Biomechanical approaches for studying integration of tissue structure and function in mammary epithelia
被引:19
作者:
Alcaraz, J
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Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, 1 Cyclotron Rd,MS 83-101, Berkeley, CA 94720 USAUniv Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, 1 Cyclotron Rd,MS 83-101, Berkeley, CA 94720 USA
Alcaraz, J
[1
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Nelson, CM
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Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, 1 Cyclotron Rd,MS 83-101, Berkeley, CA 94720 USAUniv Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, 1 Cyclotron Rd,MS 83-101, Berkeley, CA 94720 USA
Nelson, CM
[1
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Bissell, MJ
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Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, 1 Cyclotron Rd,MS 83-101, Berkeley, CA 94720 USAUniv Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, 1 Cyclotron Rd,MS 83-101, Berkeley, CA 94720 USA
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
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.
机构:
Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Bissell, MJ
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Rizki, A
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Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Rizki, A
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Mian, IS
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Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
机构:
Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USAUniv Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
Bissell, MJ
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Bilder, D
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机构:Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
机构:
Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Bissell, MJ
;
Rizki, A
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h-index: 0
机构:
Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Rizki, A
;
Mian, IS
论文数: 0引用数: 0
h-index: 0
机构:
Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
机构:
Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USAUniv Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
Bissell, MJ
;
Bilder, D
论文数: 0引用数: 0
h-index: 0
机构:Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA