ASC and SVF Cells Synergistically Induce Neovascularization in Ischemic Hindlimb Following Cotransplantation.
Hong Zhe ZhangDong Sik ChaeSung-Whan KimPublished in: International journal of molecular sciences (2021)
Previously, we reported the angio-vasculogenic properties of human stromal vascular fraction (SVF) and adipose tissue-derived mesenchymal stem cells (ASCs). In this study, we investigated whether the combination of ASCs and SVF cells exhibited synergistic angiogenic properties. We conducted quantitative (q)RT-PCR, Matrigel plug, tube formation assays, and in vivo therapeutic assays using an ischemic hind limb mouse model. Immunohistochemical analysis was also conducted. qRT-PCR results revealed that FGF-2 was highly upregulated in ASCs compared with SVF, while PDGF-b and VEGF-A were highly upregulated in SVF. Conditioned medium from mixed cultures of ASCs and SVF (A+S) cells showed higher Matrigel tube formation and endothelial cell proliferation in vitro. A+S cell transplantation into ischemic mouse hind limbs strongly prevented limb loss and augmented blood perfusion compared with SVF cell transplantation. Transplanted A+S cells also showed high capillary density, cell proliferation, angiogenic cytokines, and anti-apoptotic potential in vivo compared with transplanted SVF. Our data indicate that A+S cell transplantation results in synergistic angiogenic therapeutic effects. Accordingly, A+S cell injection could be an alternative therapeutic strategy for treating ischemic diseases.
Keyphrases
- induced apoptosis
- cell cycle arrest
- single cell
- cell therapy
- cell proliferation
- adipose tissue
- mouse model
- endothelial cells
- cell death
- stem cells
- high throughput
- ischemia reperfusion injury
- endoplasmic reticulum stress
- metabolic syndrome
- oxidative stress
- cell cycle
- mesenchymal stem cells
- bone marrow
- magnetic resonance
- cancer therapy
- vascular endothelial growth factor
- high resolution
- computed tomography
- high fat diet
- single molecule
- data analysis
- angiotensin ii