Uptake of lymphoma-derived exosomes by peripheral blood leukocytes

Heather R Ferguson Bennit,1,2 Amber Gonda,1,3 Laura J Oppegard,2 David P Chi,2 Salma Khan,1,2 Nathan R Wall1,2 1Center for Health Disparities & Molecular Medicine, 2Division of Biochemistry, Department of Basic Sciences, 3Department of Anatomy, Loma Linda University School of Medicine, Loma...

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Autores principales: Ferguson Bennit HR, Gonda A, Oppegard LJ, Chi DP, Khan S, Wall NR
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Lenguaje:EN
Publicado: Dove Medical Press 2017
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Acceso en línea:https://doaj.org/article/e27be11b6e8a4394aa98420de140a8dc
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spelling oai:doaj.org-article:e27be11b6e8a4394aa98420de140a8dc2021-12-02T02:29:11ZUptake of lymphoma-derived exosomes by peripheral blood leukocytes1179-9889https://doaj.org/article/e27be11b6e8a4394aa98420de140a8dc2017-02-01T00:00:00Zhttps://www.dovepress.com/uptake-of-lymphoma-derived-exosomes-by-peripheral-blood-leukocytes-peer-reviewed-article-BLCTThttps://doaj.org/toc/1179-9889Heather R Ferguson Bennit,1,2 Amber Gonda,1,3 Laura J Oppegard,2 David P Chi,2 Salma Khan,1,2 Nathan R Wall1,2 1Center for Health Disparities & Molecular Medicine, 2Division of Biochemistry, Department of Basic Sciences, 3Department of Anatomy, Loma Linda University School of Medicine, Loma Linda, CA, USA Abstract: Exosomes are nanosized lipid vesicles secreted into blood and other body fluids and serve as vehicles for intercellular communication. Despite being an important component of the tumor microenvironment (TME), exosomal targeting and uptake into recipient cells are still not fully understood. Few studies have looked at lymphoma exosomes and their interactions with circulating blood cells. In this study, we examine the exosomal uptake distribution among peripheral blood leukocytes (PBLs) using vesicles derived from a diffuse large B cell lymphoma cell line, WSU-DLCL2. Lymphoma cells survive, proliferate, and are protected from the cytotoxic effects of chemotherapeutic agents by soluble factors or by direct contact with inflammatory and stromal cells within the TME. In an attempt to close the gap in knowledge concerning lymphoma TME immunosuppression, we have treated normal human PBLs with PKH67-labeled lymphoma exosomes and monitored the uptake by measuring fluorescence at different time points using flow cytometry and fluorescent microscopy. Our results show that of the four populations examined, B cells and monocytes demonstrated uptake of PKH67-labeled exosomes, while T cells and NK cells displayed significantly less uptake. Keywords: exosome, non-Hodgkin’s lymphoma, B cellFerguson Bennit HRGonda AOppegard LJChi DPKhan SWall NRDove Medical Pressarticleexosomenon-Hodgkin’s lymphomaB cellDiseases of the blood and blood-forming organsRC633-647.5ENBlood and Lymphatic Cancer: Targets and Therapy, Vol Volume 7, Pp 9-23 (2017)
institution DOAJ
collection DOAJ
language EN
topic exosome
non-Hodgkin’s lymphoma
B cell
Diseases of the blood and blood-forming organs
RC633-647.5
spellingShingle exosome
non-Hodgkin’s lymphoma
B cell
Diseases of the blood and blood-forming organs
RC633-647.5
Ferguson Bennit HR
Gonda A
Oppegard LJ
Chi DP
Khan S
Wall NR
Uptake of lymphoma-derived exosomes by peripheral blood leukocytes
description Heather R Ferguson Bennit,1,2 Amber Gonda,1,3 Laura J Oppegard,2 David P Chi,2 Salma Khan,1,2 Nathan R Wall1,2 1Center for Health Disparities & Molecular Medicine, 2Division of Biochemistry, Department of Basic Sciences, 3Department of Anatomy, Loma Linda University School of Medicine, Loma Linda, CA, USA Abstract: Exosomes are nanosized lipid vesicles secreted into blood and other body fluids and serve as vehicles for intercellular communication. Despite being an important component of the tumor microenvironment (TME), exosomal targeting and uptake into recipient cells are still not fully understood. Few studies have looked at lymphoma exosomes and their interactions with circulating blood cells. In this study, we examine the exosomal uptake distribution among peripheral blood leukocytes (PBLs) using vesicles derived from a diffuse large B cell lymphoma cell line, WSU-DLCL2. Lymphoma cells survive, proliferate, and are protected from the cytotoxic effects of chemotherapeutic agents by soluble factors or by direct contact with inflammatory and stromal cells within the TME. In an attempt to close the gap in knowledge concerning lymphoma TME immunosuppression, we have treated normal human PBLs with PKH67-labeled lymphoma exosomes and monitored the uptake by measuring fluorescence at different time points using flow cytometry and fluorescent microscopy. Our results show that of the four populations examined, B cells and monocytes demonstrated uptake of PKH67-labeled exosomes, while T cells and NK cells displayed significantly less uptake. Keywords: exosome, non-Hodgkin’s lymphoma, B cell
format article
author Ferguson Bennit HR
Gonda A
Oppegard LJ
Chi DP
Khan S
Wall NR
author_facet Ferguson Bennit HR
Gonda A
Oppegard LJ
Chi DP
Khan S
Wall NR
author_sort Ferguson Bennit HR
title Uptake of lymphoma-derived exosomes by peripheral blood leukocytes
title_short Uptake of lymphoma-derived exosomes by peripheral blood leukocytes
title_full Uptake of lymphoma-derived exosomes by peripheral blood leukocytes
title_fullStr Uptake of lymphoma-derived exosomes by peripheral blood leukocytes
title_full_unstemmed Uptake of lymphoma-derived exosomes by peripheral blood leukocytes
title_sort uptake of lymphoma-derived exosomes by peripheral blood leukocytes
publisher Dove Medical Press
publishDate 2017
url https://doaj.org/article/e27be11b6e8a4394aa98420de140a8dc
work_keys_str_mv AT fergusonbennithr uptakeoflymphomaderivedexosomesbyperipheralbloodleukocytes
AT gondaa uptakeoflymphomaderivedexosomesbyperipheralbloodleukocytes
AT oppegardlj uptakeoflymphomaderivedexosomesbyperipheralbloodleukocytes
AT chidp uptakeoflymphomaderivedexosomesbyperipheralbloodleukocytes
AT khans uptakeoflymphomaderivedexosomesbyperipheralbloodleukocytes
AT wallnr uptakeoflymphomaderivedexosomesbyperipheralbloodleukocytes
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