Table 1.
| Author, reference, year |
Cell Type | Biological Source | Model/Biological Effect |
|---|---|---|---|
| Patschan et al100 2006 | Pro-angiogenic | Murine spleen and kidney | Unilateral I/R in FVB/NJ and Tie-2-GFP mice |
| Reduced plasma creatinine by ~50% post I/R | |||
| No evidence of homing | |||
|
| |||
| Patschan et al101 2010 | Pro-angiogenic | Murine peripheral blood, spleen and bone marrow | Unilateral I/R in male C57BL/6N mice |
| Reduced plasma creatinine by ~40–75% post-I/R | |||
| Reduced plasma creatinine by ~90% post-I/R with Epac-1 Ac pretreatment | |||
| Evidence of minimal homing | |||
|
| |||
| Patschan et al121 2012 | Murine peripheral blood and spleen | Similar models as above; pretreatment of cells with melatonin, Angiopoietin-1 and BMP-5 enhances protective response, with minimal homing | |
| Patschan et al122 2013 | |||
| Patschan et al123 2013 | |||
|
| |||
| Patschan et al124 2015 | Pro-angiogenic | Murine peripheral blood and spleen | Bilateral I/R in male C57BL/6N mice, reduced plasma creatinine, increased endothelial autophagy and decreased |
| Patschan et al442016 | EndoMT and attenuated capillary rarefaction | ||
|
| |||
| Burger et al1122015 | ECFC & ECFC exosomes | Human umbilical cord | Bilateral I/R in male NOD-SCID mice |
| Reduced plasma creatinine by ~40% post-I/R | |||
| Improved tubular morphology | |||
| No evidence of homing | |||
|
| |||
| Collett et al192017 | ECFC | Rat PMVEC and human ECFC-conditioned media | Bilateral I/R in male Sprague Dawley rats |
| Reduced plasma creatinine by ~50% post-I/R | |||
| Improved tubular morphology | |||
| Prevented loss of medullary blood flow | |||
| No evidence of homing | |||
|
| |||
| Viñas et al91 2016 | ECFC | Human umbilical cord blood ECFC derived exosomes | Bilateral I/R in male FVB mice |
| Reduced plasma creatinine by ~90% post-I/R | |||
| Improved tubular morphology | |||
|
| |||
| Brodsky et al111 2001 | EC | Human umbilical cord | Unilateral I/R in male Athymic rats |
| Reduced plasma creatinine by ~50% post-I/R | |||
| Maintained microvascular perfusion | |||
| Evidence of minimal homing | |||
|
| |||
| Cantaluppi et al115 2012 | ECFC derived microvesicles | Human peripheral blood | Unilateral I/R in male Wistar rats |
| Reduced plasma creatinine by ~80% post-I/R | |||
| Improved tubular morphology | |||
| Prevented capillary rarefaction | |||
|
| |||
| Liang et al125 2015 | EC | Human Umbilical cords (Wharton’s Jelly) | Unilateral I/R in male C57BL/6 mice |
| Reduced plasma creatinine by ~70% post-I/R | |||
| Improved tubular morphology | |||
| Potential prevention of capillary rarefaction | |||
| Evidence of minimal homing | |||
|
| |||
| Pang et al113 2017 | EC or ECFC | Human renal artery | Bilateral I/R and nephron mass reduction in NOD-SCID mice. Reduced plasma creatinine by ~50% post-I/R |
| Prevented capillary rarefaction | |||
| Minimal homing near peritubular capillaries up to 10 days | |||
|
| |||
| Patschan et al114 2017 | Indeterminate | Murine peripheral blood and spleen | Bilateral I/R in male C57BL/6 mice |
| Reduced plasma creatinine by ~10% at 1 week, did not prevent capillary rarefaction | |||
|
| |||
| Zullo et al126 2015 | Indeterminate | Murine embryonic EPC line cultured with MSCs | Improved renal function, medullary RBF and increased M1 to M2 macrophage polarization in LPS induced endoxemia in C57BL6 mice. |
ECFC-endothelial colony forming cells; EC-endothelial cells