Cdc42 is essential for the polarized movement and adhesion of human dental pulp stem cells

被引:7
作者
Li, Mingwei [1 ,2 ,3 ,4 ]
Ma, Liang [1 ,2 ,3 ,6 ]
Song, Bing [5 ]
Yu, Dingyi [7 ]
Xiao, Min [1 ,2 ,3 ]
Mei, Xiaohan [1 ,2 ,3 ]
Guo, Huihui [1 ,2 ,3 ]
Yu, Qing [1 ,2 ,3 ]
机构
[1] Fourth Mil Med Univ, Sch Stomatol, State Key Lab Mil Stomatol, Xian, Shaanxi, Peoples R China
[2] Fourth Mil Med Univ, Sch Stomatol, Natl Clin Res Ctr Oral Dis, Xian, Shaanxi, Peoples R China
[3] Fourth Mil Med Univ, Sch Stomatol, Shaanxi Key Lab Stomatol, Dept Operat Dent & Endodont, Xian, Shaanxi, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Hainan Branch, Dept Stomatol, Sanya, Hainan, Peoples R China
[5] Cardiff Univ, Sch Dent, Oral & Biomed Sci, Heath Pk, Cardiff CF14 4XY, S Glam, Wales
[6] 44 Hosp Chinese PLA, Dept Stomatol, Guiyang, Guizhou, Peoples R China
[7] Xi An Jiao Tong Univ, Coll Stomatol, Dept Clin 1, Xian, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Cell division control protein 42; Human dental pulp stem cells; Migration; Polarization; Adhesion; FAMILY SMALL GTPASES; RHO GTPASES; ACTIN; MIGRATION; MICROTUBULES; DYNAMICS; MOTILITY;
D O I
10.1016/j.archoralbio.2017.09.036
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: Stem cell-based tissue repair and regeneration require the regulation of cell migration and adhesion. As a regulator of cell polarization, Cdc42 (cell division control protein 42) plays a basic role at the initial stage of cell migration and adhesion. This study explores the effect of Cdc42 on the polarized migration and adhesion of hDPSCs (human dental pulp stem cells). Design: HDPSCs were isolated from extracted third molars and transfected with siRNA targeted against Cdc42. Scratch wound assays and transwell assays were performed to detect the migration of human dental pulp stem cells. Polarization assays were applied to explore the polarized movement of Golgi bodies and nuclei. Western blot was used to examine the expression of related proteins. Results: The expression of Cdc42 was knocked down by siRNA transfection, which inhibited the migration of hDPSCs in both the scratch wound assays and transwell assays. Meanwhile, the proportion of polarized hDPSCs during migration was also decreased, and the adhesion ability of hDPSCs was downregulated. Western blot demonstrated that these effects were dependent on FAK (focal adhesion kinase), beta-catenin and GSK3 beta (Glycogen synthase kinase-3 beta). Conclusion: Our study demonstrates that Cdc42 plays an essential role during the polarized movement and adhesion of hDPSCs.
引用
收藏
页码:104 / 112
页数:9
相关论文
共 42 条
[31]   Collective Cell Migration [J].
Rorth, Pernille .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2009, 25 :407-429
[32]   Focal adhesion kinase modulates tension signaling to control actin and focal adhesion dynamics [J].
Schober, Markus ;
Raghavan, Srikala ;
Nikolova, Maria ;
Polak, Lisa ;
Pasolli, H. Amalia ;
Beggs, Hilary E. ;
Reichardt, Louis F. ;
Fuchs, Elaine .
JOURNAL OF CELL BIOLOGY, 2007, 176 (05) :667-680
[33]   Dynamics of the Rho-family small GTPases in actin regulation and motility [J].
Spiering, Desiree ;
Hodgson, Louis .
CELL ADHESION & MIGRATION, 2011, 5 (02) :170-180
[34]   Targeting and transport: How microtubules control focal adhesion dynamics [J].
Stehbens, Samantha ;
Wittmann, Torsten .
JOURNAL OF CELL BIOLOGY, 2012, 198 (04) :481-489
[35]   Cdc42 in oncogenic transformation, invasion, and tumorigenesis [J].
Stengel, Kristy ;
Zheng, Yi .
CELLULAR SIGNALLING, 2011, 23 (09) :1415-1423
[36]   Current knowledge of the large RhoGAP family of proteins [J].
Tcherkezian, Joseph ;
Lamarche-Vane, Nathalie .
BIOLOGY OF THE CELL, 2007, 99 (02) :67-86
[37]   Cell migration at a glance [J].
Vicente-Manzanares, M ;
Webb, DJ ;
Horwitz, AR .
JOURNAL OF CELL SCIENCE, 2005, 118 (21) :4917-4919
[38]   Actin, microtubules and focal adhesion dynamics during cell migration [J].
Wehrle-Haller, B ;
Imhof, BA .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2003, 35 (01) :39-50
[39]   Polarised cell migration: intrinsic and extrinsic drivers [J].
Woodham, Emma F. ;
Machesky, Laura M. .
CURRENT OPINION IN CELL BIOLOGY, 2014, 30 :25-32
[40]   Gene targeting of Cdc42 and Cdc42GAP affirms the critical involvement of Cdc42 in filopodia induction, directed migration, and proliferation in primary mouse embryonic fibroblasts [J].
Yang, Linda ;
Wang, Lei ;
Zheng, Yi .
MOLECULAR BIOLOGY OF THE CELL, 2006, 17 (11) :4675-4685