Cell distribution during mouse secondary palate closure. II. Mesenchymal cells.

L L Brinkley, F L Bookstein
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Abstract

The patterns of distribution of both total mesenchymal cells and the ratios of [3H]thymidine-labelled to total cells were mapped during secondary palatal shelf reorientation in vivo and in vitro. Smoothed spatial averaging, a computer-assisted method which takes into account the positions of all cells across an entire histological section of the shelf, was employed. Changes in shelf cross-sectional area and cell size were also measured. Three shelf regions, anterior and posterior presumptive hard and presumptive soft palate, were studied at developmental stages which were 30, 24 and 18 h prior to expected in vivo elevation, after in vivo reorientation and during the course of in vitro reorientation. Region-specific patterns of cell distribution change with shelf reorientation. These changes were observable within 6 h. Increases in cell number by cell division may enhance some high local cell densities, but cannot account for decreases in cell density. Increase in cell size is not a factor in decreasing cell density, nor is cell death. Displacement of cells by expansion of the extracellular matrix may be involved.

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小鼠次级上颚闭合过程中的细胞分布。2间充质细胞。
绘制了在体内和体外二次腭架重定向过程中间充质细胞总数的分布模式和[3H]胸腺嘧啶标记的细胞总数的比例。平滑空间平均,一种计算机辅助的方法,考虑到所有细胞在架子的整个组织学部分的位置,被采用。还测量了架子横截面积和细胞大小的变化。在预期体内提升前30、24和18小时、体内重新定位后和体外重新定位过程中,研究了三个架子区域,即前、后推定硬腭和推定软腭。区域特定的细胞分布模式随着架子的重新定位而改变。这些变化在6小时内可以观察到。细胞分裂引起的细胞数量的增加可能会增加一些高的局部细胞密度,但不能解释细胞密度的降低。细胞大小的增加不是降低细胞密度的一个因素,细胞死亡也不是。细胞外基质的扩张可能导致细胞移位。
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