Mechanobiology and the Microcirculation: Cellular, Nuclear and Fluid Mechanics

被引:49
作者
Dahl, Kris Noel [1 ]
Kalinowski, Agnieszka [1 ]
Pekkan, Kerem [1 ]
机构
[1] Carnegie Mellon Univ, Dept Biomed Engn, Dept Chem Engn, Pittsburgh, PA 15213 USA
关键词
Nuclear mechanics; Hutchinson-Gilford progeria syndrome; computational fluid dynamics; rheology; lamins; SHEAR-STRESS; LAMIN-A; ENDOTHELIAL-CELLS; GENE-EXPRESSION; BLOOD-FLOW; IN-VITRO; DYNAMIC SIMULATION; SCANNING-ELECTRON; TERMINAL REGION; ACTIVATION;
D O I
10.1111/j.1549-8719.2009.00016.x
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
P>Endothelial cells are stimulated by shear stress throughout the vasculature and respond with changes in gene expression and by morphological reorganization. Mechanical sensors of the cell are varied and include cell surface sensors that activate intracellular chemical signaling pathways. Here, possible mechanical sensors of the cell including reorganization of the cytoskeleton and the nucleus are discussed in relation to shear flow. A mutation in the nuclear structural protein lamin A, related to Hutchinson-Gilford progeria syndrome, is reviewed specifically as the mutation results in altered nuclear structure and stiffer nuclei; animal models also suggest significantly altered vascular structure. Nuclear and cellular deformation of endothelial cells in response to shear stress provides partial understanding of possible mechanical regulation in the microcirculation. Increasing sophistication of fluid flow simulations inside the vessel is also an emerging area relevant to the microcirculation as visualization in situ is difficult. This integrated approach to study-including medicine, molecular and cell biology, biophysics and engineering-provides a unique understanding of multi-scale interactions in the microcirculation.
引用
收藏
页码:179 / 191
页数:13
相关论文
共 128 条
[1]
Nuclear deformation characterizes Werner syndrome cells [J].
Adelfalk, C ;
Scherthan, H ;
Hirsch-Kauffmann, M ;
Schweiger, M .
CELL BIOLOGY INTERNATIONAL, 2005, 29 (12) :1032-1037
[2]
ALI SS, 1984, CELL TISSUE RES, V235, P675
[3]
Micro-scale dynamic simulation of erythrocyte-platelet interaction in blood flow [J].
AlMomani, T. ;
Udaykumar, H. S. ;
Marshall, J. S. ;
Chandran, K. B. .
ANNALS OF BIOMEDICAL ENGINEERING, 2008, 36 (06) :905-920
[4]
Computational fluid dynamic simulation of aggregation of deformable cells in a shear flow [J].
Bagchi, P ;
Johnson, PC ;
Popel, AS .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 2005, 127 (07) :1070-1080
[5]
A flow-activated chloride-selective membrane current in vascular endothelial cells [J].
Barakat, AI ;
Leaver, EV ;
Pappone, PA ;
Davies, PF .
CIRCULATION RESEARCH, 1999, 85 (09) :820-828
[6]
PREDICTION OF BLOOD FLOW IN TUBES WITH DIAMETERS AS SMALL AS 29-MU [J].
BARBEE, JH ;
COKELET, GR .
MICROVASCULAR RESEARCH, 1971, 3 (01) :17-&
[7]
[8]
Interaction of the C-terminal region of the Gγ protein with model membranes [J].
Barcelo, Francisca ;
Prades, Jesus ;
Encinar, Jose Antonio ;
Funari, Sergio S. ;
Voegler, Oliver ;
Gonzalez-Ros, Jose Manuel ;
Escriba, Pablo V. .
BIOPHYSICAL JOURNAL, 2007, 93 (07) :2530-2541
[9]
BASSINGHTHWAIGHTE JB, 1990, ANN NY ACAD SCI, V591, P392
[10]
Boisseau MR, 2005, CLIN HEMORHEOL MICRO, V33, P201