摘要
目的:探讨LRRC4(leucine-rich repeats containing 4)通过SDF-1α/CXCR4(stromal cell-derivedfactor-1α/CXC receptor 4)对脑胶质瘤细胞侵袭迁移能力的影响。方法:将LRRC4基因转入脑胶质母细胞瘤U251细胞,分别通过RT-PCR实验、黏附实验、侵袭实验、细胞运动试验、划痕标记荧光染料示踪实验,研究SDF-1α干预前后LRRC4对U251细胞迁移能力的影响。结果:将LRRC4基因转入脑胶质瘤细胞U251,通过RT-PCR实验发现CXCR4的表达下调。用CXCR4的特异配体SDF-1α干预后,肿瘤黏附内皮实验、侵袭实验、细胞迁移实验、划痕标记染料示踪实验表明脑胶质瘤细胞迁移能力增强,LRRC4可以抑制细胞的这种侵袭迁移能力。SDF-1α能够改善细胞间的通讯能力,LRRC4可以进一步增强这种通讯能力。结论:SDF-1α/CXCR4的相互作用可以增强脑胶质瘤细胞U251的运动迁移能力,LRRC4基因可以通过调控SDF-1α/CXCR4生物学轴有效地抑制肿瘤细胞的侵袭迁移能力。
Objective To exolore the effect of LRRC4 on the mobility and invasion of glio-blastomas U251 cells through the SDF-1α/CXCR4 axis. Methods RT-PCR, transfiher cell invasion assay, adhesion assay, scraping test, scrape loading, and dye transfer assay were used to determine the effect of LRRC4 on U251 cells. Results SDF-1α could increase the invasion in U251 which expressed CXCR4. The reintroduction of LRRC4 in U251 cells could inhibit the expression of CXCR4. LRRC4 also inhibited the adhesion ability of U251 to ECV304 as well as the mobility and invasion ability in vitro, which was mediated by the SDF-1α/CXCR4 axis. Furthermore, LRRC4 could greatly enhance the gap junctional intercellar communication of U251 cells .Conclusion The reintroduction of LRRC4 in U251 cells can inhibit the expression of CXCRd and the SDF-1α/CXCR4 axis-mediated cell invasion in vitro.
出处
《中南大学学报（医学版）》
CAS
CSCD
北大核心
2007年第5期735-741,共7页
Journal of Central South University ：Medical Science
基金
国家重大科学研究计划(2006CB910502
2006CB910504)
中国博士后科学基金(20060400265)
国家自然科学基金(30770825)
湖南省自然科学基金(06JJ20080)~~
