# Isolation of endothelial progenitor cells from human adipose tissue

**Authors:** Cristina Caccioppoli, Rossella D’Oria, Valentina Annamaria Genchi, Giuseppe Palma, Valentina Andrulli Buccheri, Isabella Calderoni, Carmen Tedesco, Carmela Colabufo, Nicola Marrano, Giuseppina Biondi, Nada Chaoul, Antonio Braun, Angela Pezzolla, Angelo Cignarelli, Annalisa Natalicchio, Luigi Laviola, Francesco Giorgino, Sebastio Perrini

PMC · DOI: 10.1038/s41366-025-01884-5 · International Journal of Obesity (2005) · 2025-08-23

## TL;DR

The paper describes a method to isolate endothelial progenitor cells from human adipose tissue, which could be useful for regenerative medicine.

## Contribution

A new method for isolating and characterizing endothelial progenitor cells from human adipose tissue is presented.

## Key findings

- CD31+ cells from SVF-II showed higher expression of endothelial markers and endothelial-like morphology.
- CD31+ cells expressed vWF, VE-Cadherin, and had high mRNA levels of E-selectin, e-NOS, VEGFR, and CD34.
- CD31+ cells demonstrated functional properties like tube formation and acetylated LDL uptake.

## Abstract

Endothelial progenitor cells (EPCs) play an important role in angiogenic responses in multiple tissues and mediate a coordinate augmentation of the capillary network as adipose tissue (AT) expands in response to positive energy balance. However, the isolation and culture of EPCs from human AT has proven difficult so far. Here, we report the isolation and characterization of EPCs from human AT (AT-EPCs).

Omental and subcutaneous AT specimens (approximately 1-2 g) were obtained during abdominal surgery. Following AT digestion with collagenase, both the filtered (SVF-I) and unfiltered (SVF-II) stromal vascular fractions (SVF) of AT were used. Expression of endothelial markers, such as CD31 and VE-Cadherin, was analyzed by using flow cytometry. Both SVF-I and SVF-II fractions were used for magnetic-based enrichment of endothelial cells using anti-human CD31 beads. Immunofluorescence staining, immunoblotting, and quantitative real-time PCR were performed to analyze expression of endothelial markers. Functional assays, including matrigel-based capillary-like tube formation assay and acetylated LDL uptake assays, were also performed.

CD31 and VE-Cadherin were more expressed in SVF-II than SVF-I. CD31+ cells from SVF-II exhibited an endothelial-like cobblestone morphology. The CD31+ fraction also expressed Von Willebrand Factor (vWF) and VE-Cadherin. High mRNA levels of E-selectin, e-NOS, VEGFR, and CD34 were found in CD31+ cells, and E-selectin and e-NOS proteins were readily detectable. In addition, CD31+ cells were able to form tubes and incorporate acetylated LDL in vitro.

Large amounts of AT-EPCs with distinct functional properties can be isolated from omental and subcutaneous adipose tissue.

## Linked entities

- **Genes:** PECAM1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 5175], cdh5 (cadherin 5) [NCBI Gene 100488458], VWF (von Willebrand factor) [NCBI Gene 7450], Sele (selectin, endothelial cell) [NCBI Gene 20339], NOS3 (nitric oxide synthase 3) [NCBI Gene 4846], KDR (kinase insert domain receptor) [NCBI Gene 3791], CD34 (CD34 molecule) [NCBI Gene 947]
- **Proteins:** PECAM1 (platelet and endothelial cell adhesion molecule 1), cdh5 (cadherin 5), Sele (selectin, endothelial cell), NOS3 (nitric oxide synthase 3)

## Full-text entities

- **Genes:** KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, VWF (von Willebrand factor) [NCBI Gene 7450] {aka F8VWF, VWD}, CDH5 (cadherin 5) [NCBI Gene 1003] {aka 7B4, CD144}, SELE (selectin E) [NCBI Gene 6401] {aka CD62E, ELAM, ELAM1, ESEL, LECAM2, selectin-e}, PECAM1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 5175] {aka CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM}, NOS3 (nitric oxide synthase 3) [NCBI Gene 4846] {aka EC-NOS, ECNOS, MYMY8, NOSIII, cNOS, eNOS}, CD34 (CD34 molecule) [NCBI Gene 947]
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** SVF-II — Mus musculus (Mouse), Stromal cell line (CVCL_D134)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12634424/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12634424/full.md

## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12634424/full.md

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Source: https://tomesphere.com/paper/PMC12634424