,有丝分裂纺锤体常常定位在一个特定的位置,例如以便使发育决定因素能够正确分离[1,2]。上皮细胞分裂时,有丝分裂纺锤体常常与上皮平面平行定位,这样两个子细胞都能为上皮层做出贡献[3]。有丝分裂纺锤体定位的机制尚未得到详细描述,但越来越多的证据表明,在某些系统中动力蛋白 - 动力蛋白激活蛋白微管运动复合体发挥了作用[4 - 6]。然而,动力蛋白尚未定位于皮质位点,在那里它可以与微管结合并施加可能使有丝分裂纺锤体定向的力[7,8]。在此,我们报告在有丝分裂的极化上皮细胞中,从前期开始,动力蛋白 - 动力蛋白激活蛋白复合体沿着星体微管并在皮质斑点处积累,许多星体微管对接于这些皮质斑点。这些斑点在紧密连接下方区域的外侧质膜处组装。它们的形成受到细胞松弛素D的抑制,在这些条件下纺锤体不能正确定向。动力蛋白 - 动力蛋白激活蛋白复合体的这种新定位与该复合体在有丝分裂纺锤体定位中的作用一致。我们还表明,在前期,运动复合体与核膜共定位,这与其在分离与核膜相关的中心体中发挥作用一致。

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