Mechanism of age-dependent involution in embryonic chick notochords.

Experientia Pub Date : 1996-07-15 DOI:10.1007/BF01925574
E Ghanem, M Cornelissen, H Thierens, L De Ridder
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引用次数: 0

Abstract

To study the possible mechanism of the age-dependent involution of the notochord, isolated mesenchyme-free notochords of chick embryos were cultured in vitro and compared with their counterparts in vivo. Two different aspects were evaluated: (1) DNA synthesis measured by [3H]thymidine incorporation and visualized by autoradiography and (2) cell death quantified by counting the number of pyknotic nuclei. The results demonstrate that [3H]thymidine uptake by notochords shows an age-dependent decrease in vitro as well as in vivo. The number of [3H]thymidine-labelled notochord cells, however, is higher in vitro than in vivo. At the same time, there is an age-dependent increase in pyknosis in the notochord in vivo and in vitro. So, during the aging process, the number of both pyknotic nuclei and of [3H]thymidine-labelled nuclei suggest a high turnover of notochord cells in vitro. From these results, we can conclude that the process of involution in aging notochord seems to be controlled by a programmed intrinsic process, which might be influenced partially by the microenvironment in vivo.

鸡胚脊索年龄依赖性复归的机制。
为了研究年龄依赖性脊索退化的可能机制,我们在体外培养离体无间质鸡胚脊索,并与体内脊索进行比较。两个不同的方面进行评估:(1)DNA合成测量[3H]胸苷结合和放射自显影(2)细胞死亡量化通过计数缩缩细胞核的数量。结果表明,脊索对[3H]胸腺嘧啶的摄取在体内和体外均呈年龄依赖性减少。然而,[3H]胸腺嘧啶标记的脊索细胞的数量在体外比在体内高。同时,脊索固缩在体内和体外均呈年龄依赖性增加。因此,在衰老过程中,收缩核和[3H]胸腺嘧啶标记核的数量表明体外脊索细胞的高周转率。综上所述,我们认为脊索衰老过程似乎是由一个程序化的内在过程控制的,该过程可能部分受到体内微环境的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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