Figure 1From: Improving outcomes of acute kidney injury using mouse renal progenitor cells alone or in combination with erythropoietin or suraminCharacteristics and differentiation potency of MRPC. (A) Morphology of MRPC isolated from adult mouse kidney. Morphology of the cells after 1 passage (4 days), 8 passages, 25 passages, and 50 passages is shown by phase-contrast microscopy and immunofluorescence microscopy. After eight passages, the cells are monomorphic with a spindle-shape morphology, containing large nucleus and fluorescence. MRPC cultured to confluence at passage 25 do not overlay and maintain fluorescence. Autofluorescence was negligible in the control group. (magnification 200×) (B) Immunofluorescence microscopy of fluorescent MRPC (green) stained with the following antibodies (red): anti-Oct-4 antibodies, anti-Pax-2 antibodies, an anti-alpha smooth muscle actin antibody (α-SMA), an anti-vimentin antibody, an anti-E-cadherin antibody and secondary antibody only (magnification 400×). (C) Gene expression of mMSC (bone marrow) and MRPC detected by RT-PCR. (D) Mutilineage differentiation of MRPC. Phase-contrast microscopy and immunofluorescence microscopy of MRPC that were incubated under culture conditions that induced differentiation into osteoblasts and adipocytes. Control A was osteogenic differentiation and control B was adipogenic differentiation (magnification 100×). MRPC, mouse renal progenitor cells; MSC, mesenchymal stem cells, α-SMA.Back to article page