Yin Bin, Li Ke-han, An Tai, Chen Tao, Peng Xiao-zhong
National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100005, China.
Chin Med Sci J. 2010 Jun;25(2):100-4. doi: 10.1016/s1001-9294(10)60030-2.
To investigate the molecular mechanism of nectin-like molecule 1 (NECL1) inhibiting the migration and invasion of U251 glioma cells.
We infected U251 glioma cells with adeno-nectin-like molecule 1 (Ad-NECL1) or empty adenovirus (Ad). Transwell and wound healing assays were performed to observe the migration of U251 cells incubated with the cell supernatant from Ad-NECL1 or Ad infected U251 cells. DNA microarray was applied to screen the gene expression profile after the restoration of NECL1 in U251 glioma cell lines. The differential expression of osteopontin (OPN), a gene related to migration and invasion, was further analyzed with semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR), Western blot, and immunohistochemistry.
The restoration of NECL1 inhibited migration of U251 cells significantly (P<0.05). Altogether 195 genes were found differentially expressed by microarray, in which 175 were up-regulated and 20 down-regulated, including 9 extracellular matrix proteins involved in the migration of cells. Both mRNA and protein expressions of OPN, the most markedly reduced extracellular matrix protein, were found decreased in U251 cells after restoration of NECL1. Immunohistochemical assay also detected an increase of OPN in glioma tissues, related with the progressing of malignant grade.
A link might exist between NECL1 and the extracellular matrix protein OPN in inhibiting the migration and invasion of U251 glioma cells.
探讨nectin样分子1(NECL1)抑制U251胶质瘤细胞迁移和侵袭的分子机制。
用腺病毒-nectin样分子1(Ad-NECL1)或空腺病毒(Ad)感染U251胶质瘤细胞。进行Transwell实验和伤口愈合实验,以观察用Ad-NECL1或Ad感染的U251细胞的细胞上清液孵育后的U251细胞的迁移情况。应用DNA微阵列技术筛选U251胶质瘤细胞系中NECL1恢复后的基因表达谱。用半定量逆转录-聚合酶链反应(RT-PCR)、蛋白质免疫印迹法和免疫组织化学法进一步分析与迁移和侵袭相关的骨桥蛋白(OPN)基因的差异表达。
NECL1的恢复显著抑制了U251细胞的迁移(P<0.05)。通过微阵列共发现195个基因差异表达,其中175个上调,20个下调,包括9种参与细胞迁移的细胞外基质蛋白。在NECL1恢复后的U251细胞中,发现细胞外基质蛋白中最明显减少的OPN的mRNA和蛋白表达均下降。免疫组织化学检测还发现胶质瘤组织中OPN增加,且与恶性程度进展相关。
NECL1与细胞外基质蛋白OPN之间可能存在联系,共同抑制U251胶质瘤细胞的迁移和侵袭。