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嗜铬细胞瘤PC12细胞对神经生长因子的内化作用:不存在向细胞核的转移。

Internalization of nerve growth factor by pheochromocytoma PC12 cells: absence of transfer to the nucleus.

作者信息

Rohrer H, Schäfer T, Korsching S, Thoenen H

出版信息

J Neurosci. 1982 Jun;2(6):687-97. doi: 10.1523/JNEUROSCI.02-06-00687.1982.

Abstract

The intracellular distribution of 125I-labeled nerve growth factor (NGF) in rat pheochromocytoma PC12 cells was studied by quantitative electron microscopic (EM) autoradiography and by subcellular fractionation. PC12 cells were grown as monolayer cultures in medium supplemented with serum in the presence of 125I-NGF. EM autoradiography showed that 125I-NGF was localized at the plasma membrane and cytoplasmic compartments but did not accumulate in the nuclear chromatin or in the nuclear membrane compartment of cells analyzed after 1 hr and 1, 2, and 8 d of incubation with 125I-NGF. 125I-NGF also was not detected in nuclear subcellular fractions prepared from cells grown in serum-supplemented medium either in suspension for 1 d or in monolayer cultures for 1 to 8 d. In contrast, and in confirmation of the results of Yankner and Shooter (Yankner, B. A., and E. M. Shooter (1979) Pro. Natl. Acad. Sci. U. S. A. 76: 1269-1273), about 60% of the cell-bound 125I-NGF was found in the nuclear pellet after cell fractionation if the cells had been kept previously in suspension for 1 d in phosphate-buffered saline supplemented with 0.2% glucose, 0.1% bovine serum albumin, and 125I-NGF. The ultrastructure of PC12 cells grown under such conditions, however, revealed signs of varying degrees of damage. Autoradiography of the nuclear pellet from these cells showed the grains to be located mainly over damaged nuclei or over cell debris between nuclei. It is concluded that NGF, after binding to specific receptors at the plasma membrane, is transferred to membrane-confined cytoplasmic compartments but does not have to be transferred further to the nuclear membrane or to the nuclear chromatin as a prerequisite for its physiological action.

摘要

通过定量电子显微镜放射自显影术和亚细胞分级分离法,研究了125I标记的神经生长因子(NGF)在大鼠嗜铬细胞瘤PC12细胞内的分布情况。PC12细胞在补充有血清的培养基中,于125I-NGF存在的条件下进行单层培养。电子显微镜放射自显影显示,在与125I-NGF孵育1小时以及1、2和8天后分析的细胞中,125I-NGF定位于质膜和细胞质区室,但未在核染色质或核膜区室中积累。在补充有血清的培养基中生长的细胞,无论是悬浮培养1天还是单层培养1至8天,从其制备的核亚细胞级分中也未检测到125I-NGF。相比之下,并且为了证实扬克纳和舒特(扬克纳,B.A.,以及E.M.舒特(1979年)《美国国家科学院院刊》76: 1269 - 1273)的研究结果,如果细胞先前在补充有0.2%葡萄糖、0.1%牛血清白蛋白和125I-NGF的磷酸盐缓冲盐溶液中悬浮培养1天,那么在细胞分级分离后,约60%与细胞结合的125I-NGF存在于核沉淀中。然而,在此类条件下生长的PC12细胞的超微结构显示出不同程度的损伤迹象。对这些细胞的核沉淀进行放射自显影表明,银粒主要位于受损细胞核上或细胞核之间的细胞碎片上。得出的结论是,NGF在与质膜上的特异性受体结合后,会转移至膜封闭的细胞质区室,但作为其生理作用的前提条件,并不一定需要进一步转移至核膜或核染色质。

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