Gab3 is required for IL-2- and IL-15-induced NK cell expansion and limits trophoblast invasion during pregnancy

• Published in: Science immunology Vol. 4; no. 38
• Main Authors: Sliz, Anna, Locker, Kathryn C S, Lampe, Kristin, Godarova, Alzbeta, Plas, David R, Janssen, Edith M, Jones, Helen, Herr, Andrew B, Hoebe, Kasper
• Format: Journal Article
• Language: English
• Published: United States 02.08.2019
• Subjects: Adaptor Proteins, Signal Transducing - deficiency; Adaptor Proteins, Signal Transducing - immunology; Animals; Female; Interleukin-15 - immunology; Interleukin-2 - immunology; Killer Cells, Natural - immunology; Mice; Mice, Knockout; Pregnancy; Trophoblasts - immunology
• ISSN: 2470-9468
• DOI: 10.1126/sciimmunol.aav3866

The scaffolding protein Grb2-associated binding protein 3 (Gab3) is a member of the Gab family, whose functions have remained elusive. Here, we identify Gab3 as a key determinant of peripheral NK cell expansion. Loss of Gab3 resulted in impaired IL-2 and IL-15-induced NK cell priming and expansion due to a selective impairment in MAPK signaling but not STAT5 signaling. In vivo, we found that Gab3 is required for recognition and elimination of "missing-self" and tumor targets. Unexpectedly, our studies also revealed that Gab3 plays an important role during pregnancy. Gab3-deficient mice exhibited impaired uterine NK cell expansion associated with abnormal spiral artery remodeling and increased trophoblast invasion in the decidua basalis. This coincided with stillbirth, retained placenta, maternal hemorrhage, and undelivered fetoplacental units at term. Thus, Gab3 is a key component required for cytokine-mediated NK cell priming and expansion that is essential for antitumor responses and limits trophoblast cell invasion during pregnancy.