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完整角膜上皮组织中肌动蛋白与α-辅肌动蛋白之间的细胞内关系。

Intracellular relationship between actin and alpha-actinin in a whole corneal epithelial tissue.

作者信息

Khoory W, Wu E, Svoboda K K

机构信息

Department of Anatomy and Neurobiology, Boston University School of Medicine, MA 02118.

出版信息

J Cell Sci. 1993 Nov;106 ( Pt 3):703-17. doi: 10.1242/jcs.106.3.703.

Abstract

Alpha-actinin is an actin crosslinking protein that may be one of the proteins involved in the attachment of the actin cytoskeletal framework to the plasma membrane. We investigated the distribution of alpha-actinin in whole-mount embryonic chick corneal epithelia using confocal laser scanning analysis. The intracellular alpha-actinin distribution was compared with F-actin using phalloidin, or total actin using an anti-actin antibody. Corneal epithelial tissues were isolated with or without the basal lamina (+ or -BL), and fixed immediately. In addition, epithelia isolated -BL were cultured for 2 hours with either control medium, laminin-supplemented medium or laminin and cytochalasin D (CD)-containing medium. The single- and double-labeled epithelia showed that alpha-actinin delineated the cell borders and microvilli of the periderm cells in the most apical optical sections of control and laminin-treated epithelia. At the optical plane through the basal cell nuclei, the alpha-actinin was distributed diffusely throughout the cytoplasm, whereas the actin was sparse, only associated with the lateral cell membranes. Epithelia (-BL) cultured in control medium had cytoplasmic protrusions or blebs on the basal cell surface. The blebs contained both actin and alpha-actinin. In epithelial cultured with laminin, the basal cell surface was flat. The actin cortical mat became reorganized within two hours. Actin and alpha-actinin were colocalized in the re-formed basal cytoskeletal network. In cells cultured with cytochalasin D (CD) and laminin the actin cortical mat was not reorganized. Actin networks from both cell layers were eliminated and replaced by aggregates scattered throughout the cytoplasm. The alpha-actinin remained diffusely distributed in the cytoplasm and failed to colocalize with the actin aggregates. The alpha-actinin appeared closer to the basal cell membrane than the actin in cross-sectional views of the tissue. Results from these double-labeling experiments confirmed the intimate association of alpha-actinin and actin in the laminin-stimulated actin cortical mat reorganization. This study is the first to demonstrate that CD-aggregated F-actin does not capture the alpha-actinin. The alpha-actinin appeared to remain diffuse throughout the cytoplasm and separate from F-actinin; however, there was some overlap with G-actin.

摘要

α-辅肌动蛋白是一种肌动蛋白交联蛋白,可能是参与肌动蛋白细胞骨架框架与质膜附着的蛋白之一。我们使用共聚焦激光扫描分析研究了α-辅肌动蛋白在鸡胚角膜上皮全层中的分布。将细胞内α-辅肌动蛋白的分布与使用鬼笔环肽的F-肌动蛋白或使用抗肌动蛋白抗体的总肌动蛋白进行了比较。分离有或无基底层(+或 -BL)的角膜上皮组织,并立即固定。此外,将分离的 -BL上皮细胞在对照培养基、添加层粘连蛋白的培养基或含有层粘连蛋白和细胞松弛素D(CD)的培养基中培养2小时。单标记和双标记上皮细胞显示,在对照和层粘连蛋白处理的上皮细胞最顶端光学切片中,α-辅肌动蛋白勾勒出周皮细胞的细胞边界和微绒毛。在穿过基底细胞核的光学平面上,α-辅肌动蛋白弥漫分布于整个细胞质中,而肌动蛋白稀疏,仅与细胞侧面细胞膜相关。在对照培养基中培养的上皮细胞(-BL)在基底细胞表面有细胞质突起或泡状结构。这些泡状结构同时含有肌动蛋白和α-辅肌动蛋白。在用层粘连蛋白培养的上皮细胞中,基底细胞表面是平的。肌动蛋白皮质垫在两小时内重新组织。肌动蛋白和α-辅肌动蛋白共定位于重新形成的基底细胞骨架网络中。在用细胞松弛素D(CD)和层粘连蛋白培养的细胞中,肌动蛋白皮质垫未重新组织。来自两个细胞层的肌动蛋白网络被消除,取而代之的是散布在整个细胞质中的聚集体。α-辅肌动蛋白仍弥漫分布于细胞质中,未能与肌动蛋白聚集体共定位。在组织的横截面视图中,α-辅肌动蛋白比肌动蛋白更靠近基底细胞膜。这些双标记实验的结果证实了α-辅肌动蛋白与肌动蛋白在层粘连蛋白刺激的肌动蛋白皮质垫重组中的密切关联。本研究首次证明CD聚集的F-肌动蛋白不会捕获α-辅肌动蛋白。α-辅肌动蛋白似乎在整个细胞质中保持弥散状态,并与F-肌动蛋白分离;然而,与G-肌动蛋白有一些重叠。

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