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小鼠胚胎肢芽在体外直接暴露于5-溴脱氧尿苷及其对软骨形成的影响:在发育的连续阶段对类似物的抗性增加。

Direct exposure of mouse embryonic limb-buds to 5-bromodeoxyuridine in vitro and its effect on chondrogenesis: increasing resistance to the analog at successive stages of development.

作者信息

Agnish N D, Kochhar D M

出版信息

J Embryol Exp Morphol. 1976 Dec;36(3):639-52.

PMID:1010983
Abstract

The inhibitory effect of 5-bromodeoxyuridine (BudR) - an analog of thymidine - on embryonic mouse limb-buds was studied in vitro employing an organ-culture system. The effect was found to be dose-related and also depended on the developmental stage of the donor embryos. Limbs at an early stage development (early 11 th-day embryos, somite stage 26-29) were extremely sensitive to the analog. Treatment with low levels (2-4 mug/ml) and for a relatively short period of time in cluture (2-3 days) completely and irreversibly suppressed chondrogenesis in these explants. Limbs from older embryos (somite stage 40 and up) were found to be much less sensitive to the inhibitory effect of the drug; a prolonged exposure to a much higher dose (100-150 mug/ml) resulted in an incomplete suppression of chondrogesesis. Only a 20% inhibition was observed in the cultures of limbs from mid-13th-day mouse embryos. After continuous growth in vitro, the limbs became progressively resistent to the analog and towards the end of the culture period had become refractory to the drug. The time of complete insensitivity appeared earlier in the cures of the limbs taken from older embryos than in the explants of youngerlimbs. These studies show that as limbs continue to differentiate in vivo or in vitro, they become increasingly resistent to the inhibitory effect of BudR in at least as far as the effect on the process of chondrogenesis is concerned. It is suggested that the relative sensitivity or insensitivity to the inhibitory effect of BudR may prove to be a useful parameter in evaluating the developmental stage of an organ.

摘要

利用器官培养系统在体外研究了胸腺嘧啶核苷类似物5-溴脱氧尿苷(BudR)对小鼠胚胎肢芽的抑制作用。发现该作用与剂量相关,并且还取决于供体胚胎的发育阶段。处于早期发育阶段(第11天早期胚胎,体节阶段26 - 29)的肢芽对该类似物极其敏感。在培养中用低水平(2 - 4微克/毫升)并处理相对较短时间(2 - 3天)能完全且不可逆地抑制这些外植体中的软骨形成。发现来自较老胚胎(体节阶段40及以上)的肢芽对该药物的抑制作用敏感性低得多;长时间暴露于高得多的剂量(100 - 150微克/毫升)导致软骨形成的抑制不完全。在第13天中期小鼠胚胎肢芽培养物中仅观察到20%的抑制。在体外持续生长后,肢芽对该类似物逐渐产生抗性,并且在培养期结束时对该药物变得不敏感。完全不敏感的时间在取自较老胚胎的肢芽培养物中比在较年轻肢芽的外植体中出现得更早。这些研究表明,随着肢芽在体内或体外继续分化,至少就对软骨形成过程的影响而言,它们对BudR的抑制作用越来越有抗性。有人提出,对BudR抑制作用的相对敏感性或不敏感性可能被证明是评估器官发育阶段的一个有用参数。

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