Hypoxia, Leptin, and Vascular Endothelial Growth Factor Stimulate Vascular Endothelial Cell Differentiation of Human Adipose Tissue-Derived Stem Cells

Abstract

The plasticity of human adipose tissue-derived stem cells (hASCs) is promising, but differentiation in vitro toward endothelial cells is poorly understood. Flow cytometry demonstrated that hASCs isolated from excised fat tissue were positive for CD29, CD44, CD70, CD90, CD105, and CD166 and negative for the endothelial marker CD31, and the hematopoietic cell markers CD34 and CD133. hASCs differentiated into adipocytes after cultivation in adipogenic medium. Exposure of hASCs for 10 days under hypoxia (3% oxygen) in combination with leptin increased the percentage of CD31(+) endothelial cells as well as CD31, VE-Cadherin, Flk-1, Tie2, von Willebrand factor, and endothelial cell nitric oxide synthase mRNA expression. This was enhanced on co-incubation of vascular endothelial growth factor (VEGF) and leptin, whereas VEGF alone was not sufficient. Moreover, hASCs cultured on a matrigel surface under hypoxia/VEGF/leptin, showed a stable branching network. Hypoxic conditions significantly decreased apoptosis as evaluated by cleaved caspase-3, and increased prolyl hydroxylase domain 3 mRNA expression. Hypoxia increased expression of VEGF as well as leptin transcripts, which were significantly inhibited on co-incubation with either VEGF or leptin or a combination of both. Furthermore, leptin treatment of hypoxic cells increased the expression of the long/signaling form of the leptin receptor (ObRL), which was augmented on co-incubation with VEGF. The observed endothelial differentiation was dependent on the Akt pathway, as co-administration with Akt inhibitor abolished the observed effects. In conclusion, our data demonstrate that hASCs can be efficiently differentiated to endothelial cells by mimicking the hypoxic and pro-angiogenic microenvironment of adipose tissue.

The Biomolecular Basis of Adipogenic Differentiation of Adipose-Derived Stem Cells

“…NGF and its precursor proNGF are apoptotic inducers of vascular cells [40]. The exposure of ASCs for 10 days to hypoxia in combination with leptin increased the percentage of CD31 + endothelial cells as well as CD31, VE-Cadherin, Flk-1, Tie2, von Willebrand factor, and endothelial cell nitric oxide synthase mRNA [41]. The transcription of these angiogenic markers was further enhanced by co-incubation of VEGF and leptin, and human ASCs cultured on a matrigel surface under hypoxia/VEGF/leptin showed a stable branching network [41].…”

Comparison of Endothelial Differentiation Capacities of Human and Rat Adipose-Derived Stem Cells

“…10,[13][14][15][16][17][18][19][20] However, it is still not clear whether human adipose-derived stem cells have the endothelial differentiation capacity that might be of clinical significance, under the same differentiation conditions.…”

Comparison of Endothelial Differentiation Capacities of Human and Rat Adipose-Derived Stem Cells: Correction

“…In addition, use of methods such as the application of shear stress, 29,33,34 highly resistant thermoplastic sacrificial templates, 33 nanostructured surfaces, 35,36 chemicals such as sphingosine-1-phosphate and leptin, 22,37,38 and hypoxic preconditioning 15,22 may further increase the endothelial differentiation capacity of human adipose-derived stem cells.…”