Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1987 Jul 1;166(1):12-32.
doi: 10.1084/jem.166.1.12.

Molecular, cellular, and functional properties of bone marrow T lymphocyte progenitor clones

Molecular, cellular, and functional properties of bone marrow T lymphocyte progenitor clones

R Palacios et al. J Exp Med. .

Erratum in

  • J Exp Med 1988 Jun 1;167(6):2023

Abstract

The continuous proliferating bone marrow clones C4-77, C4-86, and C4-95 express low levels of Thy-1 and Ly-1 surface antigens, but no detectable surface antigens normally present on thymocytes, peripheral mature T lymphocytes, cells of the B lymphocyte or myeloid lineages. They contain the T cell antigen receptor genes alpha, beta, and the T cell-specific gene gamma in the germline configuration, and they express functional receptors for IL-3 and nonfunctional receptors for IL-2. The C4 clones are able to home and undergo differentiation in the thymus of sublethally irradiated mice and give rise in vivo to phenotypically and functionally mature peripheral T lymphocytes displaying several antigen specificities. In vitro 5-Azacytidine induces the C4 clones to express Lyt-2 and L3T4 T cell differentiation antigens, and renders them amenable to be switched from IL-3 to IL-2 dependence. However, the C4 clones seem incapable of giving rise to B lymphocytes either in vivo or in vitro. They self-renew in vitro in the presence of IL-3 every 12-14 h. We conclude that the C4 clones represent cells at the earliest stage of T cell development, i.e., Pro-T lymphocytes.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Cell Physiol. 1967 Apr;69(2):177-84 - PubMed
    1. J Exp Med. 1967 Oct 1;126(4):715-26 - PubMed
    1. J Exp Med. 1977 Jun 1;145(6):1567-79 - PubMed
    1. J Natl Cancer Inst. 1980 Aug;65(2):241-7 - PubMed
    1. Immunogenetics. 1982 Mar;15(3):299-312 - PubMed

Publication types