Clermont Y, Rambourg A, Hermo L
Department of Anatomy and Cell Biology, McGill University, Montreal, Canada.
Anat Rec. 1994 Dec;240(4):469-80. doi: 10.1002/ar.1092400405.
The exact structural relationships of the saccules, membranous tubules, and vesicles that compose the cis- and mid-compartments of the Golgi cortex of rat spermatids was investigated to determine the relationship of these elements to each other.
Tissues fixed with glutaraldehyde and buffered in sodium cacodylate were examined with the electron microscope. Electron micrographs, including stereopairs, were analyzed to determine the three-dimensional organization of the Golgi elements.
The deeper layer of the Golgi cortex was composed of stacks of saccules connected to each other either by saccules or membranous tubules. The peripheral region of the Golgi cortex, located between the cis-side of the stacks and a network of overlying ER cisternae contained numerous membranous tubules and vesicles of two class sizes: 50-100 nm vesicles and microvesicles 5-10 nm in diameter. The tubules formed tight networks, known as cis-elements or cis-Golgi networks (CGN), which were strictly parallel and next to the first or cis-saccule of the stack. The cis-elements were continuous with more loosely arranged peripheral tubules which formed elaborate, intertwined and interconnected networks. These peripheral tubules closely approximated the overlying ER cisternae in areas often showing fuzz-coated finger-like projections. Occasionally such peripheral tubules were continuous with ER cisternae. The saccules forming the stacks were continuous with membranous tubules which not only connected saccules of adjacent stacks, but also saccules of the same stack. These tubules were also connected with the tight tubular networks forming the cis-elements and the broad networks formed by the peripheral membranous tubules. Vesicles (50-100 nm) and microvesicles (5-10 nm) frequently formed aggregates in the peripheral Golgi region next to areas of ER membrane free of fuzz-coated projections. The microvesicles, embedded in a denser cytoplasmic matrix, had a more or less distinct delimiting membrane suggestive of their disintegration in this juxta-ER location. The 50-100 nm vesicles that were seen at the periphery of the vesicular aggregates appeared to form mainly from the membranous tubules of the Golgi cortex.
Thus the saccules and membranous tubules of the spermatid's Golgi cortex formed a single continuous membraneous system connected to ER cisternae. The vesicles, seemingly arising from the membranous tubules, appear to follow a retrograde pathway and undergo dissolution next to ER cisternae.
研究了构成大鼠精子细胞高尔基皮质顺式和中间区室的囊泡、膜性小管和小泡的确切结构关系,以确定这些成分之间的相互关系。
用戊二醛固定并用二甲胂酸钠缓冲的组织用电子显微镜检查。分析电子显微照片,包括立体对,以确定高尔基成分的三维组织。
高尔基皮质的深层由通过囊泡或膜性小管相互连接的囊泡堆叠组成。高尔基皮质的周边区域位于堆叠的顺式侧和覆盖的内质网池网络之间,包含许多膜性小管和两种大小的小泡:50-100nm的小泡和直径5-10nm的微泡。这些小管形成紧密的网络,称为顺式元件或顺式高尔基网络(CGN),它们严格平行且紧邻堆叠的第一个或顺式囊泡。顺式元件与排列更松散的周边小管连续,这些周边小管形成复杂的、相互交织和相互连接的网络。这些周边小管在经常显示有绒毛覆盖的指状突起的区域紧密靠近覆盖的内质网池。偶尔,这样的周边小管与内质网池连续。形成堆叠的囊泡与膜性小管连续,这些膜性小管不仅连接相邻堆叠的囊泡,也连接同一堆叠的囊泡。这些小管还与形成顺式元件的紧密管状网络以及由周边膜性小管形成的广泛网络相连。囊泡(50-100nm)和微泡(5-10nm)经常在高尔基周边区域靠近没有绒毛覆盖突起的内质网膜区域形成聚集体。微泡嵌入较致密的细胞质基质中,有或多或少明显的界定膜,表明它们在这个紧邻内质网的位置发生解体。在囊泡聚集体周边看到的50-100nm囊泡似乎主要由高尔基皮质的膜性小管形成。
因此,精子细胞高尔基皮质的囊泡和膜性小管形成了一个与内质网池相连的单一连续膜系统。这些囊泡似乎起源于膜性小管,似乎遵循逆行途径并在内质网池附近发生溶解。