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. 2022 Oct 9;9:103. doi: 10.1186/s40634-022-00537-0

Table 4.

Immuno-phenotypic analysis performed and CD Marker Expression

Device/ System used
(Author)
Type of immuno-phenotypic analysis of cell subtypes Terminology for uncultured, freshly isolated cells Stage of cell processing Positive cell CD marker expression (%)
Mesenchymal stem cell markers
*CD markers observed in Pericytes as well
Endothelial cell, pericyte and haematopoetic markers
CD 13 CD 29 CD 44* CD 73 CD 90* CD 105* CD 146* CD 31 CD 34 CD 45 CD 68 Other
Adinizer (Copcu et al. [18]) Flow Cytometry Stromal cells/ Nuclear cells Immediately after device use (minimally manipulated) As per methods- Proportions of CD45 negative cells were analysed in CD34−CD146+ and CD34+CD146−CD90+ (deemed as regenerative perivascular cells), and CD34+CD146+ as endothelial cells. However, percentages not specifically reported in results.
No control
Passage in culture following device (extensively manipulated)
Adiprep (Dragoo et al. [27]) Flow Cytometry SVF Cells Immediately after device use (minimally manipulated) 56.5 72.0 60.4 65.2 33.4 80.3
No control
Passage in culture following device (extensively manipulated) 94.3 96.6 97.0
Fastem (Domenis et al. [24]) Flow Cytometry SVF Cells Immediately after device use (minimally manipulated) 50-60

CD34+CD45-CD31-

10-20

Control- ‘modified’ Coleman’s procedure (centrifugation) 0-10

CD34+CD45-CD31-

20-30

Passage in culture following device (extensively manipulated)
Fastem and MyStem (Gentile et al. [29]) Not done SVF Nucleated Cells
Hy-Tissue SVF (Busato et al. [12]) Flow Cytometry Free nucleated SVF cells Immediately after device use (minimally manipulated) 7.61 6.28 2.6 9.91 5.5 3.5 CD116 0.7
Control- enzymatic digestion using 0.1% collagenase type I at 37 °C for 45min followed by centrifugation at 400G for 10min. 10.1 9.98 3.67
Passage in culture following device (extensively manipulated) 90 >90 >70 60 90
Lipocube Nano (Cohen et al. [17]) Flow Cytometry SVF Cells Immediately after device use (minimally manipulated) 42.0 53 55.8 53.2 18.8
No control
Passage in culture following device (extensively manipulated)
Lipocube SVF (Tiryaki et al. [66]) Flow Cytometry Nucleated SVF Cells Immediately after device use (minimally manipulated) 21.5 6.16 11.4 9.0
Control- enzymatic digestion using GMP grade collagenase NB6 at a concentration of 0.1 U/ml at 37 °C for 30min followed by centrifugation at 400G for 10min. Then washed with PBS solution and centrifuged at 300G for 5min. 6.93 3.44 5.88 3.06
Passage in culture following device (extensively manipulated)
Lipogems (Vezzani et al. [75]) Flow Cytometry SVF Nucleated Cells Immediately after device use (minimally manipulated)

CD146+CD34 33.5

CD34+CD146 5.46

No control

CD146+CD34 8.39

CD34+CD146 51.5

Passage in culture following device (extensively manipulated) CD14, CD31, CD40 ligand (CD154) significantly more abundant than when compared to control.
Lull pgm (Morselli et al. [42]) Not done SVF Cells
MyStem (Cicione et al. [16]) Flow Cytometry Lipoaspirate fluid cells Immediately after device use (minimally manipulated) <0.1 1-1.5 <0.1 0.5-1 <0.5 <1
Control- centrifugation ‘as previously described’ <0.1 1.5-2 <0.1 1 <0.5 <0.5
Passage in culture following device (extensively manipulated) 93 98 95 96
MyStem (Tarallo et al. [65]) Flow Cytometry Freshly isolated LAF Cells Immediately after device use (minimally manipulated) 0-10 75 0-10 0-10 20 CD31 30
No control
Passage in culture following device (extensively manipulated) All culture-expanded cells displayed an ASC-like immunophenotype: CD105+, CD73+, CD90+, CD45- and CD34-CD31.
Puregraft (Streit et al. [63]) Direct Immunofluorescence SVF Cells Immediately after device use (minimally manipulated)

Analysed adhesive properties to determine stem cell nature.

All adherent cells were positive for CD90 and CD105 and negative for CD31 and CD45 antigens (stem cell marker). Numbers not specified.

Control 1- aliquot was left at 37°C for 20min under the action of gravity (decantation).

Control 2- aliquot centrifuged at 1200G for 3 min.

Passage in culture following device (extensively manipulated)
Rigenera (Dai Pre et al. [20]) Flow Cytometry Total cells Immediately after device use (minimally manipulated) 3.12 4.98

CD44/CD90 30.4

CD73/CD105 16.6

CD73/29 27.8

Control- enzymatic digestion using 0.1% collagenase type I at 37 °C for 45min in Hank’s Balanced Salt Solution (HBSS) and 2% bovine serum albumin followed by centrifugation at 3000 rpm for 7min. 76.7 7.32

CD44/CD90 48.1

CD73/CD105 54.3

CD73/29 62

Passage in culture following device (extensively manipulated) Expression of the typical mesenchymal stem cell markers (CD105, CD90, CD73, CD44, and CD29) and the hematopoietic markers (CD45 and CD34) was preserved through culture passages.
Transpose RT (Winnier et al. [77]) Not done Adipose-derived regenerative cells
Tulip Nanotransfer (Cohen et al. [17]) Flow Cytometry SVF Cells Immediately after device use (minimally manipulated) 18.3 50 42.1 24.1 7.9
No control
Passage in culture following device (extensively manipulated)
Tulip Nanotransfer (Sese et al. [61]) Not done Nanofat cells