淋巴细胞生成
祖细胞
类有机物
细胞生物学
干细胞
离体
生物
T细胞
骨髓
川地34
间质细胞
造血
免疫学
分子生物学
癌症研究
免疫系统
体外
生物化学
作者
Mark C. Poznansky,Richard H. Evans,Russell B. Foxall,Ivona T. Olszak,Anita H. Piascik,Kelly E. Hartman,Christian Brander,Thomas Meyer,Mark Pykett,Karissa T. Chabner,Spyros A. Kalams,Michael Rosenzweig,David T. Scadden
摘要
Biocompatible inorganic matrices have been used to enhance bone repair by integrating with endogenous bone architecture. Hypothesizing that a three-dimensional framework might support reconstruction of other tissues as well, we assessed the capacity of a tantalum-coated carbon matrix to support reconstitution of functioning thymic tissue. We engineered a thymic organoid by seeding matrices with murine thymic stroma. Co-culture of human bone marrow-derived hematopoietic progenitor cells within this xenogeneic environment generated mature functional T cells within 14 days. The proportionate T-cell yield from this system was highly reproducible, generating over 70% CD3+ T cells from either AC133+ or CD34+ progenitor cells. Cultured T cells expressed a high level of T-cell receptor excision circles (TREC), demonstrating de novo T lymphopoiesis, and function of fully mature T cells. This system not only facilitates analysis of the T-lymphopoietic potential of progenitor cell populations; it also permits ex vivo genesis of T cells for possible applications in treatment of immunodeficiency.
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