Cellular electroporation induces dedifferentiation in intact newt limbs

被引:21
作者
Atkinson, Donald L.
Stevenson, Tamara J.
Park, Eon Joo
Riedy, Matthew D.
Milash, Brett
Odelberg, Shannon J.
机构
[1] Univ Utah, Hlth Sci Ctr, Dept Internal Med, Div Cardiol, Salt Lake City, UT 84132 USA
[2] Univ Utah, Dept Neurobiol & Anat, Salt Lake City, UT 84132 USA
[3] Univ Utah, Interdepartmental Program Neurosci, Salt Lake City, UT 84132 USA
[4] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT 84132 USA
关键词
dedifferentiation; cellular plasticity; regeneration; electric field; electroporation; Newt; Notophthalmus viridescens;
D O I
10.1016/j.ydbio.2006.07.027
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Newts have the remarkable ability to regenerate lost appendages including their forelimbs, hindlimbs, and tails. Following amputation of an appendage, the wound is rapidly closed by the migration of epithelial cells from the proximal epidermis. Internal cells just proximal to the amputation plane begin to dedifferentiate to form a pool of proliferating progenitor cells known as the regeneration blastema. We show that dedifferentiation of internal appendage cells can be initiated in the absence of amputation by applying an electric field sufficient to induce cellular electroporation, but not necrosis or apoptosis. The time course for dedifferentiation following electroporation is similar to that observed following amputation with evidence of dedifferentiation beginning at about 5 days postelectroporation and continuing for 2 to 3 weeks. Microarray analyses, real-time RT-PCR, and in situ hybridization show that changes in early gene expression are similar following amputation or electroporation. We conclude that the application of an electric field sufficient to induce transient electroporation of cell membranes induces a dedifferentiation response that is virtually indistinguishable from the response that occurs following amputation of newt appendages. This discovery allows dedifferentiation to be studied in the absence of wound healing and may aid in identifying genes required for cellular plasticity. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:257 / 271
页数:15
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