EFFECTS OF COCAINE ON HPA AXIS IN MACAQUE MOTHER & FETUS
EFFECTS OF COCAINE ON HPA AXIS IN MACAQUE MOTHER & FETUS
批准号:
6312845
负责人:
OLINE K RXNNEKLEIV
金额:
$5.84万
依托单位国家:
美国
项目类别:
财政年份:
1978
资助国家:
美国
项目状态:
已结题
起止时间:
1978-05-01 至 2004-04-30
中文摘要
点击翻译按钮获取中文摘要
英文摘要
While HIV-1 V3 is known to be important in determining viral cell
tropism and coreceptor usage, little is known about the role of SIV
V3. The objective of this study is to investigate the significance of
SIV V3 for viral cell tropism and coreceptor usage. In this study, we
have used three molecularly cloned SIV with distinct cell tropisms,
coreceptor usages and the V3 sequences T cell-tropic SIVmacEvT3 using
CXCR4 as a coreceptor, human T cell line-tropic SIVmac239 using CCR5,
and macrophage-tropic SIVmacEvM3 using CCR5. We have exchanged V3
sequences of each cloned SIV with those of other clones to construct
V3 recombinant viruses. Our data obtained from V3 recombinants have
shown that the cell tropism and coreceptor usage of each SIV are
primarily determined by the V3 sequences. Site-specific mutagenesis
studies have further demonstrated that the charge of the amino acids
within SIV V3 sequences plays an important role in determining the
viral cell tropisms an d corecep tor usage. This suggests that the
charge of V3 sequences of SIV, like those of HIV-1, contributes to the
formation of coreceptor binding sites in gp120, which may contain the
V3 region or be conformationally influenced by it. Interestingly,
some of the constructed mutant viruses could use both CXCR4 and CCR5
for virus entry, similar to dual-tropic HIV-1. Since EvT3 using
CXCR4, but not 239 using CCR5, induces rapid and severe CD4+ T cell
depletion in rhesus macaques, it will be important to examine the
pathogenic potential of dual-tropic SIV in vivo. Further studies with
the rhesus macaque model using coreceptor-specific SIV clones that
utilize CXCR4, CCR5 or CXCR4 and CCR5 will provide important
information to better understand the mechanisms and significance of
HIV-1 coreceptor changes from CCR5 to CXCR4 in AIDS patients. FUNDING
NIH RR00163 (Project 2) PUBLICATIONS Martin K, Hagen S, Kodama T.
Genetic determinants of SIV CXCR4 usage the role of V1 and V3
sequences. In 16th Annual Symposium on Nonhuman Primate Models for
AIDS (held in Atlanta, GA, October 7-10, 1998) (abstract 3).
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
EFFECTS OF COCAINE IN FETAL MONKEY BRAIN
-
批准号:6592287
-
项目类别:
-
资助金额:$11.11万
-
财政年份:2002
-
负责人:OLINE K RXNNEKLEIV
-
依托单位:
EFFECTS OF COCAINE IN FETAL MONKEY BRAIN
-
批准号:6453663
-
项目类别:
-
资助金额:$11.11万
-
财政年份:2001
-
负责人:OLINE K RXNNEKLEIV
-
依托单位:
EFFECTS OF COCAINE IN FETAL MONKEY BRAIN
-
批准号:6116109
-
项目类别:
-
资助金额:$8.93万
-
财政年份:1999
-
负责人:OLINE K RXNNEKLEIV
-
依托单位:
EFFECTS OF COCAINE IN FETAL MONKEY BRAIN
-
批准号:6312844
-
项目类别:
-
资助金额:$5.84万
-
财政年份:1978
-
负责人:OLINE K RXNNEKLEIV
-
依托单位:
海外基金