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生长培养基和环磷酸腺苷类似物对环磷酸腺苷诱导的F9畸胎癌细胞分化的影响。

Effects of growth medium and cyclic AMP analogues on the cAMP-induced differentiation of F9 teratocarcinoma cells.

作者信息

Goldstein B, Kindregan H, Niles R M

机构信息

Department of Biochemistry, Boston University School of Medicine, Massachusetts 02118.

出版信息

In Vitro Cell Dev Biol. 1991 Feb;27A(2):158-62. doi: 10.1007/BF02631003.

Abstract

F9 teratocarcinoma cells differentiate into parietal endodermlike cells when treated with retinoic acid (RA) and cyclic AMP (cAMP). We have previously found that F9 cells can be induced to differentiate by treatment with cAMP in the absence of RA. In the course of determining why other investigators had failed to observe cAMP-induced differentiation, we found that the growth medium played an important role in determining the response of F9 cells to differentiating agents. When F9 cells were grown in minimal essential medium (MEM) and treated with either 8-bromo-cAMP (8BrcA) + 1-methyl, 3-isobutylxanthine (MIX), or dibutyryl cAMP (DBcA) + theophylline (T), they differentiated to parietal endodermlike cells without any requirement for exogenous RA. However, when F9 cells were grown in Dulbecco's modified Eagle's medium (DME), DBcA/T failed to induce differentiation alone and required exogenous RA to induce formation of parietal endoderm-like cells. 8BrcA/MIX alone was still able to induce some differentiation, although the extent was not as great as those cells grown in MEM. These results could not be explained by the different growth-promoting properties of the two culture media because there was no difference in the doubling time of F9 cells grown in either medium. Likewise, RA and cAMP both inhibited growth to the same extent in either medium. Inasmuch as almost all published reports on F9 cell differentiation have used DME as a growth medium, and RA with or without DBcA/T as the differentiating agents, these studies would not have had the appropriate conditions to detect the cAMP-induced differentiation of F9 cells.

摘要

当用视黄酸(RA)和环磷酸腺苷(cAMP)处理时,F9畸胎癌细胞会分化为滋养层内胚层样细胞。我们之前发现,在没有RA的情况下,用cAMP处理可诱导F9细胞分化。在确定其他研究者为何未能观察到cAMP诱导的分化过程中,我们发现生长培养基在决定F9细胞对分化剂的反应方面起着重要作用。当F9细胞在最低限度基本培养基(MEM)中生长并用8-溴环磷酸腺苷(8BrcAMP)+ 1-甲基-3-异丁基黄嘌呤(MIX)或二丁酰环磷酸腺苷(DBcAMP)+茶碱(T)处理时,它们可分化为滋养层内胚层样细胞,而无需任何外源性RA。然而,当F9细胞在杜尔贝科改良伊格尔培养基(DME)中生长时,单独使用DBcAMP/T无法诱导分化,需要外源性RA来诱导滋养层内胚层样细胞的形成。单独使用8BrcAMP/MIX仍能诱导一定程度的分化,尽管程度不如在MEM中生长的细胞。这两种培养基不同的促生长特性无法解释这些结果,因为在任何一种培养基中生长的F9细胞倍增时间没有差异。同样,RA和cAMP在任何一种培养基中对生长的抑制程度相同。鉴于几乎所有关于F9细胞分化的已发表报告都使用DME作为生长培养基,以及使用有或没有DBcAMP/T的RA作为分化剂,这些研究可能没有合适的条件来检测cAMP诱导的F9细胞分化。

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