白细胞介素21
白细胞介素12
细胞毒性T细胞
Janus激酶3
淋巴因子激活杀伤细胞
生物
NK-92
骨髓
自然杀伤细胞
分子生物学
CD49b
免疫学
体外
生物化学
作者
G C Koo,Florent Dumont,M M Tutt,John Hackett,Vinay Kumar
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:1986-12-01
卷期号:137 (12): 3742-3747
被引量:163
标识
DOI:10.4049/jimmunol.137.12.3742
摘要
The NK-1.1(-) mouse was constructed by weekly injections of monoclonal anti-NK-1.1 antibody from birth through adulthood. Spleen cells from these mice have decreased NK-1.1+ cells and null (Thy-1- and B220-) cells. Their splenic NK activity to YAC targets was low and was not enhanced by IFN-alpha or IFN-beta. Bone marrow (BM) of these NK-1.1(-) mice have normal precursors to NK cells: 1) NK activity could be generated from NK-1.1(-) BM cells cultured in rIL 2 for 5 to 6 days. These cultured BM cells expressed Qa-5, Thy-1, AsGm-1, and NK-1.1 antigens. The precursor cells of these BM cytotoxic cells are NK-1.1-; 2) transfer of BM cells from the NK-1.1(-) mice reconstituted the NK activity of irradiated, NK-depleted recipients. Lymphokine-activated killer cells could also be generated from spleens of these NK-1.1(-) mice. Therefore, the NK-1.1(-) mice were specifically depleted of mature cytotoxic NK cells, but not the NK-1.1- precursors of NK cells. This mouse model is valuable to study ontogeny and physiologic relevance of NK cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI