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Conditioned media from human adipose-derived stem cell culture in some stressed culture conditions differ angiogenic potential

Ngoc Bich Vu 1, 2, * ORCID logo
Binh Thanh Vu 1, 2
Khanh Nha Nguyen 1, 2 ORCID logo
Phuc Van Pham 1, 2 ORCID logo
  1. Stem Cell Institute, University of Science Ho Chi Minh City, Viet Nam
  2. Viet Nam National University Ho Chi Minh City, Viet Nam
Correspondence to: Ngoc Bich Vu, Stem Cell Institute, University of Science Ho Chi Minh City, Viet Nam; Viet Nam National University Ho Chi Minh City, Viet Nam. ORCID: https://orcid.org/0000-0003-4447-9212. Email: [email protected].
Volume & Issue: Vol. 8 No. 6 (2021) | Page No.: 4423-4433 | DOI: 10.15419/bmrat.v8i6.680
Published: 2021-06-30

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This article is published with open access by BioMedPress. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. 

Abstract

Introduction: The potency of mesenchymal stem cells (MSCs) related to their biological effects includes immune modulation and angiogenesis. Recently, some stress conditions were applied to enhance the angiogenic potential of MSCs. This study aimed to assess the effects of conditioned media (CM) collected from adipose-derived stem cells’ (ADSCs’) culture under various stress conditions on angiogenesis in vitro.

Methods: ADSCs were isolated and expanded according to a published protocol. These cells were treated with some stress conditions including hypoxia, starvation, a combination of hypoxia and starvation, and TNF-alpha treatment. CM from these cultures were collected and used for further experiments. The angiogenic potential of CM was evaluated through stimulation of HUVECs to form vessels in vitro. ELISA was used to measure the VEGF concentrations in CM.

Results: CM-derived various stress ADSC cultures differently affected angiogenesis of HUVECs. The supernatant from a hypoxic culture of ADSCs contained the highest concentration of VEGF and was higher than normoxic culture. However, in others, VEGF concentrations in CM significantly reduced compared to control. CM from TNF-alpha treatment failed to support the formation of blood vessels from HUVECs, while other conditions could support blood vessel formation in vitro. TNF-alpha dually affected both ADSCs and HUVECs. Furthermore, TNF-alpha could stimulate or suppress the VEGF production in dose-response in ADSCs and cause apoptosis in HUVECs at high concentrations.

Conclusion: CM from the hypoxic culture of ADSCs contained a high concentration of VEGF, supporting angiogenesis of HUVECs well. This is a simple technique that can be used in translational applications. However, the use of TNF-alpha yielded dual effects on ADSCs and HUVECs. Although the VEGF production was enhanced at a low dose of TNF-alpha, they could induce apoptosis in endothelial cells to cause the failure of angiogenesis.

 

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