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John C. Angello

Researcher at University of Washington

Publications -  28
Citations -  2493

John C. Angello is an academic researcher from University of Washington. The author has contributed to research in topics: Myocyte & Cell culture. The author has an hindex of 19, co-authored 28 publications receiving 2422 citations.

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Formation of Hyaluronan- and Versican-Rich Pericellular Matrix Is Required for Proliferation and Migration of Vascular Smooth Muscle Cells

TL;DR: Data suggest that organization of HA- and versican-rich pericellular matrices may facilitate migration and mitosis by diminishing cell surface adhesivity and affecting cell shape through steric exclusion and the viscous properties of HA proteoglycan gels.
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SPARC, a secreted protein associated with cellular proliferation, inhibits cell spreading in vitro and exhibits Ca+2-dependent binding to the extracellular matrix.

TL;DR: Exogenous SPARC was associated with profound changes in cell shape, caused rapid, partial detachment of a confluent monolayer, and inhibited spreading of newly plated cells, and it is proposed that SPARC is an extracellular modulator of Ca+2 and cation-sensitive proteins or proteinases, which facilitates changes in cellular shape and disengagement of cells from the extrace cellular matrix.
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EGF and TGF-α stimulate retinal neuroepithelial cell proliferation in vitro

TL;DR: It is reported that two members of another peptide growth factor, epidermal growth factor and transforming growth factor-α, are mitogenic for retinal neuroepithelial cells in primary cultures and provide evidence for the presence of both of these factors in normal developing rat retina.
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In vitro generation of differentiated cardiac myofibers on micropatterned laminin surfaces

TL;DR: Patterned cardiomyocytes displayed a striking, bipolar localization of the junction molecules N-cadherin and connexin43 that ultrastructurally resembled intercalated disks, suggesting that highly patterned cultures could be used in cell biology and physiology studies, which require accurate reproduction of native myocardial architecture.
Journal Article

Reorganization of basement membrane matrices by cellular traction promotes the formation of cellular networks in vitro.

TL;DR: It is found that endothelial cells, fibroblasts, smooth muscle cells, and cells of the murine Leydig cell line TM3 formed networks on basement membrane matrix in much the same fashion, and the mechanochemical properties of extracellular matrices are able to translate the forces of cellular traction into templates that direct the formation of complex cellular patterns.