期刊文献+

黏着斑-细胞骨架系统介导流体剪切力力转导研究进展 被引量:5

Roles of focal adhesion plaques and cytoskeleton in fluid shear stress-induced mechanotransduction
下载PDF
导出
摘要 黏着斑是将细胞外基质与细胞骨架联系起来的多蛋白聚集体,在力信号转化为细胞内化学信号、继而引发相应的生理或病理反应过程中发挥着重要作用。本文以黏着斑-细胞骨架系统为重点,总结了黏着斑介导的流体剪切力的力转导过程以及细胞骨架在此过程中的关键作用,介绍了黏着斑中参与胞内信号转导的重要蛋白,并讨论了黏着斑与其他力转导途径的联系,为更好理解剪切力和相关疾病间的关联以及临床药物的研发和疾病的治疗奠定了理论基础。 Focal adhesion plaques (FAPs) are multi-protein aggregates, which act as physical connections between extracellular matrix and cytoskeleton (CSK). FAPs and CSK play important roles in the conversion of mechanical signals into intracellular chemical signals followed by physiological and pathological responses. With focus on FAPs-CSK system, this review summarized the process of fluid shear stress-induced mechanotransduction and the roles of FAPs and CSK in this process in detail, introduced important proteins in FAPs, discussed the relationship between FAPs and other mechanotransduction pathways. The review established the theoretical foundation for understanding of the relationship between fluid shear stress and shear stress-related diseases, as well as development of clinical drug and treatment of these diseases.
出处 《医用生物力学》 EI CAS CSCD 北大核心 2014年第3期292-298,共7页 Journal of Medical Biomechanics
基金 国家自然科学基金资助项目(30970700,11032012)
关键词 黏着斑 细胞骨架 流体剪切力 力转导 Focal adhesion plaques Cytoskeleton Fluid shear stress Mechanotransduction
  • 相关文献

参考文献46

  • 1李德强,李德强,李德强,杨爱玲,汤亭亭,汤亭亭,卢建熙,卢建熙,郭雪岩,戴尅戎,戴尅戎,戴尅戎,戴尅戎.灌注式生物反应器中流体剪切力对大段组织工程化骨构建的作用[J].医用生物力学,2009,24(1):8-14. 被引量:5
  • 2Ingber DE.Cellular mechanotransduction:Putting all thepieces together again [J].FASEB J,2006,20(7):811-827.
  • 3Makino A,Prossnitz ER,Bunemann M,et al.G protein-coupled receptors serve as mechanosensors for fluid shearstress in neutrophils [J]. Am J Physiol Celt Physiol,2006,290(6):C1633-1639.
  • 4Vogel V.Mechanotransduction involving multimodular pro-teins:Converting force into biochemical signals [J].AnnuRev Biophys Biomol Struct,2006,35:459-488.
  • 5Schwartz MA.Integrins and extracellular matrix in mecha-notransduction [J].Cold Spring Harb Perspect Biol,2010,2(12):a005066.
  • 6Yamada KM,Geiger B.Molecular interactions in cell adhe-sion complexes [J].Curr Opin Cell Biol,1997,9(1):76-85.
  • 7Wozniak MA,Modzelewska K,Kwong L,et al.Focal ad-hesion regulation of cell behavior [J].Biochim Biophys Ac-ta,2004,1692(2-3):103-119.
  • 8Harburger DS,Calderwood DA.Integrin signalling at aglance [J].J Cell Sci,2009,122(Pt 2):159-163.
  • 9Zebda N,Dubrovskyi O,Birukov KG.Focal adhesion ki-nase regulation of mechanotransduction and its impact onendothelial cell functions [J].Microvasc Res,2012,83(1):71-81.
  • 10Friedland JC,Lee MH,Boettiger D.Mechanically activa-ted integrin switch controls alpha5beta1 function [J].Sci-ence,2009,323(5914):642-644.

二级参考文献85

  • 1Klein-Nulend J, van der Plas A, Semeins CM, etal. Sensitivityof osteocytes to biomechanical stress in vitro [J]. FASEB J, 1995, 9(5):441-445.
  • 2Owan I, Burr DB, Turner CH, et al. MechanotransducUon in bone: osteoblasts are more responsive to fluid forces than mechanical strain [J].Am J Physiol,1997,273(3 Pt 1 ):C810-815.
  • 3Smalt R, Mitchell FT, Howard RL, et al. Induction of NO and prostaglandin E2 in osteoblasts by wall-shear stress but not mechanical strain [J]. Am J Physiol, 1997,273(4 Pt 1 ):E751-758.
  • 4Martin I, Wendt D, Heberer M. The role of bioreactors in tissue engineering [J].Trends Biotechnol, 2004, 22 (2): 80-86.
  • 5Porter B, Z.auel R, Stockman H, et al. 3-D computational modeling of media flow through scaffolds in a perfusion bioreactor [J]. J Biom ech, 2005, 38 (3):543-549.
  • 6Chung CA, Chen CW, Chen CP, et al. Enhancement of cell growth in tissue-engineering constructs under direct perfusion: Modeling and simulation [J]. Biotechnol Bioeng, 2007,97(6):1603-1616.
  • 7Pierre J, Oddou C. Engineered bone culture in a perfusion bioreactor: a 2D computational study of stationary mass and momentum transport [J]. Comput Methods Biomech Biomed Engin, 2007, 10(6):429438.
  • 8Chung CA, Chen CP, Lin TH, et al. A compact computational model for cell construct development in perfusion culture [J]. Biotechnol Bioeng, 2008, 99(6):1535-1541.
  • 9Kreke MR, Goldstein AS. Hydrodynamic shear stimulates osteocalcin expression but not proliferation of bone marrow stem cells [J]. Tissue Eng, 2004, 10(5-6):780-788.
  • 10Weinbaum S, Cowin SC, Zeng Y. A model for the excitation of osteocytes by mechanical loading-induced bone fluid shear stresses [ J ]. J Biomech, 1994, 27 (3):339- 360.

共引文献27

同被引文献43

  • 1朱赴东,赵士芳,童晓艳,方进华.成骨细胞中NO及c-fos对流体剪切力的响应[J].浙江大学学报(医学版),2006,35(5):479-484. 被引量:5
  • 2丁柏,汪恭质,张晓铀,岳茗,曾育章,谭映军.模拟失重和超重刺激对体外培养成骨瘤细胞分裂、增殖影响的研究[J].航天医学与医学工程,1997,10(2):104-107. 被引量:15
  • 3丁波,黄姣,何斌.成骨生长肽对大鼠成骨细胞I型胶原蛋白的影响[J].重庆医科大学学报,2007,32(9):951-953. 被引量:9
  • 4Miwa M, Kozawa O, Tokuda H, et al. Effects of hyperg- ravity on proliferation and differentiation of osteoblast-like cells [J]. Bone Miner, 1991, 14(1):15-25.
  • 5Kawashima K, Shibata R, Negishi Y, et aL Stimulative effect of high-level hypergravity on differentiated functions of osteoblast-like ceils [ J ]. Ceil Struct Funct, 1998, 23 (4) : 221-2:29.
  • 6Furutsu M, Kawashima K, Negishi Y, et aL Bidirectional effects of hypergravity on the cell growth and differentiated functions of osteoblast-like ROS17/2. 8 cells[ J ]. Biol Pharm Bull, 2000, 23(10): 1258-1261.
  • 7van Loon J J, van Laar MC, Korterik JP, et aL An atomic force microscope operating at hypergravity for in situ meas- urement of cellular mechano-response [ J ]. J Microsc, 2009, 233(2): 234-243.
  • 8Kacena MA, Todd P, Gerstenfeld LC, et al. Experiments with osteoblasts cultured under hypergravity conditions [J]. Microgravity Sci Technol, 2004, 15(1) : 28-34.
  • 9Searby ND, Steele CR, Globus RK. Influence of increased mechanical loading by hypergravity on the microtubule cy- toskeleton and prostaglandin E2 release in primary osteo- blasts [ J ]. Am J Physiol Cell Physiol, 2005, 289 ( 1 ) : C148-158.
  • 10Kacena MA, Todd P, Gerstenfeld LC, et aL Experiments with osteoblasts cultured under varying orientations with respect to the gravity vector [ J ]. Cytotechnology, 2002, 39(3) : 147-154.

引证文献5

二级引证文献18

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部