| First Author | Stotesbury C | Year | 2020 |
| Journal | J Immunol | Volume | 204 |
| Issue | 6 | Pages | 1582-1591 |
| PubMed ID | 32015010 | Mgi Jnum | J:287109 |
| Mgi Id | MGI:6406191 | Doi | 10.4049/jimmunol.1900927 |
| Citation | Stotesbury C, et al. (2020) alpha2beta1 Integrin Is Required for Optimal NK Cell Proliferation during Viral Infection but Not for Acquisition of Effector Functions or NK Cell-Mediated Virus Control. J Immunol 204(6):1582-1591 |
| abstractText | NK cells play an important role in antiviral resistance. The integrin alpha2, which dimerizes with integrin beta1, distinguishes NK cells from innate lymphoid cells 1 and other leukocytes. Despite its use as an NK cell marker, little is known about the role of alpha2beta1 in NK cell biology. In this study, we show that in mice alpha2beta1 deficiency does not alter the balance of NK cell/ innate lymphoid cell 1 generation and slightly decreases the number of NK cells in the bone marrow and spleen without affecting NK cell maturation. NK cells deficient in alpha2beta1 had no impairment at entering or distributing within the draining lymph node of ectromelia virus (ECTV)-infected mice or at becoming effectors but proliferated poorly in response to ECTV and did not increase in numbers following infection with mouse CMV (MCMV). Still, alpha2beta1-deficient NK cells efficiently protected from lethal mousepox and controlled MCMV titers in the spleen. Thus, alpha2beta1 is required for optimal NK cell proliferation but is dispensable for protection against ECTV and MCMV, two well-established models of viral infection in which NK cells are known to be important. |
