Schmidt G H, Winton D J, Ponder B A
Department of Cell Biology, Fraunhofer-Institute, Hannover, FRG.
Development. 1988 Aug;103(4):785-90. doi: 10.1242/dev.103.4.785.
We have previously shown that the epithelium of each adult intestinal crypt in chimaeric mice is derived from a single progenitor cell. Whether the crypts are monoclonal from the outset-that is, are formed by the proliferation of a single cell-or whether their formation is initiated by several cells was not known. Here we report that many crypts contain cells of both chimaeric genotypes in the neonatal period indicating a polyclonal origin at this stage of morphogenesis. The cellular organization of the early neonatal crypt is therefore different from that of the adult crypt, which includes a zone of 'anchored' stem cells above the crypt base. Within 2 weeks, however, the crypt progenitor cell and its descendants displace all other cells from the crypt and the crypt attains monoclonality. The distribution of enterocytes on chimaeric villi in the neonate shows a mottled pattern of mosaicism which is progressively replaced by coherent sheets of cells from the crypts, and within two weeks the orderly adult clonal pattern is established.
我们之前已经表明,嵌合小鼠中每个成年肠隐窝的上皮都源自单个祖细胞。隐窝从一开始是否就是单克隆的,即由单个细胞的增殖形成,或者它们的形成是否由几个细胞启动,这一点尚不清楚。在此我们报告,许多隐窝在新生期含有两种嵌合基因型的细胞,这表明在形态发生的这个阶段起源是多克隆的。因此,早期新生隐窝的细胞组织与成年隐窝不同,成年隐窝在隐窝底部上方包括一个“锚定”干细胞区。然而,在两周内,隐窝祖细胞及其后代将隐窝中的所有其他细胞取代,隐窝达到单克隆性。新生嵌合绒毛上肠细胞的分布呈现出斑驳的镶嵌模式,这种模式逐渐被来自隐窝的连贯细胞片所取代,并且在两周内建立起有序的成年克隆模式。