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Table 2 Selected preclinical studies of MSCs-based tissue engineering for PFDs

From: MSC-based therapy in female pelvic floor disorders

Author/year

Animal/models

MSC sources

Materials

Implantation of the constructs

Tracking of MSCs

Main assessments

Main outcomes

Conclusions

Darzi et al. 2018 [86]

Mice/abdominal subcutaneous wound

Human eMSCs

Polyamide/gelatin composite mesh

Implanted into two pockets and sutured to the abdominal fascial layer

Transduced with a mCherry lentivirus

Immunofluorescence; ELISA; qPCR

Higher expression of M2 markers and reduced cytokines in eMSC/mesh; immunomodulatory effects were delayed and weaker in immunocompromised mice

The immune status affected the survival of xenogeneic eMSC which leads to differences in the short-term and long-term macrophage responses to implanted meshes

Ulrich et al. 2014 [78]

Rats/dorsal subcutaneous wound

Human eMSCs

Polyamide/gelatin mesh

Implanted into a subcutaneous pocket; two meshes inserted for each rat

Labeled with DiO

Histological analysis; immunofluorescence; uniaxial tensiometry

MSCs detected on the mesh up to 14 days; Meshes with MSCs promoted neovascularization and reduced leukocyte infiltration

Seeding with eMSC exerted an anti-inflammatory effect and promoted wound repair, and produced mesh with greater extensibility

Ding et al. 2018 [49]

Rats/posterior vaginal wall incision

Human UC-MSCs

PP mesh

Implanted into vaginal wall next to the rectovaginal fascia

Marked with GFP or RFP

Macroscopic evaluation; fluorescence microscopy; histological analysis

No difference in fibrotic remodeling and inflammatory cells number; a better vascularization in cell-seeded mesh and a thicker layer covered the cell-seeded scaffold

UC-MSCs with differentiated smooth muscle cells might have a potential role in fascia tissue engineering to repair POP in the future

Edwards et al. 2015 [85]

Rats/dorsal subcutaneous wound

Human eMSCs

Polyamide/gelatin mesh

Implanted into a subcutaneous pocket and secured to the muscle layer

/

Uniaxial biomechanical analysis; scanning electron microscopy

Cell-seeded scaffolds were significantly less stiff than non-cell-seeded scaffolds; Collagen growth and organization were enhanced in the long-term in cell-seeded scaffolds

Results suggest that neo-tissue formation and remodelling may be enhanced through seeding scaffolds with eMSCs

Paul et al. 2019 [46]

Rats/abdominal subcutaneous wound

Human eMSCs

3D printed PCL mesh

Implanted into a subcutaneous pocket with cell side facing abdominal wall

Transduced with a mCherry lentivirus

Scanning electron microscope; Atomic Force Microscopy; Fourier Transform Infrared Spectroscopy; histological analysis

eMSC printed on MES constructs promoted tissue integration, eMSC retention and an anti-inflammatory M2 macrophage phenotyp

eMSC bioprinting onto an MES mesh to produce a CAD-specific potentially surgical grade tissue engineered construct for possible urogynecological applications such as POP

  1. eMSCs endometrial MSCs, UC-MSCs umbilical cord-derived MSCs, PP polypropylene, PCL poly caprolactone, RFP red fluorescent protein, ELISA enzyme-linked immunosorbent assay, qPCR quantitative polymerase chain reaction