Review
Copyright ©The Author(s) 2020.
World J Stem Cells. Oct 26, 2020; 12(10): 1080-1096
Published online Oct 26, 2020. doi: 10.4252/wjsc.v12.i10.1080
Table 2 Summary of urine-derived stem cell differentiation reports
Cell typeMediumSupplementsInitial densityProtocol durationNoteRef.
“MSC-like” differentiated cell types
Adipogenic cellsDMEMDexamethasone 1 µmol/L, isobutyl-1 methylxanthine 500 µmol/L, indomethacin 66 µmol/L, hydrocortisone 500 µmol/L14000 cells/cm²24 d2 d in DMEM without supplement before differentiation[15]
DMEM low glucoseDexamethasone 1 µmol/L, isobutyl-1 methylxanthine 500 µmol/L, indomethacin 100 µmol/L, insulin 10 µg/mL20000 cells/cm²28 d/[30]
Specific adipogenic mediumFBS (optional)1000 to 5000 cells/cm²14 d/[13,22,23,33,39]
Specific adipogenic mediumNA80% of confluency14 d/[24]
Chondrogenic cellsDMEM/Ham's F12Fetal calf serum 10%, insulin 6 µg/mL, ascorbic acid 2P 0.2 mmol/L, TGF-b1 10 ng/mL1500 cells/cm²28 d/[15]
Specific chondrogenic mediumNA50000 cells/cm²28 d/[22,24]
Specific chondrogenic mediumNA300000 cells to 1000000 cells28 dCell aggregation in conical polypropylene tube before differentiation[23]
Osteogenic cellsDMEM low glucoseDexamethasone 10-100 nmol/L, ascorbate2-phosphate 50-1500 µmol/L, glycerophosphate 10 mmol/L, FCS 10%, Vit D3 10 nmol/L (optional)1500 to 4000 cells/cm²28 d/[15,30]
DMEM low glucoseFBS + osteogenic supplement4000 cells/cm²28 d/[23]
Specific osteogenic mediumNA1000 cells/ cm²28 d/[39]
Specific osteogenic mediumNA80% confluency at P414 d to 21 d/[22,24,33]
Other cell types
Endothelial cellsEBM-2VEGF 50 ng/mL + FBS (optional)3000 to 5000 cells/cm²9 d to 14 dCoating with fibronectin + 2 d of preculture[23,31,32]
MicrobeadsVEGF1000 cells/cm²14 dMD[35]
Neuronal cellsSpecific nerve induction mediumNA6000 cells/cm²2 dPre-culture with DMEM + 20% FBS + 10 ng/mL bFGF 24 h[23]
DMEM F12hEGF 20 ng/mL, bFGF 40 ng/mL, B27 2%, NEAA 1%, l-glutamine 1%, insulin-transferrin-selenite 1%.20%-30% of confluency12 dCoating: Polystyrene[22]
NeuroCult NS-A differentiation kitNA100000 cells/cm²7 dPreculture[24]
NM3 basic neuronal induction mediumY27632 10 μmol/L, A8301 5 μmol/L, CHIR99021 3 μmol/L, TTNPB 1 μmol/L, forskolin5 μmol/L, valproic acid 0.5 mmol/L, sodium butyrate 0.1 mmol/LMDMDCoating with Matrigel and preculture (2 d)[37]
Skeletal myogenic cellsDMEMSkeletal supplement + SVF 10%, Horse serum 5%, hydrocortisone 50 µmol/L, dexamethasone 0,1 µmol/LMD28 d/[23]
Conditioned mediumNAMD28 d12 h of culture of medium with skeletal myogenic cells[23]
Conditioned mediumNA80% confluency14 dCulture of medium with skeletal myogenic cells[24]
Smooth muscle cellsDMEM + EFM (1:1)FBS, TGF-β1 (2.5 ng/mL), PDG-BB (2.5 to 5 ng/mL)1000 to 2000 cells/cm²14 d/[12,19,23,34,36]
Renal differentiation
PodocytesVRAD: DMEMF12FBS 10%, vitamin D3 100 nmol/L, retinoic acid 100 µmol/LMD48 hMD[14]
Tubular cellsREGMHepatocyte growth factor 50 ng/mLMD21 dMD[14]
Urothelium cellsKFSM + EFM (1:1)FBS 2%, EGF 30 ng/mL3000 cell/cm²14 dMD[36]
KFSMFBS 2%, EGF 30 ng/mL3000 cell/cm²14 dMD[34]
KFSM + EFM (4:1)FBS 2%, EGF 30 ng/mL3000 cells/cm²14 d/[36]
DMEM + KFSM (4:1)FBS 8%, EGF 30 ng/mL1,000 cells/cm²14 d/[19]
Conditioned medium from urothelial cells 8 h + EFM + KFSM (1:1)EGF 30 ng/mL50000 cells/cm²7 to 21 dDynamic culture[21]
Conditioned medium of smooth muscle cells 12 h + KFSM (1:1)NA50000 cells/cm²7 to 21 dDynamic culture[21]