南通大学学报(医学版)
南通大學學報(醫學版)
남통대학학보(의학판)
JOURNAL OF NANTONG UNIVERSITY(MEDICAL SCIENCES)
2014年
6期
469-471
,共3页
满莉丽%宋红花%王莹洁%朱子文%张青%王勇军
滿莉麗%宋紅花%王瑩潔%硃子文%張青%王勇軍
만리려%송홍화%왕형길%주자문%장청%왕용군
高迁移率族蛋白B1%坐骨神经%施万细胞%迁移
高遷移率族蛋白B1%坐骨神經%施萬細胞%遷移
고천이솔족단백B1%좌골신경%시만세포%천이
high mobility group protein B1%sciatic nerve%Schwann cell%migration
目的:研究周围神经损伤后高迁移率族蛋白B1(high mobility group protein B1,HMGB1)在损伤神经远侧端的细胞定位及表达变化,探讨HMGB1对施万细胞(Schwann cells,SCs)迁移特性的影响,阐明HMGB1功能作用的细胞学基础。方法:建立Sprague-Dawley(SD)大鼠坐骨神经损伤模型,采用免疫荧光组织双标化学染色观察神经损伤后HMGB1的定位和表达情况,新生1~3 d SD大鼠取材体外培养SCs并进行纯化,利用Transwell小室检测HMGB1对SCs迁移的影响。结果:大鼠坐骨神经中HMGB1和S100共定位,主要定位于细胞核内,损伤后远侧端HMGB1表达明显升高;体外培养的SCs经过纯化后排列整齐、胞体透亮,纯度可达95%以上,可用于后续体外试验;HMGB1蛋白能够促进SCs迁移。结论:HMGB1参与损伤坐骨神经远侧端SCs的功能调节。
目的:研究週圍神經損傷後高遷移率族蛋白B1(high mobility group protein B1,HMGB1)在損傷神經遠側耑的細胞定位及錶達變化,探討HMGB1對施萬細胞(Schwann cells,SCs)遷移特性的影響,闡明HMGB1功能作用的細胞學基礎。方法:建立Sprague-Dawley(SD)大鼠坐骨神經損傷模型,採用免疫熒光組織雙標化學染色觀察神經損傷後HMGB1的定位和錶達情況,新生1~3 d SD大鼠取材體外培養SCs併進行純化,利用Transwell小室檢測HMGB1對SCs遷移的影響。結果:大鼠坐骨神經中HMGB1和S100共定位,主要定位于細胞覈內,損傷後遠側耑HMGB1錶達明顯升高;體外培養的SCs經過純化後排列整齊、胞體透亮,純度可達95%以上,可用于後續體外試驗;HMGB1蛋白能夠促進SCs遷移。結論:HMGB1參與損傷坐骨神經遠側耑SCs的功能調節。
목적:연구주위신경손상후고천이솔족단백B1(high mobility group protein B1,HMGB1)재손상신경원측단적세포정위급표체변화,탐토HMGB1대시만세포(Schwann cells,SCs)천이특성적영향,천명HMGB1공능작용적세포학기출。방법:건립Sprague-Dawley(SD)대서좌골신경손상모형,채용면역형광조직쌍표화학염색관찰신경손상후HMGB1적정위화표체정황,신생1~3 d SD대서취재체외배양SCs병진행순화,이용Transwell소실검측HMGB1대SCs천이적영향。결과:대서좌골신경중HMGB1화S100공정위,주요정위우세포핵내,손상후원측단HMGB1표체명현승고;체외배양적SCs경과순화후배렬정제、포체투량,순도가체95%이상,가용우후속체외시험;HMGB1단백능구촉진SCs천이。결론:HMGB1삼여손상좌골신경원측단SCs적공능조절。
Objective:To investigate the localization and expression changes of high mobility group protein B1(HMGB1) fol-lowing sciatic nerve injury, and also to test the effect of HMGB1 on migration of Schwann cells(SCs) in attempt to clarify the functional basis of the cells. Methods:With the establishment of rat sciatic nerve injury model, immunohistochemistry method was used to study the localization and the expression changes of HMGB1. SCs were also isolated from newborn rat pups (with-in postnatal 1-3 d) and purified. Transwell was used to test the effect of HMGB1 on migration of SCs. Results: Immunohisto-chemistry demonstrated that HMGB1 colocalized with S100 positive cells in the distal segment with most of them colocalized in nucleus, the positive staining increased after sciatic nerve injury. The purified SCs were in regular morphology. Statistical data showed that purification of the cell reached up to 95%. Extracellular HMGB1 was able to promote the migration of SCs. Conclusion:HMGB1 is involved in the functional regulation of SCs after sciatic nerve injury.