Identification of a Novel Developmental Stage Marking Lineage Commitment of Progenitor Thymocytes

Author:

Carlyle James R.1,Michie Alison M.1,Furlonger Caren1,Nakano Toru1,Lenardo Michael J.1,Paige Christopher J.11,Zúñiga-Pflücker Juan Carlos1

Affiliation:

1. From the Department of Immunology, University of Toronto, Toronto, Ontario M5S 1A8, Canada; The Wellesley Hospital Research Institute, Toronto, Ontario M4Y 1J3, Canada; Department of Molecular Cell Biology, Research Institute for Microbial Diseases, Osaka University, Yamada-Oka 3-1, Suita, Osaka 565, Japan; and the Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, N

Abstract

Bipotent progenitors for T and natural killer (NK) lymphocytes are thought to exist among early precursor thymocytes. The identification and functional properties of such a progenitor population remain undefined. We report the identification of a novel developmental stage during fetal thymic ontogeny that delineates a population of T/NK-committed progenitors (NK1.1+/CD117+/CD44+/CD25−). Thymocytes at this stage in development are phenotypically and functionally distinguishable from the pool of multipotent lymphoid-restricted (B, T, and NK) precursor thymocytes. Exposure of multipotent precursor thymocytes or fetal liver– derived hematopoietic progenitors to thymic stroma induces differentiation to the bipotent developmental stage. Continued exposure to a thymic microenvironment results in predominant commitment to the T cell lineage, whereas coculture with a bone marrow–derived stromal cell line results in the generation of mature NK cells. Thus, the restriction point to T and NK lymphocyte destinies from a multipotent progenitor stage is marked by a thymus-induced differentiation step.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

Reference45 articles.

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