| CPC A61K 35/22 (2013.01) [C12N 5/0081 (2013.01); C12N 5/0686 (2013.01); G01N 33/56966 (2013.01); C12N 2500/02 (2013.01); C12N 2501/58 (2013.01); C12N 2501/599 (2013.01); G01N 2333/4742 (2013.01); G01N 2333/705 (2013.01); G01N 2333/9108 (2013.01)] | 19 Claims |
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1. A method for preparing a formulation for treatment of kidney disease in a mammal comprising:
characterizing a heterogeneous renal cell population prepared from a kidney sample of the mammal as suitable for implantation and/or eliciting a regenerative response, the characterizing comprising:
(i) determining that cells of the population express gamma-glutamyl transpeptidase (GGT)-1;
(ii) determining that cells of the population express a cytokine cytokeratin (CK); and
(iii) determining that cells of the population secrete vascular endothelial growth factor (VEGF) and kidney injury molecule (KIM)-1; and
formulating the heterogeneous renal cell population, characterized as suitable for implantation and/or eliciting the regenerative response, with a (i) biomaterial or (ii) pharmaceutically acceptable carrier or excipient.
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