Duvillié Bertrand, Attali Myriam, Bounacer Ali, Ravassard Philippe, Basmaciogullari Annie, Scharfmann Raphael
Université Paris-Descartes, Faculté de Médecine, Institut National de la Santé et de la Recherche Médicale, E363, Hôpital Necker, Paris, France.
Diabetes. 2006 Mar;55(3):582-9. doi: 10.2337/diabetes.55.03.06.db05-0839.
The importance of mesenchymal-epithelial interactions in the proliferation of pancreatic progenitor cells is well established. Here, we provide evidence that the mesenchyme also controls the timing of beta-cell differentiation. When rat embryonic pancreatic epithelium was cultured without mesenchyme, we found first rapid induction in epithelial progenitor cells of the transcription factor neurogenin3 (Ngn3), a master gene controlling endocrine cell-fate decisions in progenitor cells; then beta-cell differentiation occurred. In the presence of mesenchyme, Ngn3 induction was delayed, and few beta-cells developed. This effect of the mesenchyme on Ngn3 induction was mediated by cell-cell contacts and required a functional Notch pathway. We then showed that associating Ngn3-expressing epithelial cells with mesenchyme resulted in poor beta-cell development via a mechanism mediated by soluble factors. Thus, in addition to its effect upstream of Ngn3, the mesenchyme regulated beta-cell differentiation downstream of Ngn3. In conclusion, these data indicate that the mesenchyme controls the timing of beta-cell differentiation both upstream and downstream of Ngn3.
间充质-上皮相互作用在胰腺祖细胞增殖中的重要性已得到充分证实。在此,我们提供证据表明间充质也控制β细胞分化的时间。当在没有间充质的情况下培养大鼠胚胎胰腺上皮时,我们首先发现上皮祖细胞中转录因子神经生成素3(Ngn3)迅速诱导,Ngn3是控制祖细胞内分泌细胞命运决定的主基因;然后发生β细胞分化。在有间充质存在的情况下,Ngn3诱导延迟,很少有β细胞发育。间充质对Ngn3诱导的这种作用是由细胞间接触介导的,并且需要功能性Notch信号通路。然后我们表明,将表达Ngn3的上皮细胞与间充质联合,通过可溶性因子介导的机制导致β细胞发育不良。因此,除了在Ngn3上游的作用外,间充质还在Ngn3下游调节β细胞分化。总之,这些数据表明间充质在Ngn3的上游和下游均控制β细胞分化的时间。