细胞在小肠和大肠中的迁移表现出强烈的昼夜节律。

Epithelial cell biology Pub Date : 1994-01-01
J M Qiu, S A Roberts, C S Potten
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引用次数: 0

摘要

在一天中的6个不同时间,确定了小鼠小肠和大肠沿隐窝长度的每个位置的迁移速度估计。对隐窝的周长和长度也进行了测量。在小肠中观察到迁移速度随时间的显著变化(P < 0.001),在0900 h时最大为0.84个细胞位置(cp) /小时,在1700 h时最小为-0.46个细胞位置(cp) /小时,尽管负速度可能是人为的。24 h平均速度随细胞位置的变化而平稳上升,在细胞位置17(增殖区顶部附近)达到峰值0.45 cp/h。3HTdR标记细胞的百分比(最小30.8%,最大38.3%,P < 0.001)和隐窝周长(最小16.9个细胞,最大17.9个细胞,P = 0.003)的变化更为温和。大肠内的迁移速度不太确定,24小时平均迁移速度峰值(0.26 cp/h)出现在细胞位置10。在这个位置检测到显著的昼夜节律变化(最小-0.39 cp/h,最大0.75 cp/h, P = 0.006)。标记细胞百分比的变化(最小9.4%,最大22.3%,P < 0.001)和隐窝周长(最小18.3个细胞,最大19.2个细胞,P < 0.001)。在这两种组织中,这表明细胞增殖率的适度变化与隐窝细胞数量的变化相结合,可以解释隐窝输出量的大幅变化,并且隐窝几何形状变化的蓄水池效应是控制肠道细胞数量维持过程的重要组成部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell migration in the small and large bowel shows a strong circadian rhythm.

Migration velocity estimates have been determined at each position along the crypt length for both the small and large intestine of the mouse at 6 different times of the day. Measurements also have been made of crypt circumference and length. Dramatic, and significant (P < 0.001), changes in migration velocity as a function of time of day were observed in the small intestine with a maximum 0.84 cell positions (cp) per hour at 0900 h and a minimum of -0.46 cp/h at 1700 h, although the negative velocity was probably artefactual. The 24-h mean velocity rose smoothly as a function of cell position to a peak of 0.45 cp/h at cell position 17 (around the top of the proliferative zone). Much more modest changes were seen in the percent of 3HTdR labelled cells (minimum 30.8%, maximum 38.3%, P < 0.001) and crypt circumference (minimum 16.9 cells, maximum 17.9 cells, P = 0.003). The migration velocity was rather less well determined in the large intestine with a peak in the 24-h mean velocity (0.26 cp/h) occurring at cell position 10. At this position significant circadian variation was detected (minimum -0.39 cp/h, maximum 0.75 cp/h, P = 0.006). Changes were seen in the percent of labelled cells (minimum 9.4%, maximum 22.3%, P < 0.001) and crypt circumference (minimum 18.3 cells, maximum 19.2 cells, P < 0.001). In both tissues it is suggested that the combination of the modest changes in cell proliferation rates in conjunction with the changes in crypt cell number can account for the large amplitude in variation of crypt output, and that the reservoir effects of changes in crypt geometry are an essential part of the process governing the maintenance of intestinal cell numbers.

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