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Updated: May 31, 2026

Isolation of Perivascular Multipotent Precursor Cell Populations from Human Cardiac Tissue
Published on: October 8, 2016
Mesenchymal stem cells in infantile hemangioma reside in the perivascular region
Si-Ming Yuan1, Rong-Liang Chen, Wei-Min Shen
1Department of Pathology, Jinling Hospital, Medical School of Nanjing University, Nanjing, Jiangsu, China.
Abstract:
Infantile hemangioma grows quickly in the first year of life and regresses slowly to fibrofatty tissue during childhood; mesenchymal stem cells (MSCs) have been reported to contribute to this adipogenesis. Recent studies have shown the perivascular origin of MSCs in multiple organs. We hypothesized that MSCs in hemangioma might also reside in the perivascular region. We isolated MSCs from proliferating hemangioma by their selective adhesion to plastic culture dishes. Mesenchymal stem cells from bone marrow (BM-MSCs) and foreskin-derived fibroblasts were used as controls. Flow cytometry and immunofluorescence staining were used to examine their antigen profiles; in vitro induction of multi-lineage differentiation was performed to test their pluripotency. Platelet-derived growth factor R-β (PDGFR-β), CD133, and peroxisome-proliferator-activated receptor gamma (PPAR-γ) were selected as the markers to observe MSCs in hemangioma by immunohistochemistry staining, with costaining of CD31 and alpha-smooth muscle actin (α-SMA). Hemangioma-derived MSCs (Hem-MSCs) had fibroblast-like morphology; they expressed the MSC markers CD105, CD90, CD29, and vimentin and did not express the hematopoietic/endothelial markers CD45, CD34, CD31, and flt-1; Hem-MSCs also expressed CD133 and PPAR-γ. Most Hem-MSCs expressed PDGFR-β and α-SMA; in contrast, the expression of PDGFR-β and α-SMA in BM-MSCs was very weak. The Hem-MSCs differentiated into adipocytes, osteoblasts, and chondroblasts in vitro. This confirmed their pluripotency. Immunohistochemistry showed the colocalization of PDGFR-β/α-SMA, CD133/α-SMA, and PPAR-γ/α-SMA in the perivascular region. MSCs were successfully obtained from proliferating hemangioma, revealing the perivascular origin of MSCs in hemangioma.
Insights
Mesenchymal stem cells (MSCs) from infantile hemangioma reside in perivascular regions. These hemangioma-derived MSCs possess multipotent differentiation capabilities, confirming their origin and potential role in hemangioma development.
Area of Science:
- Regenerative Medicine
- Developmental Biology
- Cell Biology
Background:
- Infantile hemangioma (IH) is a common pediatric vascular tumor characterized by rapid proliferation followed by slow regression.
- Mesenchymal stem cells (MSCs) are implicated in the adipogenesis of regressing hemangiomas.
- Recent research suggests MSCs originate from perivascular niches in various tissues.
Purpose of the Study:
- To investigate the potential perivascular origin of MSCs within proliferating infantile hemangiomas.
- To characterize hemangioma-derived MSCs (Hem-MSCs) and assess their multipotency.
- To identify specific markers for Hem-MSCs in their native perivascular environment.
Main Methods:
- Isolation and culture of MSCs from proliferating hemangioma tissue.
- Characterization of Hem-MSCs using flow cytometry and immunofluorescence for specific cell markers (e.g., PDGFR-β, CD133, PPAR-γ, α-SMA, CD31).
- In vitro differentiation assays to confirm multipotency (adipogenesis, osteogenesis, chondrogenesis).
- Immunohistochemistry to localize Hem-MSCs within the perivascular region of hemangioma tissue.
Main Results:
- Hem-MSCs were successfully isolated and exhibited fibroblast-like morphology.
- Hem-MSCs expressed standard MSC markers (CD105, CD90, CD29, vimentin) and CD133, PPAR-γ, PDGFR-β, and α-SMA.
- Hem-MSCs demonstrated in vitro differentiation into adipocytes, osteoblasts, and chondroblasts.
- Immunohistochemistry confirmed the perivascular localization of Hem-MSCs, co-expressing PDGFR-β/α-SMA, CD133/α-SMA, and PPAR-γ/α-SMA.
Conclusions:
- Mesenchymal stem cells can be isolated from proliferating infantile hemangiomas.
- These Hem-MSCs originate from the perivascular niche.
- The findings support the perivascular origin of MSCs in hemangioma and their potential role in tumor development and regression.
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