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. Author manuscript; available in PMC: 2018 Mar 30.
Published in final edited form as: J Tissue Eng Regen Med. 2017 Apr 9;12(1):e541–e549. doi: 10.1002/term.2324

Figure 1.

Figure 1

Experimental overview. hASCs were expanded in monolayer in vitro and then collected for cell pellet formation via centrifugation or alginate bead formation. Samples were cultured in chondrogenic induction medium for 4 weeks, encapsulated in agarose carriers and maintained overnight in chondrogenic medium prior to subcutaneous implantation in the cervical region of immune-compromised mice. After 8 weeks in vivo, samples were removed, scanned by μCT and processed for histological evaluation.