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. Author manuscript; available in PMC: 2009 May 7.
Published in final edited form as: Tissue Eng Part A. 2009 Feb;15(2):243–254. doi: 10.1089/ten.tea.2008.0067

Figure 1. MSC interactions with HA.

Figure 1

Immunofluorescence staining of CD44 (green) with nuclear counterstain (blue) of MSCs cultured in 2D on glass coverslips (scale bar = 100μm) (A), flow cytometry staining for CD44 (yellow) compared to unstained (black) population of MSCs prior to encapsulation (B), and live (green)/dead (red) image of MSCs encapsulated in MeHA hydrogel 6 hours after photopolymerization (scale bar = 200μm) (C).