Natural killer (NK) cells mediate defense against early murine cytomegalovirus (MCMV) infections in liver. The chemokine, macrophage inflammatory protein 1α (MIP-1α), can promote inflammatory responses. Our studies evaluated contributions of NK cells to early MCMV-induced liver inflammation and MIP-1α requirements for inflammation and delivery of antiviral defenses. NK cells were shown to be responsible for focal inflammation, and to be induced to migrate at high levels, in MCMV-infected livers. MIP-1α gene expression was elevated at coinciding times, and mice deficient in MIP-1α function were dramatically inhibited in both inflammatory and protective liver responses. The results precisely define MIP-1α–dependent steps required to achieve NK cell inflammation during, and mechanisms promoting defense against, viral infections in tissues.
Early Murine Cytomegalovirus (MCMV) Infection Induces Liver Natural Killer (NK) Cell Inflammation and Protection Through Macrophage Inflammatory Protein 1α (MIP-1α)–dependent Pathways
The study was supported by National Institutes of Health grant CA-41268.
Correspondence should be addressed to Christine A. Biron, Department of Molecular Microbiology and Immunology, Division of Biology and Medicine, Brown University, Box G-B269, Providence, RI 02912. Phone: 401-863-2921; FAX: 401-863-9045; E-mail: [email protected]
Abbreviations used in this paper: AGM1, asialo ganglio-N-tetraoglyceramide; CMV, cytomegalovirus; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; H&E, hematoxylin and eosin; MCMV, murine CMV; MIP-1α, macrophage inflammatory protein 1α; mRNA, messenger RNA; RAG, recombination activation gene.
Thais P. Salazar-Mather, Jordan S. Orange, Christine A. Biron; Early Murine Cytomegalovirus (MCMV) Infection Induces Liver Natural Killer (NK) Cell Inflammation and Protection Through Macrophage Inflammatory Protein 1α (MIP-1α)–dependent Pathways . J Exp Med 5 January 1998; 187 (1): 1–14. doi: https://doi.org/10.1084/jem.187.1.1
Download citation file:
Sign in
Client Account
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement