In Vitro Culturing of PDGFRα-GFP Bright and Dim iReFs

JG Jenna Green
ME Mehari Endale
HA Herbert Auer
AP Anne-Karina T. Perl
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PDGFRα+-GFPbright or -GFPdim iReFs were isolated after 3 days of sham-operated or PNX mice and were sorted using a fluorescence-activated cell sorter, and then cultured for 24 and 72 hours with or without transforming growth factor (TGF)-β1. After this, the proliferation, activation, and differentiation status (Ki67+, CD34, CD29, and α-SMA) were analyzed using a fluorescence-activated cell sorter.

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