South African Mutations of the CCR5 Coreceptor for HIV Modify Interaction With Chemokines and HIV Envelope Protein

作者：Folefoc Asongna T; Fromme Bernhard J; Katz Arieh A; Flanagan Colleen A^*

来源：JAIDS: Journal of Acquired Immune Deficiency Syndromes , 2010, 54(4): 352-359.

DOI：10.1097/QAI.0b013e3181e0c7b2

• CCR5 coreceptor mutants
• CCR5 expression
• Env-directed fusion

The CCR5 chemokine receptor is the major coreceptor for HIV-1 and the receptor for CC-chemokines, MIP-1 alpha, MIP-1 beta, and regulated upon activation normal T-cell-expressed and secreted. Individuals, who are homozygous for the nonfunctional CCR5 Delta 32 allele, are largely resistant to HIV-1 infection. Four unique mutations that affect the amino acid sequence of CCR5 have been identified in South Africa. We have assessed the effect of these mutations on CCR5 interactions with chemokines and HIV Envelope protein. The Leu(107)Phe mutation did not affect CCR5 expression, chemokine binding, intracellular signaling, or interaction with Envelope. The Arg(225)Gln mutant was similar to wild-type CCR5, but ligand-independent intracellular signaling suggests that it is partially constitutively active. The Asp(2)Val mutation decreased chemokine-binding affinity, chemokine-stimulated intracellular signaling, and receptor expression. It also decreased HIV Envelope-mediated cell fusion. The Arg(225)Stop mutant showed no measurable chemokine binding or signaling and no measurable expression of CCR5 at the cell surface or within the cell. Consistent with lack of cell surface expression, it did not support envelope-mediated cell fusion. These results show that South African CCR5 variants have a range of phenotypes in vitro that may reflect altered chemokine responses and susceptibility to HIV infection in individuals who carry these alleles.

• 出版日期2010-8-1