Broad usage spectrum of G protein-coupled receptors as coreceptors by primary isolates of HIV
Objective: HIV-1 can use various G protein-coupled receptors (GPCRs) in addition to CCR5 and CXCR4 as coreceptors;however, this type of HIV-1 infection has hardly been detected in vivo. The objective of this study was to elucidate the spectrum of GPCR usage by HIV-1 populations in vivo. Design: CD4-...
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th-cmuir.6653943832-596392018-09-10T03:22:25Z Broad usage spectrum of G protein-coupled receptors as coreceptors by primary isolates of HIV Nobuaki Shimizu Atsushi Tanaka Atsushi Oue Takahisa Mori Takahiro Ohtsuki Chatchawann Apichartpiyakul Hideki Uchiumi Yoshihisa Nojima Hiroo Hoshino Immunology and Microbiology Medicine Objective: HIV-1 can use various G protein-coupled receptors (GPCRs) in addition to CCR5 and CXCR4 as coreceptors;however, this type of HIV-1 infection has hardly been detected in vivo. The objective of this study was to elucidate the spectrum of GPCR usage by HIV-1 populations in vivo. Design: CD4-expressing glioma cell line, NP-2/CD4, becomes highly susceptible to HIV-1 when the cells express GPCRs with coreceptor activities. This cell system was advantageous for detecting the inefficient use of GPCRs by HIV-1. Methods: We developed NP-2/CD4/GPCR cells that express each of 23 GPCRs: 21 chemokine receptors (CCR1, CCR2b, CCR3, CCR4, CCR5, CCR6, CCR7, CCR8, CCR9B, CCR10, CCR11, CXCR1, CXCR2, CXCR3, CXCR4, CXCR5, CXCR6, CX3CR1, XCR1, D6, and DARC) and two other GPCRs (a formylpeptide receptor, FPRL1, and an orphan GPCR, GPR1). NP-2/CD4/GPCR cells were directly cocultured with HIV-1-positive peripheral blood lymphocytes and HIV-1 infection was detected. Results: Primary HIV-1 isolates were obtained from NP-2/CD4/GPCR cells expressing CCR5, CXCR4, FPRL1, or GPR1 cocultured with 11 of 17 peripheral blood lymphocytes. Surprisingly, these isolates showed extremely expanded GPCR usage, such as CCR1, CCR3, CCR5, CCR8, CXCR4, D6, FPRL1, and GPR1 as coreceptors. We found that CCR9B, CCR10, and XCR1 also work as novel HIV-1 coreceptors. Conclusion: FPRL1 and GPR1 have the potential to work as significant HIV-1 cor- eceptors in vivo next to CCR5 and CXCR4. HIV-1 populations that can use various GPCRs as coreceptors are already circulating in vivo, even in the early stage of HIV-1 infection. © 2009 Wolters Kluwer Health | Lippincott Williams & Wilkins. 2018-09-10T03:18:43Z 2018-09-10T03:18:43Z 2009-04-27 Journal 14735571 02699370 2-s2.0-67649668892 10.1097/QAD.0b013e328326cc0d https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67649668892&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/59639 |
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Immunology and Microbiology Medicine Nobuaki Shimizu Atsushi Tanaka Atsushi Oue Takahisa Mori Takahiro Ohtsuki Chatchawann Apichartpiyakul Hideki Uchiumi Yoshihisa Nojima Hiroo Hoshino Broad usage spectrum of G protein-coupled receptors as coreceptors by primary isolates of HIV |
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Objective: HIV-1 can use various G protein-coupled receptors (GPCRs) in addition to CCR5 and CXCR4 as coreceptors;however, this type of HIV-1 infection has hardly been detected in vivo. The objective of this study was to elucidate the spectrum of GPCR usage by HIV-1 populations in vivo. Design: CD4-expressing glioma cell line, NP-2/CD4, becomes highly susceptible to HIV-1 when the cells express GPCRs with coreceptor activities. This cell system was advantageous for detecting the inefficient use of GPCRs by HIV-1. Methods: We developed NP-2/CD4/GPCR cells that express each of 23 GPCRs: 21 chemokine receptors (CCR1, CCR2b, CCR3, CCR4, CCR5, CCR6, CCR7, CCR8, CCR9B, CCR10, CCR11, CXCR1, CXCR2, CXCR3, CXCR4, CXCR5, CXCR6, CX3CR1, XCR1, D6, and DARC) and two other GPCRs (a formylpeptide receptor, FPRL1, and an orphan GPCR, GPR1). NP-2/CD4/GPCR cells were directly cocultured with HIV-1-positive peripheral blood lymphocytes and HIV-1 infection was detected. Results: Primary HIV-1 isolates were obtained from NP-2/CD4/GPCR cells expressing CCR5, CXCR4, FPRL1, or GPR1 cocultured with 11 of 17 peripheral blood lymphocytes. Surprisingly, these isolates showed extremely expanded GPCR usage, such as CCR1, CCR3, CCR5, CCR8, CXCR4, D6, FPRL1, and GPR1 as coreceptors. We found that CCR9B, CCR10, and XCR1 also work as novel HIV-1 coreceptors. Conclusion: FPRL1 and GPR1 have the potential to work as significant HIV-1 cor- eceptors in vivo next to CCR5 and CXCR4. HIV-1 populations that can use various GPCRs as coreceptors are already circulating in vivo, even in the early stage of HIV-1 infection. © 2009 Wolters Kluwer Health | Lippincott Williams & Wilkins. |
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Journal |
author |
Nobuaki Shimizu Atsushi Tanaka Atsushi Oue Takahisa Mori Takahiro Ohtsuki Chatchawann Apichartpiyakul Hideki Uchiumi Yoshihisa Nojima Hiroo Hoshino |
author_facet |
Nobuaki Shimizu Atsushi Tanaka Atsushi Oue Takahisa Mori Takahiro Ohtsuki Chatchawann Apichartpiyakul Hideki Uchiumi Yoshihisa Nojima Hiroo Hoshino |
author_sort |
Nobuaki Shimizu |
title |
Broad usage spectrum of G protein-coupled receptors as coreceptors by primary isolates of HIV |
title_short |
Broad usage spectrum of G protein-coupled receptors as coreceptors by primary isolates of HIV |
title_full |
Broad usage spectrum of G protein-coupled receptors as coreceptors by primary isolates of HIV |
title_fullStr |
Broad usage spectrum of G protein-coupled receptors as coreceptors by primary isolates of HIV |
title_full_unstemmed |
Broad usage spectrum of G protein-coupled receptors as coreceptors by primary isolates of HIV |
title_sort |
broad usage spectrum of g protein-coupled receptors as coreceptors by primary isolates of hiv |
publishDate |
2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67649668892&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/59639 |
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1681425288577155072 |