A glycolipid on the surface of mouse natural killer cells
✍ Scribed by Masataka Kasai; Masao Iwamod; Yoshitaka Nagai; Ko Okumura; Tomio Tada
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 614 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0014-2980
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✦ Synopsis
Abstract
Cytotoxic treatment with rabbit antiserum raised against purified glycosphingolipid “asialo GM1” was capable of eliminating natural killer (NK) activity of spleen cells from different inbred mouse strains including CBA/J, C57BL/6, BALB/c, AKR, and athymic nude mice. The anti‐asialo GM 1 antiserum showed little cross‐reactivity with structurally related glycolipids, e.g. GM 1, GD 1 b and asialo GM 2 in the microflocculation test. The specific reactivity of this antiserum with NK cells was confirmed by the quantitative absorption of anti‐NK activity with graded amounts of asialo GM 1 but not with other glycosphingolipids. The absorption of anti‐brain‐associated T cell antigen (anti‐BAT) with asialo GM 1 also effectively diminished its anti‐NK activity, leaving the ability to kill T cells intact. This suggests that the antibody to asialo GM 1 is responsible for the anti‐NK activity contained in the anti‐BAT antiserum. In contrast to the extreme sensitivity of NK cells to anti‐asialo GM 1, alloreactive cytotoxic T killer cells generated in the mixed lymphocyte culture were not killed by anti‐asialo GM 1 and complement. These results indicate that asialo GM 1 is expressed on mouse NK cells in a high concentration.
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The possible effect of IL-2, a,P-IFN and poly I:C (an IFN inducer) administration on the generation of NK cells of LI and BM-reconstituted animals was investigated. B6D2FI mice were LI (9.5 Gy) by total-body irradiation and reconstituted by i.v. injection of different doses (ranging from lo6 to 2 x