MicroRNA‐146a deficiency enhances host protection against murine cytomegalovirus

Natural killer (NK) cells are innate lymphoid cells that protect a host from viral infections and malignancies. MicroRNA-146a (miR-146a) is an important regulator of immune function that is highly expressed in NK cells and is further upregulated during murine cytomegalovirus (MCMV) infection. Here we utilized mice with a global targeted deletion of miR-146a to understand its impact on the innate immune responses to MCMV infection. MiR-146a<sup>-/-</sup> mice were protected from lethal MCMV infection, which was intrinsic to the hematopoietic compartment based on bone marrow chimera experiments. NK cell depletion abrogated this protection, implicating NK cells as critical for the miR-146a<sup>-/-</sup> protection from MCMV. Surprisingly, NK cells from miR-146a-deficient mice were largely similar to control NK cells with respect to development, maturation, trafficking, and effector functions. However, miR-146a<sup>-/-</sup> mice had increased NK cell numbers and frequency of the most mature Stage IV (CD27<sup>-</sup>CD11b<sup>+</sup>) NK cells in the liver at baseline, enhanced STAT1 phosphorylation, and increased selective expansion of Ly49H<sup>+</sup> NK cells and T cells during MCMV infection. This study demonstrates a critical role for miR-146a in the host response to MCMV, arising from mechanisms that include increased NK cell numbers and early T-cell expansion.

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Publication Details

Journal
European Journal of Immunology
Published
2024-09-09
DOI
https://doi.org/10.1002/eji.202451173
Citations
2
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.48

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article

MicroRNA‐146a deficiency enhances host protection against murine cytomegalovirus

Jeanette T. Pingel, Pamela Wong, Lynne Marsala, Todd A. Fehniger et al.
2 citations
European Journal of Immunology
Immune Cell Function and Interaction
0.48
article

MicroRNA‐146a deficiency enhances host protection against murine cytomegalovirus

Jeanette T. Pingel, Pamela Wong, Lynne Marsala, Todd A. Fehniger, Anthony R. French, Carly C. Neal, Melissa M. Berrien‐Elliott, Lily Chang, Tony Yao, Jeffrey Leong, Julia A. Wagner, Kimberly Hwang, Jennifer Tran, Megan A. Cooper, Timothy Schappe, Molly P. Keppel, Leslie A. Fogel, Hyogon Sohn, Ryan P. Sullivan, Catherine R. Keppel, Celia C. Cubitt, Stephanie Schneider, Allison Burdi
article en
2 citations

Abstract

Natural killer (NK) cells are innate lymphoid cells that protect a host from viral infections and malignancies. MicroRNA-146a (miR-146a) is an important regulator of immune function that is highly expressed in NK cells and is further upregulated during murine cytomegalovirus (MCMV) infection. Here we utilized mice with a global targeted deletion of miR-146a to understand its impact on the innate immune responses to MCMV infection. MiR-146a<sup>-/-</sup> mice were protected from lethal MCMV infection, which was intrinsic to the hematopoietic compartment based on bone marrow chimera experiments. NK cell depletion abrogated this protection, implicating NK cells as critical for the miR-146a<sup>-/-</sup> protection from MCMV. Surprisingly, NK cells from miR-146a-deficient mice were largely similar to control NK cells with respect to development, maturation, trafficking, and effector functions. However, miR-146a<sup>-/-</sup> mice had increased NK cell numbers and frequency of the most mature Stage IV (CD27<sup>-</sup>CD11b<sup>+</sup>) NK cells in the liver at baseline, enhanced STAT1 phosphorylation, and increased selective expansion of Ly49H<sup>+</sup> NK cells and T cells during MCMV infection. This study demonstrates a critical role for miR-146a in the host response to MCMV, arising from mechanisms that include increased NK cell numbers and early T-cell expansion.

European Journal of ImmunologyVol. 54(12)
Washington University in St. Louis (US)
Howard Hughes Medical Institute, Lymphoma Research Foundation, V Foundation for Cancer Research, Leukemia and Lymphoma Society, Children's Discovery Institute, Alvin J. Siteman Cancer Center, Paula and Rodger Riney Foundation, National Institutes of Health, National Cancer Institute
Openalex Percentile: Top 35%
Immune Cell Function and Interaction
0.48
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