Cellular interactions via conditioned media induce in vivo nephron generation from tubular epithelial cells or mesenchymal stem cells

• Published in: Biochemical and biophysical research communications 2013-06, Vol.435 (3), p.327-333
• Main Authors: Machiguchi, Toshihiko, Nakamura, Tatsuo
• Format: Article
• Language: English
• Subjects: 60 APPLIED LIFE SCIENCES; ANIMAL TISSUES; Animals; BUDS; Cell Communication - physiology; Cell Differentiation; CELL PROLIFERATION; Cells, Cultured; Conditioned medium; Cross-talk; Culture Media, Conditioned; Cytokines - metabolism; Dogs; Endothelial Cells - cytology; Endothelial Cells - physiology; Epithelial Cells - cytology; Epithelial Cells - physiology; Glomerulogenesis; Humans; IN VIVO; Kidney Tubules - cytology; Kidney Tubules - physiology; KIDNEYS; Mesenchymal stem cell; Mesenchymal Stem Cell Transplantation; Mesenchymal Stromal Cells - cytology; Mesenchymal Stromal Cells - physiology; Mice; MORPHOLOGICAL CHANGES; Nephron generation; Nephrons - cytology; Nephrons - physiology; Rats; Rats, Hairless; Regeneration - physiology; STEM CELLS; Transplantation, Heterologous; Tubular epithelial cell
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2013.04.050

•We have attempted in vivo nephron generation using conditioned media.•Vascular and tubular cells do cross-talks on cell proliferation and tubular changes.•Tubular cells suppress these changes in mesenchymal stem cells.•Tubular cells differentiate mesenchymal stem cells into tubular cells.•Nephrons can be created from implanted tubular cells or mesenchymal stem cells. There are some successful reports of kidney generation by utilizing the natural course of kidney development, namely, the use of an artificially treated metanephros, blastocyst or ureteric bud. Under a novel concept of cellular interactions via conditioned media (CMs), we have attempted in vivo nephron generation from tubular epithelial cells (TECs) or mesenchymal stem cells (MSCs). Here we used 10× CMs of vascular endothelial cells (VECs) and TECs, which is the first to introduce a CM into the field of organ regeneration. We first present stimulative cross-talks induced by these CMs between VECs and TECs on cell proliferation and morphological changes. In MSCs, TEC-CM suppressed these changes, however, induced cytokeratin expression, indicating the differentiation of MSCs into TECs. As a result, glomerular and tubular structures were created following the implantation of TECs or MSCs with both CMs. Our findings suggest that the cellular interactions via CMs might induce in vivo nephron generation from TECs or MSCs. As a promoting factor, CMs could also be applied to the regeneration of other organs and tissues.