Biomechanical approaches for studying integration of tissue structure and function in mammary epithelia

被引:19
作者
Alcaraz, J [1 ]
Nelson, CM [1 ]
Bissell, MJ [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, 1 Cyclotron Rd,MS 83-101, Berkeley, CA 94720 USA
关键词
microenvironment; mammary epithelial cells; structure-function; cell shape; cell biomechanics; 3D cultures;
D O I
10.1007/s10911-004-1406-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The structure and function of each individual mammary epithelial cell (MEC) is largely controlled by a bidirectional interchange of chemical and mechanical signals with the microenvironment. Most of these signals are tissue-specific, since they arise from the threedimensional (3D) tissue organization and are modulated during mammary gland development, maturation, pregnancy, lactation, and involution. Although the important role played by structural and mechanical signals in mammary cell and tissue function is being increasingly recognized, quantitative biomechanical approaches are still scarce. Here we review currently available biomechanical tools that allow quantitative examination of individual cells, groups of cells or full monolayers in two-dimensional cultures, and cells in 3D cultures. Current technological limitations and challenges are discussed, with special emphasis on their potential applications in MEC biology. We argue that the combination of biomechanical tools with current efforts in mathematical modeling and in cell and molecular biology applied to 3D cultures provides a powerful approach to unravel the complexity of tissue-specific structure-function relationships.
引用
收藏
页码:361 / 374
页数:14
相关论文
共 71 条
[1]   Cell culture: Biology's new dimension [J].
Abbott, A .
NATURE, 2003, 424 (6951) :870-872
[2]   Microrheology of human lung epithelial cells measured by atomic force microscopy [J].
Alcaraz, J ;
Buscemi, L ;
Grabulosa, M ;
Trepat, X ;
Fabry, B ;
Farré, R ;
Navajas, D .
BIOPHYSICAL JOURNAL, 2003, 84 (03) :2071-2079
[3]   Modulation of membrane traffic by mechanical stimuli [J].
Apodaca, G .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2002, 282 (02) :F179-F190
[4]   Cadherin interaction probed by atomic force microscopy [J].
Baumgartner, W ;
Hinterdorfer, P ;
Ness, W ;
Raab, A ;
Vestweber, D ;
Schindler, H ;
Drenckhahn, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) :4005-4010
[5]   Measurement of local viscoelasticity and forces in living cells by magnetic tweezers [J].
Bausch, AR ;
Möller, W ;
Sackmann, E .
BIOPHYSICAL JOURNAL, 1999, 76 (01) :573-579
[6]   Flexible substrata for the detection of cellular traction forces [J].
Beningo, KA ;
Wang, YL .
TRENDS IN CELL BIOLOGY, 2002, 12 (02) :79-84
[7]   Tissue architecture: the ultimate regulator of breast epithelial function - Commentary [J].
Bissell, MJ ;
Rizki, A ;
Mian, IS .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (06) :753-762
[8]   Polarity determination in breast tissue: desmosomal adhesion, myoepithelial cells, and laminin 1 [J].
Bissell, MJ ;
Bilder, D .
BREAST CANCER RESEARCH, 2003, 5 (02) :117-119
[9]  
Bissell MJ, 1999, CANCER RES, V59, p1757S
[10]   HOW DOES THE EXTRACELLULAR-MATRIX DIRECT GENE-EXPRESSION [J].
BISSELL, MJ ;
HALL, HG ;
PARRY, G .
JOURNAL OF THEORETICAL BIOLOGY, 1982, 99 (01) :31-68