Dissecting cell adhesion architecture using advanced imaging techniques

TY - JOUR

T1 - Dissecting cell adhesion architecture using advanced imaging techniques

AU - Morton, Penny

AU - Parsons, Madeline

PY - 2011/7

Y1 - 2011/7

N2 - Cell adhesion to extracellular matrix proteins or to other cells is essential for the control of embryonic development, tissue integrity, immune function and wound healing. Adhesions are tightly spatially regulated structures containing over one hundred different proteins that coordinate both dynamics and signaling events at these sites. Extensive biochemical and morphological analysis of adhesion types over the past three decades has greatly improved understanding of individual protein contributions to adhesion signaling and, in some cases, dynamics. However, it is becoming increasingly clear that these diverse macromolecular complexes contain a variety of protein sub-networks, as well as distinct sub-domains that likely play important roles in regulating adhesion behavior. Until recently, resolving these structures, which are often less than a micron in size, was hampered by the limitations of conventional light microscopy. However, recent advances in optical techniques and imaging methods have revealed exciting insight into the intricate control of adhesion structure and assembly. Here we provide an overview of the recent data arising from such studies of cell: matrix and cell: cell contact and an overview of the imaging strategies that have been applied to study the intricacies and hierarchy of proteins within adhesions.

AB - Cell adhesion to extracellular matrix proteins or to other cells is essential for the control of embryonic development, tissue integrity, immune function and wound healing. Adhesions are tightly spatially regulated structures containing over one hundred different proteins that coordinate both dynamics and signaling events at these sites. Extensive biochemical and morphological analysis of adhesion types over the past three decades has greatly improved understanding of individual protein contributions to adhesion signaling and, in some cases, dynamics. However, it is becoming increasingly clear that these diverse macromolecular complexes contain a variety of protein sub-networks, as well as distinct sub-domains that likely play important roles in regulating adhesion behavior. Until recently, resolving these structures, which are often less than a micron in size, was hampered by the limitations of conventional light microscopy. However, recent advances in optical techniques and imaging methods have revealed exciting insight into the intricate control of adhesion structure and assembly. Here we provide an overview of the recent data arising from such studies of cell: matrix and cell: cell contact and an overview of the imaging strategies that have been applied to study the intricacies and hierarchy of proteins within adhesions.

U2 - 10.4161/cam.5.4.16915

DO - 10.4161/cam.5.4.16915

M3 - Article

VL - 5

SP - 351

EP - 359

JO - Cell Adhesion & Migration

JF - Cell Adhesion & Migration

IS - 4

M1 - N/A

ER -