Keng V W, Yagi H, Ikawa M, Nagano T, Myint Z, Yamada K, Tanaka T, Sato A, Muramatsu I, Okabe M, Sato M, Noguchi T
Graduate School of Bioagricultural Sciences, Chikusa-ku, Nagoya, 464-8601, Japan.
Biochem Biophys Res Commun. 2000 Oct 5;276(3):1155-61. doi: 10.1006/bbrc.2000.3548.
Disruption of the mouse Hex gene resulted in embryonic lethality around embryonic age (E) 10.5, due to no substantial liver formation. Expression of albumin was detectable in heterozygous (Hex(+/-)) but not in homozygous (Hex(-/-)) [corrected] embryos at E8.5. Instead of liver bud formation at E9.5, a liver-like capsule structure was observed in Hex(-/-) [corrected] embryos. In Hex(-/-) [corrected] mutant liver, we found no hepatocytes but no signs of apoptotic cell death in the area. Expression of transcription factors involved in hepatocyte differentiation, hepatocyte nuclear factor (Hnf)3beta, Hnf6, Hnf4alpha and Hnf1alpha, were restricted to the capsule and internal matrix-like structure in the mutant liver and expression of a subset of these factors were reduced. Hematopoiesis of monocytes was impaired in mutant embryos while erythroid lineage was unaffected. These results indicate that Hex plays an essential role in progenitor cells which commit to the hepatic endoderm and in the hematopoietic differentiation of the monocyte lineage.
小鼠Hex基因的破坏导致胚胎在胚胎期(E)10.5左右死亡,原因是没有实质性的肝脏形成。在E8.5时,杂合子(Hex(+/-))胚胎中可检测到白蛋白表达,而纯合子(Hex(-/-))胚胎中则未检测到。在E9.5时,Hex(-/-)胚胎未形成肝芽,而是观察到一个类似肝脏的囊状结构。在Hex(-/-)突变肝脏中,我们未发现肝细胞,但该区域也没有凋亡细胞死亡的迹象。参与肝细胞分化的转录因子,如肝细胞核因子(Hnf)3β、Hnf6、Hnf4α和Hnf1α,在突变肝脏中仅限于囊状结构和内部基质样结构表达,且这些因子中的一部分表达减少。突变胚胎中单核细胞的造血功能受损,而红系谱系未受影响。这些结果表明,Hex在定向分化为肝内胚层的祖细胞以及单核细胞谱系的造血分化中起着至关重要的作用。