From: Tumor-initiating and metastasis-initiating cells of clear-cell renal cell carcinoma
Studies | Approaches | Markers | Other markers | Negative expression | Location/cell type | Property and function | Other characteristics | Reference |
---|---|---|---|---|---|---|---|---|
1 | Label (BrdU)-retaining cells in rat kidney | Â | Â | Â | PT and DT; thick ascending LOH; CD | Proliferation after injury in vivo | Â | Maeshima et al. [120] |
2 | Label (BrdU)-retaining cells in rat and mouse kidneys | Â | Â | Â | Renal papilla | Multipotency in vitro; sphere formation; proliferation after injury; incorporate into parenchyma after injection into renal cortex | Scattered LRCs also found in outer cortex and medulla | Oliver et al. [121] |
3 | Limiting dilution for proliferative mouse kidney cells | Sox9 (used for lineage tracing) | CD133, Lgr4, Foxd1, Pax8, Notch (Hey1, Hes1, Hes5) and Wnt (Axin) target genes | Lgr5, Pax2, Six2, Scf, c-Kit, CD90, and CD105 | PT and DT | Populate PT, LOH, and DT in embryo and after injury in adult (but not glomeruli or CD) |  | Kang et al. [122] |
4 | Limiting dilution and growth of dissected rat kidney S3 segment | Â | Sca1, c-Kit, c-Met, Vimentin, Wnt4, WT-1 Pax2 | Â | S3 segment of the proximal tubule in rat kidney | Form tubule structure after implantation; regenerate tubules after drug-induced injury | Differentiate into tubule cells expressing multiple segmental markers | Kitamura et al. [123] |
5 | Serial passages of cultured whole adult rat kidney suspension | Oct4 (used for lineage tracing) | Pax2, CD90, CD44, Vimentin | SSEA-1, CD133, CD106, CD31 | PT in the cortical medullary junction | Multipotency in vitro; incorporate into PT and DT (but not LOH) after injection into injured kidney | Â | Gupta et al. [124] |
6 | Outgrowth of cultured capsulated glomeruli in vitro followed by sorting | CD133+ CD24+, CD106+ (used for sorting) | CK7 and Vimentin | Â | Urinary pole of Bowman's capsule | Proliferate and differentiate into podocyte and tubular lineages in vitro; regenerate podocytes and tubular cells in SCID post-injuries | Â | Angelotti et al. [74] |
7 | Outgrowth of cultured renal tubules in vitro followed by sorting | CD133+, CD24+, CD106− (used for sorting) | CK7 and Vimentin |  | PT, DT | Proliferate and differentiate into tubular lineage in vitro; regenerate tubular cells in SCID post-injuries |  | Angelotti et al. [74] |
8 | Outgrowth of cultured human glomeruli in vitro followed by sorting | CD133, CD24 (used for sorting) | CD106, CD105, CD54, and CD44 |  | Urinary pole of Bowman's capsule | Self-renewal; clonogenic potential; multilineage differentiation; repopulate glomeruli, PT, and DT in SCID mice after injury | • Differentiate into tubule cells expressing multiple segmental markers simultaneously in vitro | Sagrinati et al. [75] |
9 | Side population of adult mouse whole kidney cells after Hoechst 33342 staining | CD24a (used for localizing SP cells in vivo) | Sca1, CD105, CD44, Pax8, Notch1/2 | CD45, CD34, and c-Kit (positive for SP from bone marrow) | Mostly in PT, also in DT, thick ascending LOH, CD | Multipotency in vitro; incorporate into explant of developing MM and UB; engraft into PT, DT, and CD of injured adult kidney | Â | Challen et al. [125] |
10 | Magnetic bead sorting of human adult renal papilla suspension, followed by colony formation in culture | CD133 | OCT4, CD73, CD29, CD44, CD146, SSEA-4, ZO-1, cytokeratin, Vimentin, Nestin, PAX2 OCT4, c-MYC, KLF4 | CD34, CD90, CD117, CD45 | Papilla, LOH thin limb segments | Differentiate into tubule cell fates of all segments in vitro; incorporate into different tubule segments after injection into SCID mice | Â | Bussolati et al. [73] Bussolati et al. [184] |
11 | MSCs isolated from adult mouse kidney; sorting for Lin−CD31− CD24lo Sca-1+; sorting for Hob7-driven GFP+ cells; lineage tracing | CD24lo Sca-1+ | Hoxb7, Wnt4, BNP, Uroplakin 1b, Aqp2 (principal cell marker) | F4/80 (macrophage marker), UMOD; CD31; Pendrin or AE1 (intercalated cell markers); PDGFRα and β (pericyte markers) | CD (principal cells) | Display EMT after in vitro culture; exhibit MSC-like property; integrate into Aqp 2-positive medullary CD when injected into neonatal kidneys; form epithelial structures in vitro and in vivo | May originate from interstitial Wnt4-expressing cells integrated into CD after birth; able to produce growth factors that promote epithelial wound repair in vitro | Li et al. [127] |
12 | scRNAseq of human urine cells | SOX9 (used as marker in selection for serial enrichment) | SOX4, HES1, TLE4 | Â | Un-specified tubular cells | Serial culture enrichment for SOX9+; incorporate into incised SCID mouse kidney | Â | Wang et al. 2021 [128] |