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The 3-Deoxy Analogue of ?-GalCer: Disclosing the Role of the 4-Hydroxyl Group for CD1d-Mediated NKT Cell Activation.


ABSTRACT: KRN7000, or ?-GalCer, is a potent agonist for natural killer T (NKT) cells. The 3-hydroxyl group of its phytosphingosine moiety is important for activating NKT cells, whereas its 4-hydroxyl group is perceived to be less crucial. To experimentally determine the role of the 4-hydroxyl group, we synthesized the 3-deoxy analogue of ?-GalCer. It was found that 3-deoxy-?-GalCer induced potent cytokine responses from NKT cells, comparable to those of both ?-GalCer and 4-deoxy-?-GalCer. This result and our docking studies suggest that the effects of an absence of the 3-hydroxyl group are compensated by the presence of a hydroxyl group at the C-4 position. Thus, we conclude that the 4-hydroxyl group of ?-GalCer is as important to the mechanism of action as the 3-hydroxyl group and that the two hydroxyl groups could play individual and cooperative roles in orienting the glycolipid into the proper position in CD1d to be recognized by the T cell receptor of NKT cells.

SUBMITTER: Baek DJ 

PROVIDER: S-EPMC4018141 | biostudies-literature | 2011 Jul

REPOSITORIES: biostudies-literature

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The 3-Deoxy Analogue of α-GalCer: Disclosing the Role of the 4-Hydroxyl Group for CD1d-Mediated NKT Cell Activation.

Baek Dong Jae DJ   Seo Jeong-Hwan JH   Lim Chaemin C   Kim Jae Hyun JH   Chung Doo Hyun DH   Cho Won-Jea WJ   Kang Chang-Yuil CY   Kim Sanghee S  

ACS medicinal chemistry letters 20110516 7


KRN7000, or α-GalCer, is a potent agonist for natural killer T (NKT) cells. The 3-hydroxyl group of its phytosphingosine moiety is important for activating NKT cells, whereas its 4-hydroxyl group is perceived to be less crucial. To experimentally determine the role of the 4-hydroxyl group, we synthesized the 3-deoxy analogue of α-GalCer. It was found that 3-deoxy-α-GalCer induced potent cytokine responses from NKT cells, comparable to those of both α-GalCer and 4-deoxy-α-GalCer. This result and  ...[more]

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