Affiliation:
1. Immunologie‐oncologie, Centre de Recherche de l'Hôpital Maisonneuve‐Rosemont Montréal QC Canada
2. Département de Microbiologie, Infectiologie et Immunologie Université de Montréal Montréal QC Canada
3. Département de Médecine Université de Montréal Montréal QC Canada
Abstract
AbstractNK cells are innate immune cells that target infected and tumor cells. Mature NK (mNK) cells undergo functional maturation characterized by four distinct stages, during which they acquire their cytotoxic properties. mNK cells from non‐obese diabetic (NOD) mice exhibit a defect in functional maturation and have impaired cytotoxic functions. Hence, we tested whether the impaired cytotoxic function observed in mNK cells from NOD mice can be explained by their defect in functional maturation. By comparing the function of mNK cells from B6, B6g7 and NOD mice, we show that the expression of granzyme B is severely impaired in mNK cells from NOD mice, agreeing with their inability to control tumor growth in vivo. The low level of granzyme B expression in mNK cells from NOD mice is found at all stages of functional maturation and is therefore independent of their functional maturation defect. Consequently, this study demonstrates that phenotypic functional maturation of mNK cells can be uncoupled from the acquisition of cytotoxic functions.
Funder
Canadian Institutes of Health Research
Cancer Research Society
Subject
Cell Biology,Immunology,Immunology and Allergy