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HIV enhances substance P expression in human immune cells
Author(s) -
Ho Wen-Zhe,
Lai Jian-Ping,
Li Yuan,
Douglas Steven D.
Publication year - 2002
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.01-0655fje
Subject(s) - immune system , reverse transcriptase , biology , virus , cell culture , monocyte , virology , recombinant dna , ex vivo , microbiology and biotechnology , lymphocyte , in vivo , gene expression , viral replication , messenger rna , immunology , polymerase chain reaction , gene , biochemistry , genetics
Substance P (SP), a potent modulator of neuroimmunoregulation, is expressed in human immune cells. We observed elevated plasma SP levels in HIV‐infected men compared with uninfected subjects. In the present study, we investigated the possible cellular source of the increased SP level caused by HIV infection. Using real‐time reverse transcriptase‐polymerase chain reaction, we demonstrated that monocyte‐derived macrophages (MDM) and lymphocytes from both placental cord blood and adult peripheral blood expressed SP mRNA, which was significantly increased by HIV infection. HIV‐induced SP expression was positively related to virus replication in the infected MDM. Purified recombinant HIV envelope glycoprotein 120 (gp120) derived from both the macrophage‐tropic strain (MN) and the T lymphocyte‐tropic strain (IIIB), when added to MDM cultures, enhanced SP mRNA expression. The gp120‐induced SP expression was abrogated by pretreating the cells with soluble CD 4. Furthermore, the activation of HIV in the latently infected promonocytic cell line (U1) and T‐cell line (ACH‐2) up‐regulated SP mRNA expression. These data support the hypothesis that interaction of HIV and SP may have significant in vivo relevance to the immunopathogenesis of HIV infection and AIDS.