Title

Responses of fibroblasts to anchorage of dorsal extracellular matrix receptors

UMMS Affiliation

Department of Physiology

Publication Date

12-17-2004

Document Type

Article

Subjects

Acrylic Resins; Actins; Animals; Calcium; Cell Adhesion; Cell Differentiation; Cell Line; Cell Membrane; Cell Movement; Cell Proliferation; Cells, Cultured; Collagen; Cytoskeleton; Extracellular Matrix; Fibrinogen; Fibroblasts; Fibronectins; Gene Expression Regulation; Image Processing, Computer-Assisted; Mice; Microscopy, Fluorescence; Models, Biological; NIH 3T3 Cells; Pseudopodia; Signal Transduction; Stress, Mechanical; Transfection

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

Fibroblasts in 2D cultures differ dramatically in behavior from those in the 3D environment of a multicellular organism. However, the basis of this disparity is unknown. A key difference is the spatial arrangement of anchored extracellular matrix (ECM) receptors to the ventral surface in 2D cultures and throughout the entire surface in 3D cultures. Therefore, we asked whether changing the topography of ECM receptor anchorage alone could invoke a morphological response. By using polyacrylamide-based substrates to present anchored fibronectin or collagen on dorsal cell surfaces, we found that well spread fibroblasts in 2D cultures quickly changed into a bipolar or stellate morphology similar to fibroblasts in vivo. Cells in this environment lacked lamellipodia and large actin bundles and formed small focal adhesions only near focused sites of protrusion. These responses depend on substrate rigidity, calcium ion, and, likely, the calcium-dependent protease calpain. We suggest that fibroblasts respond to both spatial distribution and mechanical input of anchored ECM receptors. Changes in cell shape may in turn affect diverse cellular activities, including gene expression, growth, and differentiation, as shown in numerous previous studies.

Rights and Permissions

Citation: Proc Natl Acad Sci U S A. 2004 Dec 28;101(52):18024-9. Epub 2004 Dec 15. Link to article on publisher's site

DOI of Published Version

10.1073/pnas.0405747102

Related Resources

Link to Article in PubMed

Journal/Book/Conference Title

Proceedings of the National Academy of Sciences of the United States of America

PubMed ID

15601776