Kaposi's sarcoma-associated herpesvirus and extracellular vesicles.

Kaposi's sarcoma Kaposi's sarcoma-associated herpesvirus extracellular vesicles microRNA primary effusion lymphoma

Journal

Journal of medical virology
ISSN: 1096-9071
Titre abrégé: J Med Virol
Pays: United States
ID NLM: 7705876

Informations de publication

Date de publication:
06 2021
Historique:
revised: 04 01 2021
received: 15 12 2020
accepted: 05 01 2021
pubmed: 9 1 2021
medline: 9 10 2021
entrez: 8 1 2021
Statut: ppublish

Résumé

Kaposi's sarcoma-associated herpesvirus (KSHV) represents the etiological agent for several human malignancies, including Kaposi's Sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castleman's disease (MCD), which develop mainly in immunocompromised patients. KSHV has established many strategies to hijack and thwart the host's immune responses, including through the use of extracellular vesicles (EVs). EVs represent a significant mode of intercellular communication as they carry a variety of molecules that can be delivered from cell-to-cell. EVs are now recognized as one of the major players in immune system development and function during both innate and adaptive immune responses. In the current mini-review, we summarize recent findings on how KSHV utilizes EVs to create favorable environments for viral spread and persistence while evading immune responses. We also discuss the limitations and unanswered questions in this field and the potential areas for related immunotherapies.

Identifiants

pubmed: 33415746
doi: 10.1002/jmv.26780
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

3294-3299

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

Urbanellirbanelli L, Buratta S, Tancini B, et al. The role of extracellular vesicles in viral infection and transmission. Vaccines. 2019;7:102. https://doi.org/10.3390/vaccines7030102
Maas SLN, Breakefield XO, Weaver AM. Extracellular vesicles: unique intercellular delivery vehicles. Trends Cell Biol. 2017;27:172-188. https://doi.org/10.1016/j.tcb.2016.11.003
Kim MK, Abdelmohsen K, Mustapic M, Kapogiannis D, Gorospe M. RNA in extracellular vesicles. Wiley Interdiscip Rev. 2017;8:8. https://doi.org/10.1002/wrna.1413
Kalraalra H, Simpson RJ, Ji H, et al. Vesiclepedia: a compendium for extracellular vesicles with continuous community annotation. PLOS Biol. 2012;10:10. https://doi.org/10.1371/journal.pbio.1001450
Mathivanan S, Fahner CJ, Reid GE, Simpson RJ. ExoCarta 2012: database of exosomal proteins, RNA and lipids. Nucleic Acids Res. 2012;40:1241-1244. https://doi.org/10.1093/nar/gkr828
Kimim DK, Lee J, Kim SR, et al. EVpedia: a community web portal for extracellular vesicles research. Bioinformatics. 2015;31:933-939. https://doi.org/10.1093/bioinformatics/btu741
Hoen EN, Cremer T, Gallo RC, Margolis LB. Extracellular vesicles and viruses: are they close relatives? Proc Natl Acad Sci USA. 2016;113:9155-9161. https://doi.org/10.1073/pnas.1605146113
Broussard G, Damania B. KSHV: immune modulation and immunotherapy. Front Immunol. 2020;10:3084. https://doi.org/10.3389/fimmu.2019.03084
Vangipuram R, Tyring SK. AIDS-associated malignancies. Cancer Treat Res. 2019;177:1-21. https://doi.org/10.1007/978-3-030-03502-0_1
Mesri EA, Cesarman E, Boshoff C. Kaposi's sarcoma and its associated herpesvirus. Nat Rev Cancer. 2010;10:707-719. https://doi.org/10.1038/nrc2888
McNamara RP, Chugh PE, Bailey A, et al. Extracellular vesicles from Kaposi Sarcoma-associated herpesvirus lymphoma induce long-term endothelial cell reprogramming. PLOS Pathog. 2019;15:2. https://doi.org/10.1371/journal.ppat.1007536
Zhang Y, Liu Y, Liu H, Tang WH. Exosomes: biogenesis, biologic function and clinical potential. Cell & Bioscience. 2019;9:19. https://doi.org/10.1186/s13578-019-0282-2
Henne WM, Buchkovich NJ, Emr SD. The ESCRT pathway. Dev Cell. 2011;21:77-91. https://doi.org/10.1016/j.devcel.2011.05.015
Airola MV, Hannun YA. Sphingolipid metabolism and neutral sphingomyelinases. Handb Exp Pharmacol. 2013;215:57-76. https://doi.org/10.1007/978-3-7091-1368-4_3
Castro BM, Prieto M, Silva LC. Ceramide: a single sphingolipid with unique biophysical properties. Prog Lipid Res. 2014;54:53-67. https://doi.org/10.1016/j.plipres.2014.01.004
Perez-Hernandez D, Gutiérrez-Vázquez C, Jorge I, et al. The intracellular interactome of tetraspanin-enriched microdomains reveals their function as sorting machineries toward exosomes. J Biol Chem. 2013;288:11649-11661. https://doi.org/10.1074/jbc.M112.445304
van den Boorn JG, Dassler J, Coch C, Schlee M, Hartmann G. Exosomes as nucleic acid nanocarriers. Adv Drug Deliv Rev. 2013;65:331-335. https://doi.org/10.1016/j.addr.2012.06.011
Robbins PD, Morelli AE. Regulation of immune responses by extracellular vesicles. Nat Rev Immunol. 2014;14:195-208. https://doi.org/10.1038/nri3622
Ostrowski M, Carmo NB, Krumeich S, et al. Rab27a and Rab27b control different steps of the exosome secretion pathway. Nat Cell Biol. 2010;12:19-30. https://doi.org/10.1038/ncb2000
Fader CM, Colombo MI. Autophagy and multivesicular bodies: two closely related partners. Cell Death and Differ. 2009;16:70-78. https://doi.org/10.1038/cdd.2008.168
Spiller OB, Mark L, Blue CE, et al. Dissecting the regions of virion-associated Kaposi's sarcoma-associated herpesvirus complement control protein required for complement regulation and cell binding. J Virol. 2006;80:4068-4078. https://doi.org/10.1128/JVI.80.8.4068-4078.2006
Jeon H, Yoo S, Choi HS, et al. Extracellular vesicles from KSHV-infected endothelial cells activate the complement system. Oncotarget. 2017;8:99841-99860. https://doi.org/10.18632/oncotarget.21668
Zhu FX, Sathish N, Yuan Y. Antagonism of host antiviral responses by Kaposi's sarcoma-associated herpesvirus tegument protein ORF45. PLOS One. 2010;5:5. https://doi.org/10.1371/journal.pone.0010573
Jeon H, Lee J, Lee S, et al. Extracellular vesicles from KSHV-infected cells stimulate antiviral immune response through mitochondrial DNA. Front Immunol. 2019:24. https://doi.org/10.3389/fimmu.2019.00876
Singh VV, Kerur N, Bottero V, et al. Kaposi's sarcoma-associated herpesvirus latency in endothelial and B cells activates gamma interferon-inducible protein 16-mediated inflammasomes. J Virol. 2013;87:4417-4431. https://doi.org/10.1128/JVI.03282-12
Hansen A, Henderson S, Lagos D, et al. KSHV-encoded miRNAs target MAF to induce endothelial cell reprogramming. Genes Dev. 2010;24:195-205. https://doi.org/10.1101/gad.553410
Lei X, Bai Z, Ye F, et al. Regulation of NF-kappaB inhibitor IkappaBalpha and viral replication by a KSHV microRNA. Nat Cell Biol. 2010;12:193-199. https://doi.org/10.1038/ncb2019
Haecker I, Gay LA, Yang Y, et al. Ago HITS-CLIP expands understanding of Kaposi's sarcoma-associated herpesvirus miRNA function in primary effusion lymphomas. PLOS Pathog. 2012:8. https://doi.org/10.1371/annotation/bb6f7450-8506-41c3-8519-020df8b382b9
Samols MA, Skalsky RL, Maldonado AM, et al. Identification of cellular genes targeted by KSHV-encoded microRNAs. PLOS Pathog. 2007:3. https://doi.org/10.1371/journal.ppat.0030065
Qin Z, Freitas E, Sullivan R, et al. Upregulation of xCT by KSHV-encoded microRNAs facilities KSHV dissemination and persistence in an environment of oxidative stress. PLOS Pathog. 2010:6. https://doi.org/10.1371/journal.ppat.1000742
Gottwein E, Corcoran DL, Mukherjee N, et al. Viral microRNA targetome of KSHV-infected primary effusion lymphoma cell lines. Cell Host Microbe. 2011;10:515-526. https://doi.org/10.1016/j.chom.2011.09.012
Chugh PE, Sin SH, Ozgur S, et al. Systemically circulating viral and tumor-derived microRNAs in KSHV-associated malignancies. PLOS Pathog. 2013;9:7. https://doi.org/10.1371/journal.ppat.1003484
Hoshina S, Sekizuka T, Kataoka M, et al. Profile of exosomal and intracellular mircoRNA in gamma-herpesvirus-infected lymphoma cell lines. PLOS One. 2016;11:11. https://doi.org/10.1371/journal.pone.0162574
Cheng F, Pekkonen P, Laurinavicius S, et al. KSHV-initiated notch activation leads to membrane-type-1 matrix metalloproteinase-dependent lymphatic endothelial-to-mesenchymal transition. Cell Host Microbe. 2011;10:577-590. https://doi.org/10.1016/j.chom.2011.10.011
Sychev ZE, Hu A, DiMaio TA, et al. Integrated systems biology analysis of KSHV latent infection reveals viral induction and reliance on peroxisome mediated lipid metabolism. PLOS Pathog. 2017;13:13. https://doi.org/10.1371/journal.ppat.1006256
Meckes DG, Gunawardena HP, Dekroon RM, et al. Modulation of B-cell exosome proteins by gamma herpesvirus infection. Proc Natl Acad Sci USA. 2013;110:2925-2933. https://doi.org/10.1073/pnas.1303906110
Altenberg B, Greulich KO. Genes of glycolysis are ubiquitously overexpressed in 24 cancer classes. Genomics. 2004;84:1014-1020. https://doi.org/10.1016/j.ygeno.2004.08.010
Kondoh H, Lleonart ME, Gil J, et al. Glycolytic enzymes can modulate cellular life span. Cancer Res. 2005;65:177-185.
Anticoli S, Manfredi F, Chiozzini C, et al. An exosome-based vaccine platform imparts cytotoxic T lymphocyte immunity against viral antigens. Biotechnol J. 2018;13:13. https://doi.org/10.1002/biot.201700443
Datta A, Kim H, McGee L, et al. High-throughput screening identified selective inhibitors of exosome biogenesis and secretion: a drug repurposing strategy for advanced cancer. Sci Rep. 2018;8:8161. https://doi.org/10.1038/s41598-018-26411-7

Auteurs

Lindsey Barrett (L)

Department of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.

Lu Dai (L)

Department of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.

Shanzhi Wang (S)

Department of Chemistry, University of Arkansas at Little Rock, Little Rock, Arkansas, USA.

Zhiqiang Qin (Z)

Department of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.

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