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[大鼠心室细胞层受损后培养物中的再生与DNA合成]

[Regeneration and DNA synthesis in cultures of rat heart ventricles after damage to the cellular layer].

作者信息

Borisov A B, Khaĭrutdinova Iu A

出版信息

Arkh Anat Gistol Embriol. 1986 Sep;91(9):62-7.

PMID:3789934
Abstract

By means of the 3H-thymidine radioautography method replicative activity of myocytes and other cells in a dense layer of cellular culture of the traumatized ventricular myocardium has been studied in newborn (2-3-day-old) rats after lesion of the myocardium. Proliferation of the non-muscular cells is sharply suppressed after the cellular layer formation: their labelling index (LI) is 5.7 +/- 2.2% on the 8th day. Simultaneously, LI of unicellular myocytes is 25 +/- 6%, and that of binuclear ones, specific for the myocardium of mature animals is 6.4 +/- 2.9%. That demonstrates autonomy of DNA synthesis in myocytes from its suppression in the surrounding non-muscular cells. For 1-2 days after trauma intensive migration of fibroblasts into the wound is observed; they are often oriented perpendicularly to the edges of the cellular layer. There is an activation of DNA synthesis in the non-muscular cells in the wound area (in 20 h after the lesion LI is 73.4 +/- 1.7%) and in the layer edge directed to the wound LI is 23.9 +/- 0.0%, while in the depth of the zone situating close to the wound their LI is 7.8 +/- 2.4%. The replicative activity of mononuclear cardiomyocytes in the zone mentioned increases very weakly (LI 32 +/- 5%), and LI of binuclear ones is practically unchanged (6.1 +/- 2.3%). Karyo-kinetic activity is estimated by amount of binuclear cardiomyocytes and in the zone near the wound, in comparison to that in an intact layer, it does not change (35 +/- 3% and 34.4 +/- 2.5%).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用³H-胸腺嘧啶核苷放射自显影法,对新生(2 - 3日龄)大鼠创伤性心室心肌细胞培养致密层中的心肌细胞和其他细胞的复制活性进行了研究。细胞层形成后,非肌肉细胞的增殖受到明显抑制:第8天时其标记指数(LI)为5.7±2.2%。同时,单细胞心肌细胞的LI为25±6%,而成熟动物心肌特有的双核心肌细胞的LI为6.4±2.9%。这表明心肌细胞中DNA合成具有自主性,不受周围非肌肉细胞抑制的影响。创伤后1 - 2天,观察到成纤维细胞大量迁移至伤口处;它们常垂直于细胞层边缘排列。伤口区域的非肌肉细胞DNA合成激活(损伤后20小时LI为73.4±1.7%),朝向伤口的层边缘处LI为23.9±0.0%,而靠近伤口区域深处的LI为7.8±2.4%。上述区域单核心肌细胞的复制活性增加非常微弱(LI为32±5%),双核心肌细胞的LI实际上未改变(6.1±2.3%)。通过双核心肌细胞数量评估核分裂活性,与完整层相比,伤口附近区域未发生变化(分别为35±3%和34.4±2.5%)。(摘要截断于250字)

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