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植入前小鼠胚胎中细胞质磷酸酶的超微结构定位

Ultrastructural localization of cytoplasmic phosphatases in preimplantation mouse embryos.

作者信息

Vorbrodt A, Konwiński M, Solter D, Koprowski H

出版信息

Folia Histochem Cytochem (Krakow). 1976;14(4):249-56.

PMID:192644
Abstract

The appearance and localization of the cytoplasmic phosphatases [acid phosphatase (AcPase) as a marker of lysosomes, TPPase as a marker of the Golgi apparatus, and NDPase (IDPase) as enzymatic marker of the endoplasmic reticulum (ER)] were cytochemically studied on the ultrastructural level in secondary oocytes and in preimplantation mouse embryos. The detectable AcPase activity, located on the inner surface of the membrane delimiting some cytoplasmic vacuoles (lysosomes and autophagic vacuoles), appears at the eight-cell stage and grows pregressively stronger up to the blastocyst stage. Golgi-associated reaction for TPPase was detectable in oocytes, dropped in one-cell embryos and became negative in the two-cell embryos. The reaction for TPPase and IDPase was present in plasma membranes of oocytes and early embryos and appeared in the delimiting membrane of some cytoplasmic vesicles in eight-cell embryos. Some activity of IDPase was found in small segments of the ER at the morula and blastocyst stage. The observed results suggest that the lysosomes are the first organelles in early embryos showing activity of the marker enzymes of the phosphatase type, while the activity of other marker enzymes is mainly concentrated in the plasma membrane of blastomeres. It cannot be excluded, however, that positive reaction for TPPase and IDPase in the plasma membrane results from nonspecific action of other phosphatases.

摘要

在超微结构水平上,利用细胞化学方法研究了小鼠次级卵母细胞和植入前胚胎中细胞质磷酸酶(酸性磷酸酶(AcPase)作为溶酶体的标志物、焦磷酸酶(TPPase)作为高尔基体的标志物、核苷二磷酸酶(NDPase,又称肌苷二磷酸酶(IDPase))作为内质网(ER)的酶标志物)的外观和定位。可检测到的AcPase活性位于界定某些细胞质液泡(溶酶体和自噬泡)的膜的内表面,在八细胞期出现,并在囊胚期之前逐渐增强。卵母细胞中可检测到与高尔基体相关的TPPase反应,在单细胞胚胎中下降,在二细胞胚胎中变为阴性。TPPase和IDPase反应存在于卵母细胞和早期胚胎的质膜中,并在八细胞胚胎中某些细胞质小泡的界定膜中出现。在桑葚胚和囊胚期的内质网小片段中发现了IDPase的一些活性。观察结果表明,溶酶体是早期胚胎中最早显示磷酸酶类型标志物酶活性的细胞器,而其他标志物酶的活性主要集中在卵裂球的质膜中。然而,不能排除质膜中TPPase和IDPase的阳性反应是由其他磷酸酶的非特异性作用引起的。

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