Noncanonical role of transferrin receptor 1 is essential for intestinal homeostasis

被引:78
作者
Chen, Alan C. [1 ]
Donovan, Adriana [2 ]
Ned-Sykes, Renee [3 ]
Andrews, Nancy C. [1 ,4 ]
机构
[1] Duke Univ, Sch Med, Dept Pharmacol & Canc Biol, Durham, NC 27705 USA
[2] Scholar Rock, Div Pharmacol & Preclin Biol, Cambridge, MA 02142 USA
[3] Ctr Dis Control & Prevent, Div Lab Syst, Ctr Surveillance Epidemiol & Lab Serv, Atlanta, GA 30333 USA
[4] Duke Univ, Sch Med, Dept Pediat, Durham, NC 27705 USA
基金
美国国家卫生研究院;
关键词
transferrin receptor; intestinal epithelium; epithelial-mesenchymal transition; homeostasis; stem cell; EPITHELIAL-MESENCHYMAL TRANSITION; MOLECULAR-MECHANISMS; IRON-METABOLISM; BREAST-CANCER; EXPRESSION; CELLS; PHOSPHORYLATION; NOTCH; MICE; WNT;
D O I
10.1073/pnas.1511701112
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Transferrin receptor 1 (Tfr1) facilitates cellular iron uptake through receptor-mediated endocytosis of iron-loaded transferrin. It is expressed in the intestinal epithelium but not involved in dietary iron absorption. To investigate its role, we inactivated the Tfr1 gene selectively in murine intestinal epithelial cells. The mutant mice had severe disruption of the epithelial barrier and early death. There was impaired proliferation of intestinal epithelial cell progenitors, aberrant lipid handling, increased mRNA expression of stem cell markers, and striking induction of many genes associated with epithelial-to-mesenchymal transition. Administration of parenteral iron did not improve the phenotype. Surprisingly, however, enforced expression of a mutant allele of Tfr1 that is unable to serve as a receptor for iron-loaded transferrin appeared to fully rescue most animals. Our results implicate Tfr1 in homeostatic maintenance of the intestinal epithelium, acting through a role that is independent of its iron-uptake function.
引用
收藏
页码:11714 / 11719
页数:6
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