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一种用于体外培养人类细胞的显微外科方法:演变与应用

A microsurgical methodology for human cells in vitro: evolution and applications.

作者信息

Diacumakos E G, Holland S, Pecora P

出版信息

Proc Natl Acad Sci U S A. 1970 Apr;65(4):911-8. doi: 10.1073/pnas.65.4.911.

Abstract

A methodology for micromanipulating human cells of normal and malignant origin, in vitro, has evolved from the study of about 2000 HeLa, ERK (a subline of HeLa cells), and human embryonic lung cells during interphase and mitosis. It is now possible to microinject interphase cells with aqueous and nonaqueous fluids intracytoplasmically. Chromosomes from human embryonic lung metaphase cells have been transplanted. Chromosomes have been manipulated within mitotic human embryonic lung, ERK, and HeLa cells. Clones have been obtained from HeLa cells subjected to such manipulation. Predictable derangements of mitotic cells and their progeny have been obtained. Intranuclear injections of silicone oil, DNA, and sodium chloride solutions have been made with survival of the cells. HeLa cells have been cloned from such injected cells. Subcellular fractions have been introduced into the nuclei and cytoplasms of HeLa and human embryonic lung cells. The lung cells have been subjected to nuclear micropuncture in groups and a clone has been obtained. Virus suspensions have been introduced into the nuclei of HeLa cells without killing the cells. Applications of this methodology are discussed.

摘要

一种用于在体外对正常和恶性来源的人类细胞进行显微操作的方法,是在对约2000个海拉细胞、ERK(海拉细胞的一个亚系)和人胚肺细胞在间期和有丝分裂期的研究过程中发展而来的。现在已能够将水性和非水性液体胞质内显微注射到间期细胞中。人胚肺中期细胞的染色体已被移植。染色体已在有丝分裂期的人胚肺细胞、ERK细胞和海拉细胞内进行了操作。已从经过此类操作的海拉细胞中获得了克隆。已获得有丝分裂细胞及其后代的可预测紊乱情况。已对细胞核进行硅油、DNA和氯化钠溶液的注射,且细胞存活。已从此类注射细胞中克隆出海拉细胞。已将亚细胞组分引入海拉细胞和人胚肺细胞的细胞核及细胞质中。已对成组的肺细胞进行细胞核微穿刺并获得了一个克隆。已将病毒悬液引入海拉细胞的细胞核而未杀死细胞。讨论了该方法的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/948e/283003/6fb3dcb51507/pnas00095-0144-a.jpg

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