The Journal of Experimental Medicine
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© The Rockefeller University Press, 0022-1007/1998/2/609/ $5.00
The Journal of Experimental Medicine, Volume 187, Number 4, February 16, 1998 609-618


Articles

Acquisition of Ly49 Receptor Expression by Developing Natural Killer Cells

Jeffrey R. Dorfman and David H. Raulet

From the Department of Molecular and Cell Biology and the Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720

The formation of the repertoire of mouse natural killer (NK) cell receptors for major histocompatibility complex (MHC) class I molecules was investigated by determining the developmental pattern of Ly49 receptor expression. During the first days after birth, few or no splenic NK cells express Ly49A, Ly49C, Ly49G2, or Ly49I receptors. The proportion of Ly49+ splenic NK cells gradually rises to adult levels during the first 6–8 wk of life. The appearance of appreciable numbers of splenic Ly49+ NK cells coincides with the appearance of NK activity at 3–4 wk. After in vivo transfer, NK cells not expressing specific Ly49 receptors can give rise to NK cells that do, and cells expressing one of these four Ly49 receptors can give rise to cells expressing others. Once initiated, expression of a Ly49 receptor is stable for at least 10 d after in vivo transfer. Hence, initiation of Ly49 receptor expression occurs successively. Interestingly, expression of one of the receptors tested, Ly49A, did not occur after in vivo transfer of Ly49A cells. One possible explanation for these data is that the order of Ly49 receptor expression by NK cells is nonrandom. The results provide a framework for evaluating models of NK cell repertoire formation, and how the repertoire is molded by host class I MHC molecules.


We acknowledge the work of Werner Held in the preliminary experiments that led up to these studies. We also appreciate the assistance of Peter Schow for excellent technical assistance with flow cytometry and production of phycoerythrin and allophycocyanin conjugations of monoclonal antibodies, of B.J. Fowlkes and Russell Vance for critical review of the manuscript, of Joonsoo Kang for helpful discussions, of Andrea Itano for help with the contaminant control experiments, and of Mark Coles and Laura Corral for providing reagents.

This work was supported by National Institutes of Health grant RO1-AI39642 to D.H. Raulet.

Address correspondence to Dr. David H. Raulet, 485 LSA, Department of Molecular and Cell Biology, University of California at Berkeley, Berkeley, CA 94720-3200. Phone: 510-642-9521; Fax: 510-642-1443; E-mail: raulet{at}uclink4.berkeley.edu

J.R. Dorfman's current address is Bldg. 10, Rm. 11N311, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892-1892. E-mail: jdorfman{at}nih.gov


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