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抑制多胺合成会降低鸡胚中胚层原代培养物的生长速率,并延迟分化表型的表达。

Inhibition of polyamine synthesis reduces the growth rate and delays the expression of differentiated phenotypes in primary cultures of embryonic mesoderm from chick.

作者信息

Löwkvist B, Oredsson S M, Holm I, Emanuelsson H, Heby O

出版信息

Cell Tissue Res. 1987 Jul;249(1):151-60. doi: 10.1007/BF00215429.

Abstract

Inhibition of polyamine synthesis in early chick embryos blocks their development at gastrulation. Analyses of arrested embryos show that mesodermal outgrowth and differentiation are drastically impaired. To study these effects in greater detail, we have used primary cultures of embryonic mesoderm from chick. The cultures were treated with alpha-difluoromethylornithine (DFMO), an enzyme-activated irreversible inhibitor of ornithine decarboxylase, the first and rate-limiting enzyme in polyamine synthesis. In control culture medium, mesodermal cells retained their in ovo outgrowth behavior and differentiation pattern. Addition of 10 mM DFMO to the culture medium, however, retarded attachment and outgrowth, and reduced the rate of proliferation of the mesodermal cells. Furthermore, the expression of differentiated phenotypes, such as beating heart tissue, erythroid cells, and adipocyte-like cells, was delayed. Simultaneous addition of 100 microM putrescine prevented or reduced the effects of DFMO, showing that these were indeed caused by polyamine deficiency. In the DFMO-treated mesoderm, DNA synthesis was markedly suppressed by the first day. Similar effects on RNA and protein synthesis developed at a later time. Our data suggest that a reduction in the concentrations of the polyamines decreases the rate of mesodermal cell proliferation, and as a consequence delays the expression of differentiated phenotypes.

摘要

抑制早期鸡胚中的多胺合成会在原肠胚形成阶段阻断其发育。对发育停滞的胚胎进行分析表明,中胚层的生长和分化受到严重损害。为了更详细地研究这些影响,我们使用了鸡胚中胚层的原代培养物。这些培养物用α-二氟甲基鸟氨酸(DFMO)处理,DFMO是鸟氨酸脱羧酶的一种酶激活不可逆抑制剂,鸟氨酸脱羧酶是多胺合成中的首个限速酶。在对照培养基中,中胚层细胞保持其在卵内的生长行为和分化模式。然而,向培养基中添加10 mM DFMO会延迟细胞贴壁和生长,并降低中胚层细胞的增殖速率。此外,分化表型如跳动的心脏组织、红细胞和脂肪细胞样细胞的表达也会延迟。同时添加100 μM腐胺可预防或减轻DFMO的作用,表明这些作用确实是由多胺缺乏引起的。在经DFMO处理的中胚层中,DNA合成在第一天就受到明显抑制。对RNA和蛋白质合成的类似影响在稍后时间出现。我们的数据表明,多胺浓度的降低会降低中胚层细胞的增殖速率,从而延迟分化表型的表达。

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