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Alan C. Rapraeger

Researcher at University of Wisconsin-Madison

Publications -  90
Citations -  10637

Alan C. Rapraeger is an academic researcher from University of Wisconsin-Madison. The author has contributed to research in topics: Heparan sulfate & Syndecan 1. The author has an hindex of 55, co-authored 86 publications receiving 10224 citations. Previous affiliations of Alan C. Rapraeger include Stanford University.

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Requirement of heparan sulfate for bFGF-mediated fibroblast growth and myoblast differentiation.

TL;DR: Prevention of binding between cell surface heparan sulfate and bFGF substantially reduces binding of fibroblast growth factor to its cell-surface receptors, blocks the ability of bF GF to support the growth of Swiss 3T3 fibroblasts, and induces terminal differentiation of MM14 skeletal muscle cells, which is normally repressed by fibro Blast growth factor.
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Activating and inhibitory heparin sequences for FGF-2 (basic FGF). Distinct requirements for FGF-1, FGF-2, and FGF-4.

TL;DR: It is concluded that specific saccharide sequences within heparan sulfate glycosaminoglycan chains favor the signaling by distinct members of the FGF family.
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Syndecan-3 and syndecan-4 specifically mark skeletal muscle satellite cells and are implicated in satellite cell maintenance and muscle regeneration.

TL;DR: Examination of the expression of syndecans 1-4 in embryonic, fetal, postnatal, and adult muscle tissue, as well as on primary adult muscle fiber cultures, suggests that syndecan-3 and syndECan-4 may play important regulatory roles in satellite cell maintenance, activation, proliferation, and differentiation during skeletal muscle regeneration.
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Cell surface proteoglycan associates with the cytoskeleton at the basolateral cell surface of mouse mammary epithelial cells.

TL;DR: It is suggested that the proteoglycan, initially present on the entire surface and free in the plane of the membrane, becomes sequestered at the basolateral cell surface and bound to the actin-rich cytoskeleton as the cells become polarized in vitro.
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Essential and separable roles for Syndecan-3 and Syndecan-4 in skeletal muscle development and regeneration.

TL;DR: While there are fewer apparent defects in syndecan-4(-/-) muscle, explanted satellite cells are deficient in activation, proliferation, MyoD expression, myotube fusion, and differentiation, suggesting a unique requirement for syndecans-4 in satellite cell function.