HIV-1-derived single-stranded RNA acts as activator of human neutrophils
Neutrophils are key effector cells of the innate immune system and are involved in the host defense against invading pathogens such as viruses. Recently, it was reported that HIV-1–neutrophil interaction triggers neutrophil activation and promotes expression of Toll-like receptors (TLRs). Here, we a...
- Autores:
-
Giraldo, D. M.
Hernández López, Juan Carlos
Urcuqui Inchima, S.
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2023
- Institución:
- Universidad Cooperativa de Colombia
- Repositorio:
- Repositorio UCC
- Idioma:
- OAI Identifier:
- oai:repository.ucc.edu.co:20.500.12494/49546
- Acceso en línea:
- https://doi.org/10.1007/s12026-016-8876-9
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84990877450&doi=10.1007%2fs12026-016-8876-9&partnerID=40&md5=3987b423e49a8df3a9e8b2d643d91c1d
https://hdl.handle.net/20.500.12494/49546
- Palabra clave:
- ADULT
ARTICLE
CD11B ANTIGEN
CYTOKINE RELEASE
FEMALE
HUMAN
HUMAN CELL
HUMAN IMMUNODEFICIENCY VIRUS 1
INTERLEUKIN 6
L SELECTIN
LEUKOCYTE ACTIVATION
MALE
MARKER
MDA5 PROTEIN
MESSENGER RNA
NORMAL HUMAN
PRIORITY JOURNAL
REACTIVE OXYGEN METABOLITE
RETINOIC ACID INDUCIBLE PROTEIN I
SINGLE STRANDED RNA
TOLL LIKE RECEPTOR 2
TOLL LIKE RECEPTOR 4
TOLL LIKE RECEPTOR 7
TOLL LIKE RECEPTOR 8
TUMOR NECROSIS FACTOR
UNCLASSIFIED DRUG
- Rights
- openAccess
- License
- http://purl.org/coar/access_right/c_abf2
Summary: | Neutrophils are key effector cells of the innate immune system and are involved in the host defense against invading pathogens such as viruses. Recently, it was reported that HIV-1–neutrophil interaction triggers neutrophil activation and promotes expression of Toll-like receptors (TLRs). Here, we assessed the role of single-stranded RNA40 (ssRNA40) derived from HIV-1 in neutrophil activation. We observed functional activation of neutrophils in response to HIV-1-derived ssRNA40 based on the expression of TLR7/8, RIG-I, and MDA5, induction of cytokines (IL-6 and TNF-a), and the production of reactive oxygen species (ROS). Additionally, ssRNA40 promoted the expression of CD62L and TNF-a and the production of ROS in the presence of the TLR2 agonist Pam2CSK4. ssRNA40 together with R848 (a TLR7/8 agonist) increased CD11b expression but decreased CD62L expression. Furthermore, decreased IL-6 expression was observed in the presence of the TLR4 agonist LPS. Finally, we found that ssRNA40 promotes RIG-I and MDA5 expression in the presence of the TLR2, TLR4 and TLR7/8 agonists. This study demonstrates a functional response of TLRs in neutrophils challenged with ssRNA40, suggesting that TLRs could be involved in the innate immune response observed during HIV infection, which might be mediated by its genome. © 2016, Springer Science+Business Media New York. |
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