Sander M, Sussel L, Conners J, Scheel D, Kalamaras J, Dela Cruz F, Schwitzgebel V, Hayes-Jordan A, German M
Hormone Research Institute, University of California San Francisco, San Francisco, CA 94143-0534, USA.
Development. 2000 Dec;127(24):5533-40. doi: 10.1242/dev.127.24.5533.
Most insulin-producing beta-cells in the fetal mouse pancreas arise during the secondary transition, a wave of differentiation starting at embryonic day 13. Here, we show that disruption of homeobox gene Nkx6.1 in mice leads to loss of beta-cell precursors and blocks beta-cell neogenesis specifically during the secondary transition. In contrast, islet development in Nkx6. 1/Nkx2.2 double mutant embryos is identical to Nkx2.2 single mutant islet development: beta-cell precursors survive but fail to differentiate into beta-cells throughout development. Together, these experiments reveal two independently controlled pathways for beta-cell differentiation, and place Nkx6.1 downstream of Nkx2.2 in the major pathway of beta-cell differentiation.
大多数胎鼠胰腺中产生胰岛素的β细胞在二次转变期间出现,二次转变是从胚胎第13天开始的一波分化过程。在此,我们表明,小鼠中同源框基因Nkx6.1的破坏导致β细胞前体缺失,并特异性地在二次转变期间阻断β细胞新生。相比之下,Nkx6.1/Nkx2.2双突变胚胎中的胰岛发育与Nkx2.2单突变胰岛发育相同:β细胞前体存活,但在整个发育过程中未能分化为β细胞。这些实验共同揭示了两条独立控制的β细胞分化途径,并将Nkx6.1置于β细胞分化主要途径中Nkx2.2的下游。