Loss of Hoxa5 gene function in mice perturbs intestinal maturation

被引:48
作者
Aubin, J
Chailler, P
Menard, D
Jeannotte, L
机构
[1] Univ Laval, Ctr Rech Cancerol, CHU Quebec, Quebec City, PQ G1R 2J6, Canada
[2] Univ Sherbrooke, Fac Med, Dept Anat & Biol Cellulaire, Grp Conseil Rech Med Canada Dev Funct & Physiopat, Sherbrooke, PQ J1H 5N4, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1999年 / 277卷 / 05期
关键词
Hox gene expression; intestinal enzymes; gut morphogenesis; regional specification; epithelial-mesenchymal interactions;
D O I
10.1152/ajpcell.1999.277.5.C965
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Hox: gene family of transcription factors constitutes candidate regulators in the molecular cascade of events that governs establishment of normal terminal differentiation along the duodenum to colon axis. One member of this family, Hoxa5, displays a dynamic pattern of expression during gut development. Hoxa6 transcripts are present in midgut mesenchyme at the time of remodeling, supporting a role for this gene in digestive tract specification. To study the role of Hoxa5 in proper intestinal development and maturation, we examined whether Hoxa5 mutant mice exhibit any defect in this process. We report here that even though Hoxa5 is not required for midgut morphogenesis, its loss of function perturbs the acquisition of adult mode of digestion, which normally is temporally coordinated with the process of-spontaneous weaning. Impaired maturation of the digestive tract might be related to altered specification of intestinal epithelial cells. Our findings provide evidence that Hoxa5 expression in the gut mesoderm is important for the region-specific differentiation of the adjacent endoderm.
引用
收藏
页码:C965 / C973
页数:9
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