Potten C S, Loeffler M
Epithelial Biology, Paterson Institute, Christie Hospital & Holt Radium Institute, Manchester, England.
J Theor Biol. 1987 Aug 21;127(4):381-91. doi: 10.1016/s0022-5193(87)80136-4.
A comprehensive model has been formulated for the proliferative behaviour of the crypts of the small intestine based on individual cell to cell relationships rather than on the average effects of all cells. The model accommodates a wide range of cell kinetic data and provides an insight into the mechanisms involved in cell movement within the columnar sheet of cells and into the relationship between the stem cells and their progeny. The model permits the number of stem cells and transit generations to be estimated. The number of stem cells is predicted to be not less than 4 and not more than 16 per crypt with cell cycle times of between 12 and 32 h respectively. Certain conclusions can be drawn concerning the mechanisms involved in the initial cell displacements after cell division. The model also allows an estimation of parameters which cannot be measured directly such as the degree of cell generation disorder and the amount of dispersion of cells within a cell lineage.
基于个体细胞间的关系而非所有细胞的平均效应,已构建了一个关于小肠隐窝增殖行为的综合模型。该模型涵盖了广泛的细胞动力学数据,并深入洞察了细胞在柱状细胞层内移动所涉及的机制以及干细胞与其后代之间的关系。该模型允许估计干细胞的数量和过渡代数。预计每个隐窝的干细胞数量不少于4个且不超过16个,细胞周期时间分别在12至32小时之间。可以得出关于细胞分裂后初始细胞位移所涉及机制的某些结论。该模型还允许估计一些无法直接测量的参数,如细胞生成紊乱程度和细胞谱系内细胞的分散量。