In vivo commitment and functional tissue regeneration using human embryonic stem cell-derived mesenchymal cells
Author(s) -
Nathaniel S. Hwang,
Shyni Varghese,
H. Janice Lee,
Zijun Zhang,
Zhaohui Ye,
Jongwoo Bae,
Linzhao Cheng,
Jennifer H. Elisseeff
Publication year - 2008
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0809680106
Subject(s) - mesenchymal stem cell , embryonic stem cell , microbiology and biotechnology , chondrogenesis , clinical uses of mesenchymal stem cells , regenerative medicine , stem cell transplantation for articular cartilage repair , tissue engineering , cartilage , stem cell , biology , regeneration (biology) , cellular differentiation , adult stem cell , immunology , anatomy , biochemistry , gene , genetics
Development of clinically relevant regenerative medicine therapies using human embryonic stem cells (hESCs) requires production of a simple and readily expandable cell population that can be directed to form functional 3D tissue in an in vivo environment. We describe an efficient derivation method and characterization of mesenchymal stem cells (MSCs) from hESCs (hESCd-MSCs) that have multilineage differentiation potential and are capable of producing fat, cartilage, and bone in vitro. Furthermore, we highlight their in vivo survival and commitment to the chondrogenic lineage in a microenvironment comprising chondrocyte-secreted morphogenetic factors and hydrogels. Normal cartilage architecture was established in rat osteochondral defects after treatment with chondrogenically-committed hESCd-MSCs. In view of the limited available cell sources for tissue engineering applications, these embryonic-derived cells show significant potential in musculoskeletal tissue regeneration applications.
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