Louvard D, Reggio H, Warren G
J Cell Biol. 1982 Jan;92(1):92-107. doi: 10.1083/jcb.92.1.92.
Rabbits were immunized with membrane fractions from either the Golgi complex or the rough endoplasmic reticulum (RER) by injection into the popliteal lymph nodes. The antisera were then tested by indirect immunofluorescence on tissue culture cells or frozen, thin sections of tissue. There were may unwanted antibodies to cell components other than the RER or the Golgi complex, and these were removed by suitable absorption steps. These steps were carried out until the pattern of fluorescent labeling was that expected for the Golgi complex or RER. Electron microscopic studies, using immunoperoxidase labeling of normal rat kidney (NRK) cells, showed that the anti-Golgi antibodies labeled the stacks of flattened cisternae that comprise the central feature of the Golgi complex, many of the smooth vesicles around the stacks, and a few coated vesicles. These antibodies were directed, almost entirely, against a single polypeptide with an apparent molecular weight of 135,000. The endoplasmic reticulum (ER) in NRK cells is an extensive, reticular network that pervades the entire cell cytoplasm and includes the nuclear membrane. The anit-RER antibodies labeled this structure alone at the light and electron microscopic levels. They were largely directed against four polypeptides with apparent molecular weights of 29,000, 58,000, 66,000, and 91,000. Some examples are presented, using immunofluorescence microscopy, where these antibodies have been used to study the Golgi complex and RER under a variety of physiological and experimental condition . For biochemical studies, these antibodies should prove useful in identifying the origin of isolated membranes, particularly those from organelles such as the Golgi complex, which tend to lose their characteristic morphology during isolation.
通过将来自高尔基体复合体或粗面内质网(RER)的膜组分注射到腘淋巴结中,对兔子进行免疫。然后通过间接免疫荧光法在组织培养细胞或冷冻的组织薄片上检测抗血清。除了RER或高尔基体复合体之外,还有许多针对细胞成分的不需要的抗体,这些抗体通过适当的吸收步骤被去除。这些步骤一直进行到荧光标记模式符合高尔基体复合体或RER的预期模式。使用免疫过氧化物酶标记正常大鼠肾(NRK)细胞的电子显微镜研究表明,抗高尔基体抗体标记了构成高尔基体复合体主要特征的扁平囊泡堆叠、堆叠周围的许多光滑小泡以及一些有被小泡。这些抗体几乎完全针对一种表观分子量为135,000的单一多肽。NRK细胞中的内质网(ER)是一个广泛的网状网络,遍布整个细胞质,包括核膜。抗RER抗体在光镜和电镜水平上仅标记了这种结构。它们主要针对四种表观分子量分别为29,000、58,000、66,000和91,000的多肽。本文给出了一些使用免疫荧光显微镜的例子,其中这些抗体已被用于在各种生理和实验条件下研究高尔基体复合体和RER。对于生化研究,这些抗体在鉴定分离膜的来源方面应该是有用的,特别是那些来自高尔基体复合体等细胞器的膜,这些细胞器在分离过程中往往会失去其特征形态。