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检测非洲爪蟾指间细胞死亡的策略:T3 加速、BMP 应用和间质细胞培养。

Strategies to detect interdigital cell death in the frog, Xenopus laevis: T3 accerelation, BMP application, and mesenchymal cell cultivation.

机构信息

Department of Biological Science, Faculty of Life and Environmental Science, Shimane University, Matsue, Shimane 690-8504, Japan.

出版信息

In Vitro Cell Dev Biol Anim. 2012 May;48(5):313-25. doi: 10.1007/s11626-012-9508-x. Epub 2012 May 12.

Abstract

Fates of digits in amniotes, i.e., free or webbed digits, are determined by the size of programmed interdigital cell death (ICD) area. However, no (or very few) cell death has thus far been observed in developing limb buds of non-amniotic terrestrial vertebrates including other anuran or urodela amphibians. We speculate that the undetectable situation of amphibian ICD is the result of their less frequency due to slow developmental speed characteristic to most amphibian species. Here, we present three strategies for detecting difficult-to-find ICD in the frog, Xenopus laevis. (1) Addition of triiodo-L-thyronine (T(3)) accelerated two to three times the limb development and increased two to four times the appearance frequency of vital dye-stainable cells in limb buds of the accelerated tadpoles (stage 54 to 55). (2) Application of human bone morphogenetic protein-4 to the autopods of tadpoles at stage 53 to 54 enhanced digital cartilage formation and induced vital dye-stainable cells around the enhanced digital cartilages within 2 d. (3) In cell culture, T(3) increased the chondrogenic and cell death activities of limb mesenchymal cells. The augmentation of both activities by T(3) was stronger in the forelimb cells than in the hindlimb cells. This situation is well coincided with the limb fates of non-webbed forelimbs and webbed hindlimbs in X. laevis adulthood. Collectively, all three approaches showed that it become possible to detect X. laevis ICD with appropriate strategies.

摘要

跗跖动物(例如,自由或蹼状的跗跖)的跗跖命运是由编程性的趾间细胞死亡(ICD)区域的大小决定的。然而,到目前为止,在包括其他无尾目或有尾目两栖动物在内的非羊膜陆生脊椎动物的发育肢体芽中,尚未观察到细胞死亡(或非常少)。我们推测,由于大多数两栖动物物种的发育速度较慢,因此检测不到两栖动物 ICD 的情况是由于其频率较低所致。在这里,我们提出了三种检测青蛙 Xenopus laevis 中难以发现的 ICD 的策略。(1)添加三碘甲状腺素(T(3))可使肢体发育加速两到三倍,并使加速的蝌蚪肢体芽中 vital 染料可染细胞的出现频率增加两到四倍(阶段 54 至 55)。(2)在阶段 53 至 54 将人骨形态发生蛋白-4应用于蝌蚪的前肢,可增强指骨软骨的形成,并在 2 天内诱导增强的指骨软骨周围出现 vital 染料可染细胞。(3)在细胞培养中,T(3)增加了肢体间充质细胞的软骨生成和细胞死亡活性。与后肢细胞相比,T(3)增强了前肢细胞的这两种活性。这种情况与 X. laevis 成年期非蹼状前肢和蹼状后肢的肢命运非常吻合。总之,所有三种方法都表明,使用适当的策略可以检测到 X. laevis ICD。

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