We demonstrate here the presence of a distinct mature CD4+8- T cell subset in mouse thymus. This subset, termed "Thy0," is delineated by the absence of 3G11 expression from about half of the 6C10-/HSAlow/- fraction of CD4+8- thymic cells. Thy0 is detectable from the neonatal period and largely contributes the Th0-type diverse cytokine production previously reported for the HSAlow/-CD4+ thymic population. Further, cells expressing the T cell receptor V beta 8 gene family are found at increasing frequency in Thy0 with age, comprising 40-60% of Thy0 in adult BALB/c mice. This alteration of V beta 8+ cell frequency is unique to Thy0, since no other CD4+ subset in thymus or spleen shows such V beta 8 overusage. All functional CD4+ T cell subsets, including Thy0, show appropriate V beta clonal deletion associated with endogenous superantigens. Thus, it appears that Thy0 is an intrathymically generated secondary cell subset produced after CD4+ T cell selection.
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1 July 1992
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July 01 1992
Murine thymic CD4+ T cell subsets: a subset (Thy0) that secretes diverse cytokines and overexpresses the V beta 8 T cell receptor gene family.
K Hayakawa,
K Hayakawa
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
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B T Lin,
B T Lin
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
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R R Hardy
R R Hardy
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
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K Hayakawa
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
B T Lin
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
R R Hardy
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1992) 176 (1): 269–274.
Citation
K Hayakawa, B T Lin, R R Hardy; Murine thymic CD4+ T cell subsets: a subset (Thy0) that secretes diverse cytokines and overexpresses the V beta 8 T cell receptor gene family.. J Exp Med 1 July 1992; 176 (1): 269–274. doi: https://doi.org/10.1084/jem.176.1.269
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