Center for Information Services and High Performance Computing, Dresden University of Technology, 01062 Dresden, Germany.
J Theor Biol. 2010 Jun 7;264(3):1077-88. doi: 10.1016/j.jtbi.2010.03.021. Epub 2010 Mar 19.
Many internal epithelial organs derive from cysts, which are tissues comprised of bent epithelial cell layers enclosing a lumen. Ion accumulation in the lumen drives water influx and consequently water accumulation and cyst expansion. Lumen-size recognition is important for the regulation of organ size. When lumen size and cyst size are not controlled, diseases can result; for instance, renal failure of the kidney. We develop a mechanistic mathematical model of lumen expansion in order to investigate the mechanisms for saturation of cyst growth. We include fluid accumulation in the lumen, osmotic and elastic pressure, ion transport and stretch-induced cell division. We find that the lumen volume increases in two phases: first, due to fluid accumulation stretching the cells, then in the second phase, the volume increase follows the increase in cell number until proliferation ceases as stretch forces relax. The model is quantitatively fitted to published data of in vitro cyst growth and predicts steady state lumen size as a function of the model parameters.
许多内部上皮器官源自于囊肿,这是一种由弯曲的上皮细胞层组成的组织,包裹着一个腔。腔内离子的积累会导致水的流入,从而导致水的积累和囊肿的扩张。腔室大小的识别对于器官大小的调节非常重要。当腔室大小和囊肿大小不受控制时,就会导致疾病,例如肾脏衰竭。我们开发了一种腔内扩张的机械数学模型,以研究囊肿生长饱和的机制。我们包括腔内的流体积累、渗透和弹性压力、离子转运和拉伸诱导的细胞分裂。我们发现腔室体积的增加分为两个阶段:首先,由于流体积累拉伸细胞,然后在第二阶段,体积的增加与细胞数量的增加保持一致,直到拉伸力松弛时增殖停止。该模型定量拟合了体外囊肿生长的已发表数据,并预测了稳态腔室大小作为模型参数的函数。