TABLE 10.
Author | Classification | Intervention | Cell morphology | Cell viability (MTT‐Test) | Cell proliferation |
---|---|---|---|---|---|
Cuthbert 8 | Atrophic | Not applicable | Not applicable | Not applicable | Cells isolated from non‐union tissue behave similarly to that of BMA, readily forming colonies. CFU‐F from non‐union tissue were comparable to that of induced membrane tissue, indicating no difference in MSC content between the two tissues. |
El‐Jawhari 19 | Atrophic | MSC cultured in non‐union serum vs. union serum | Not applicable | Not applicable | Non‐union serum has negative effect on MSC proliferation (p = 0.031). |
Wang 10 | Not mentioned | Chordin, Noggin and Gremlin expression knockdown | Not applicable | The cell viability of MSCs remained unchanged with PSI. By contrast, the cell viability of PEI25 kDa‐treated MSCs dramatically dropped to 20% of the original value when the polymer concentration reached 15 μg/ml. | Not applicable |
Vallim 11 | Not mentioned | Non‐union MSCs, BM MSCs and osteoblasts were transplanted into the subcutaneous tissue of immunodeficient mice | Not applicable | Not applicable | Non‐union MSCs had proliferative and rates comparable to BM MSCs and osteoblasts. The percentage of cells staining positive for b‐galactosidase activity in non‐union MSCs cultures was comparable to those observed in BM MSCs and osteoblasts. |
Takahara 12 | Pseudoarthrosis | Not applicable | Fibroblast‐like spindle shape | Not applicable | Could be cultured through at least 10 passages, with minimal decline in their proliferative capacity |
Ismail 17 | Not mentioned | Not applicable | Not applicable |
Non‐union: viability of 87.1% (81.7%–90.8%); iliac crest: 89.8% (84.7%–94.5%). No differences were found between the two sources of MSCs (p = 0.175). |
Not applicable |
Abbreviations: BMA, bone marrow aspirate; BMP, bone morphogenic protein.