EXPRESSION OF THE W6/32 HLA EPITOPE BY CELLS OF RAT, MOUSE, HUMAN AND OTHER SPECIES - CRITICAL DEPENDENCE ON THE INTERACTION OF SPECIFIC MHC HEAVY-CHAINS WITH HUMAN OR BOVINE BETA-2-MICROGLOBULIN
EXPRESSION OF THE W6/32 HLA EPITOPE BY CELLS OF RAT, MOUSE, HUMAN AND OTHER SPECIES - CRITICAL DEPENDENCE ON THE INTERACTION OF SPECIFIC MHC HEAVY-CHAINS WITH HUMAN OR BOVINE BETA-2-MICROGLOBULIN
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DOI:
10.1002/eji.1830170907
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发表时间:
1987-09-01
影响因子:
5.4
通讯作者:
MACPHERSON, GG
中科院分区:
文献类型:
--
作者:
JEFFERIES, WA;MACPHERSON, GG
The HLA class I epitope W6/32 is conformationally dependent on both heavy chain and .beta.2-microglobulin (.beta.2M). Previously, the W6/32 epitope has been detected in humans and other primates as well as from bovine sources. Two controversial reports suggest the W6/32 epitope is constitutively expressed by either normal or transformed murine cells expressing the Db allele. Here we show that the appearance of the W6/32 epitope in murine cells results from the association of either the Db or Kd gene products with either bovine or human .beta.2M. We use congenic mouse strains and hybrid H-2 class I genes between Db and Kb to map the W6/32 epitope to particular amino acid residues in the .alpha.2 domain. Subsequently, we show that .beta.2M exchange is not confined to murine or human cells in vitro but can be detected after .beta.2M injection into a mouse. The data presented suggests that .beta.2M exchange takes place at the cell surface under physiological conditions and indicates that MHC class I heavy chains are in an equilibrium between the bound and unbound form of .beta.2M.