Loss and recovery of the blood-nerve barrier in the rat sciatic nerve after crush injury are associated with expression of intercellular junctional proteins

被引:54
作者
Hirakawa, H
Okajima, S
Nagaoka, T
Takamatsu, T
Oyamada, M [1 ]
机构
[1] Kyoto Prefectural Univ Med, Dept Pathol & Cell Regulat, Kamikyo Ku, Kyoto 6028566, Japan
[2] Kyoto Prefectural Univ Med, Dept Orthoped Surg, Kyoto 6028566, Japan
基金
日本学术振兴会;
关键词
adherens junction; blood-nerve barrier; cadherin; claudin; connexin; crush injury; gap junctions; occludin; peripheral nerve; tight junctions;
D O I
10.1016/S0014-4827(02)00035-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The blood-nerve barrier in peripheral nerves is important for maintaining the environment for axons. Breakdown of the barrier by nerve injury causes various pathologies. We hypothesized that the breakdown and recovery of the blood-nerve barrier after injury are associated with the changes in the expression of intercellular junctional proteins. To test this hypothesis, we induced crush injuries in the rat sciatic nerve by ligation and analyzed spatiotemporal changes of claudin-1, claudin-5, occludin, VE-cadherin, and connexin43 by immunoconfocal microscopy and morphometry and compared them with changes in the permeability of the blood-nerve barrier by intravenous and local administration of Evans blue-albumin (EBA). On day 1 after removal of the ligature EBA leaked into the connective tissue in the endoneurium and then the leakage gradually decreased and disappeared on day 7. On day I claudin-1, claudin-5, occludin, VE-cadherin, and connexin43 had totally disappeared from the perineurium and endoneurium. Thereafter, claudin-1, claudin-5, occludin, and VE-cadherin recovered from day 2, whereas connexin43 was redetected on day 5. These results indicate that the breakdown and following recovery of the blood-nerve barrier are closely associated with changes in the expression of claudins, occludin, VE-cadherin, and connexin43 and that the recovery time course is similar but nonidentical. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:196 / 210
页数:15
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