» Articles » PMID: 33304471

Hypoxia and Extracellular Vesicles: A Review on Methods, Vesicular Cargo and Functions

Overview
Publisher Wiley
Date 2020 Dec 11
PMID 33304471
Citations 92
Authors
Affiliations
Soon will be listed here.
Abstract

Hypoxia is an essential hallmark of several serious diseases such as cardiovascular and metabolic disorders and cancer. A decline in the tissue oxygen level induces hypoxic responses in cells which strive to adapt to the changed conditions. A failure to adapt to prolonged or severe hypoxia can trigger cell death. While some cell types, such as neurons, are highly vulnerable to hypoxia, cancer cells take advantage of a hypoxic environment to undergo tumour growth, angiogenesis and metastasis. Hypoxia-induced processes trigger complex intercellular communication and there are now indications that extracellular vesicles (EVs) play a fundamental role in these processes. Recent developments in EV isolation and characterization methodology have increased the awareness of the importance of EV purity in functional and cargo studies. Cell death, a hallmark of severe hypoxia, is a known source of intracellular contaminants in isolated EVs. In this review, methodological aspects of studies investigating hypoxia-induced EVs are critically evaluated. Key concerns and gaps in the current knowledge are highlighted and future directions for studies are set. To accelerate and advance research, an in-depth analysis of the functions and cargo of hypoxic EVs, compared to normoxic EVs, is provided with the focus on the altered microRNA contents of the EVs.

Citing Articles

Adipose-derived stem cells using fibrin gel as a scaffold enhances post-hepatectomy liver regeneration.

Imamura H, Tomimaru Y, Kobayashi S, Harada A, Kita S, Sasaki K Sci Rep. 2025; 15(1):6334.

PMID: 39984656 PMC: 11845764. DOI: 10.1038/s41598-025-90805-7.


Pathways and outputs orchestrated in tumor microenvironment cells by hypoxia-induced tumor-derived exosomes in pan-cancer.

Capik O, Karatas O Cell Oncol (Dordr). 2025; .

PMID: 39928285 DOI: 10.1007/s13402-025-01042-z.


Could hypoxic conditioning augment the potential of mesenchymal stromal cell-derived extracellular vesicles as a treatment for type 1 diabetes?.

Forkan C, Shrestha A, Yu A, Chuang C, Pociot F, Yarani R Stem Cell Res Ther. 2025; 16(1):37.

PMID: 39901225 PMC: 11792614. DOI: 10.1186/s13287-025-04153-4.


Blood-derived APLP1 extracellular vesicles are potential biomarkers for the early diagnosis of brain diseases.

Choi Y, Park J, Jo A, Lim C, Park J, Hwang J Sci Adv. 2025; 11(1):eado6894.

PMID: 39742488 PMC: 11691634. DOI: 10.1126/sciadv.ado6894.


Hypoxic Human Microglia Promote Angiogenesis Through Extracellular Vesicle Release.

Testa A, Vignozzi L, Corallo D, Aveic S, Viola A, Allegra M Int J Mol Sci. 2024; 25(23).

PMID: 39684220 PMC: 11641038. DOI: 10.3390/ijms252312508.


References
1.
Xu H, Yuan Y, Wu W, Zhou M, Jiang Q, Niu L . Hypoxia stimulates invasion and migration of human cervical cancer cell lines HeLa/SiHa through the Rab11 trafficking of integrin αvβ3/FAK/PI3K pathway-mediated Rac1 activation. J Biosci. 2018; 42(3):491-499. DOI: 10.1007/s12038-017-9699-0. View

2.
Zhang S, Liu L, Wang R, Tuo H, Guo Y, Yi L . MicroRNA-217 promotes angiogenesis of human cytomegalovirus-infected endothelial cells through downregulation of SIRT1 and FOXO3A. PLoS One. 2013; 8(12):e83620. PMC: 3869804. DOI: 10.1371/journal.pone.0083620. View

3.
Umezu T, Tadokoro H, Azuma K, Yoshizawa S, Ohyashiki K, Ohyashiki J . Exosomal miR-135b shed from hypoxic multiple myeloma cells enhances angiogenesis by targeting factor-inhibiting HIF-1. Blood. 2014; 124(25):3748-57. PMC: 4263983. DOI: 10.1182/blood-2014-05-576116. View

4.
Takov K, Yellon D, Davidson S . Comparison of small extracellular vesicles isolated from plasma by ultracentrifugation or size-exclusion chromatography: yield, purity and functional potential. J Extracell Vesicles. 2019; 8(1):1560809. PMC: 6327926. DOI: 10.1080/20013078.2018.1560809. View

5.
Santangelo L, Giurato G, Cicchini C, Montaldo C, Mancone C, Tarallo R . The RNA-Binding Protein SYNCRIP Is a Component of the Hepatocyte Exosomal Machinery Controlling MicroRNA Sorting. Cell Rep. 2016; 17(3):799-808. DOI: 10.1016/j.celrep.2016.09.031. View