Review Article

Gingival Mesenchymal Stem/Progenitor Cells: A Unique Tissue Engineering Gem

Table 1

Human G-MSCs isolation protocols.

Protocol numberTissue culture methodStudy

(I)() Collected tissue incubated overnight with 2 mg/mL dispase at 4°C overnight to separate epithelium 
() The minced tissues are digested in 4 mg/mL collagenase IV for 2 h at 37°C 
(3) Cell filtered through 70 µm strainer 
() Cells seeded out  
() Single-cell cloning
[25]

(II)() Tissue mincing  
() Tissue digestion in 0.1% collagenase and 0.2% dispase for 15 min at 37°C
() Discarding of the first cell fraction containing some epithelial cells  
() Tissues are that further incubated with enzyme solution for 5, 10, and 15 min and all cell fractions that are pooled  
() Cells seeded out in tissue culture flasks
[18]

(III)() Tissues digested with 0.4% dispase for 30 min at 37°C followed by collagenase type I (0.66 mg/mL) for 50 min 
() Cell filtered through 70 µm strainer to single-cell suspensions 
() Single-cell cloning
[20]

(IV)() The minced tissues are digested in 3 mg/mL collagenase and 4 mg/mL dispase for 2 hours at 37°C 
() Cell filtered through 70 µm strainer 
() Single-cell suspension plated at a concentration of 60 cells/cm2
() Selection of single-cell-derived colonies
[23]

(V)() Tissue deepithelized under magnification and cut in small pieces (2 × 2 mm) and rinsed 
() Tissue placed in dry culture flasks to adhere for 30 min then medium slowly added 
() Flasks incubated for cells to grow out  
() STRO-1 magnetic cell sorting
[19]

(VI)() The minced tissues are digested in 2 mg/mL collagenase and 1 mg/mL dispase for 30 min  
() Discarding of the first cell fraction containing some epithelial cells  
() Tissues that are further incubated with same enzyme solution for 90 min at 37°C 
() Cell filtered through 70 µm strainer 
() Cells seeded out
[24]