Pax4 paired domain mediates direct protein transduction into mammalian cells

被引:24
作者
Lu, Jun
Li, Ge
Lan, Michael S.
Zhang, Shuyu
Fan, Weiwei
Wang, Hongwei
Lu, Daru
机构
[1] Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[2] Louisiana State Univ, Hlth Sci Ctr, Dept Pediat, Res Inst Children,Childrens Hosp, New Orleans, LA 70118 USA
关键词
D O I
10.1210/en.2007-0636
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pax4, a paired-box transcription factor, is a key regulator of pancreatic islet cell growth and differentiation. Here, we report for the first time that the Pax4 protein can permeate into various cell types including pancreatic islets. The paired domain of Pax4 serves as a novel protein transduction domain (PTD). The Pax4 protein can transduce in a dose-and time-dependent manner. The cellular uptake of Pax4 PTD can be completely blocked by heparin, whereas cytochalasin D and amiloride were partially effective in blocking the Pax4 protein entry. Transduced intact Pax4 protein functions similarly to the endogenous Pax4. It inhibits the Pax6 mediated transactivation and protects Min6 cells against TNF alpha-induced apoptosis. These data suggest that Pax4 protein transduction could be a safe and valuable strategy for protecting islet cell growth in culture from apoptosis and promoting islet cell differentiation.
引用
收藏
页码:5558 / 5565
页数:8
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