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Table 1 Differences between BMSCs and ASCs in co-culture with ECs

From: Vascularization mediated by mesenchymal stem cells from bone marrow and adipose tissue: a comparison

 

BMSCs

ASCs

3D matrix used for co-culture

Fibrin [9, 38, 39, 42, 43, 49], polyurethane [37], type I collagen [38], fibrin + type I collagen in different ratios [38]

Fibrin [9, 33, 43, 51, 52]

Pericytic marker

α-SMA [9, 37, 46], NG2 [37], CD146 [37]

α-SMA [9, 50], NG2 [33]

Paracrine factors

HGF, TIMP1, TIMP2 [9]

HGF, TNF-α [51], PD-ECGF, FGF-2, MMP-9, Ang-2, pentraxin-3 [33], ECM proteins: collagen IV, fibronectin [50]

Altered gene expression

FGF-2 ↑, TGFB1 ↑, VEGFA ↑ [42], vWF ↑, CD31 ↑, VE-cadherin ↑, angiopoietin-related protein 4 ↑, CD34 ↑, CD93 ↑, CDH5 ↑ [45], MMPs ↑ [39]

CD31 ↑, VE-cadherin ↑, VEGFR-2 ↑, vWF ↑ [33]

Endothelial cell type

HUVECs [9, 37–39, 43, 45, 46, 48, 49],EPCs [37], ECFCs [42]

HUVECs [9, 33, 43, 51], OECs [33, 52]

MMPs important for network formation and ECM degradation

Yes (in contrast to fibroblasts) [39, 49]

Yes [52], to a lesser extent as plasmin family proteases [51]

  1. BMSCs and ASCs have different effects on ECs and show altered behavior concerning pericytic marker expression, paracrine factors, gene expression, and importance of MMPs for network formation. Furthermore, different matrices as well as different EC types were used to investigate effects of MSCs on ECs