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Successful Introduction of Human Renovascular Units into the Mammalian Kidney.
Pleniceanu, Oren; Harari-Steinberg, Orit; Omer, Dorit; Gnatek, Yehudit; Lachmi, Bat-El; Cohen-Zontag, Osnat; Manevitz-Mendelson, Eugenia; Barzilai, Aviv; Yampolsky, Matan; Fuchs, Yaron; Rosenzweig, Barak; Eisner, Alon; Dotan, Zohar; Fine, Leon G; Dekel, Benjamin; Greenberger, Shoshana.
Afiliação
  • Pleniceanu O; The Pediatric Stem Cell Research Institute and Pediatric Nephrology Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Harari-Steinberg O; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Omer D; The Pediatric Stem Cell Research Institute and Pediatric Nephrology Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Gnatek Y; The Pediatric Stem Cell Research Institute and Pediatric Nephrology Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel binyamin.dekel@sheba.health.gov.il.
  • Lachmi BE; The Pediatric Stem Cell Research Institute and Pediatric Nephrology Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Cohen-Zontag O; The Pediatric Stem Cell Research Institute and Pediatric Nephrology Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Manevitz-Mendelson E; The Pediatric Stem Cell Research Institute and Pediatric Nephrology Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Barzilai A; Department of Dermatology, Sheba Medical Center, Tel Hashomer, Israel.
  • Yampolsky M; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Fuchs Y; Department of Dermatology, Sheba Medical Center, Tel Hashomer, Israel.
  • Rosenzweig B; Laboratory of Stem Cell Biology and Regenerative Medicine, Department of Biology, Technion-Israel Institute of Technology, Haifa, Israel.
  • Eisner A; Laboratory of Stem Cell Biology and Regenerative Medicine, Department of Biology, Technion-Israel Institute of Technology, Haifa, Israel.
  • Dotan Z; Department of Urology, Sheba Medical Center, Tel Hashomer, Israel.
  • Fine LG; Department of Urology, Sheba Medical Center, Tel Hashomer, Israel.
  • Dekel B; Department of Urology, Sheba Medical Center, Tel Hashomer, Israel.
  • Greenberger S; Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California.
J Am Soc Nephrol ; 31(12): 2757-2772, 2020 12.
Article em En | MEDLINE | ID: mdl-32753400
ABSTRACT

BACKGROUND:

Cell-based therapies aimed at replenishing renal parenchyma have been proposed as an approach for treating CKD. However, pathogenic mechanisms involved in CKD such as renal hypoxia result in loss of kidney function and limit engraftment and therapeutic effects of renal epithelial progenitors. Jointly administering vessel-forming cells (human mesenchymal stromal cells [MSCs] and endothelial colony-forming cells [ECFCs]) may potentially result in in vivo formation of vascular networks.

METHODS:

We administered renal tubule-forming cells derived from human adult and fetal kidneys (previously shown to exert a functional effect in CKD mice) into mice, alongside MSCs and ECFCs. We then assessed whether this would result in generation of "renovascular units" comprising both vessels and tubules with potential interaction.

RESULTS:

Directly injecting vessel-forming cells and renal tubule-forming cells into the subcutaneous and subrenal capsular space resulted in self-organization of donor-derived vascular networks that connected to host vasculature, alongside renal tubules comprising tubular epithelia of different nephron segments. Vessels derived from MSCs and ECFCs augmented in vivo tubulogenesis by the renal tubule-forming cells. In vitro coculture experiments showed that MSCs and ECFCs induced self-renewal and genes associated with mesenchymal-epithelial transition in renal tubule-forming cells, indicating paracrine effects. Notably, after renal injury, renal tubule-forming cells and vessel-forming cells infused into the renal artery did not penetrate the renal vascular network to generate vessels; only administering them into the kidney parenchyma resulted in similar generation of human renovascular units in vivo.

CONCLUSIONS:

Combined cell therapy of vessel-forming cells and renal tubule-forming cells aimed at alleviating renal hypoxia and enhancing tubulogenesis holds promise as the basis for new renal regenerative therapies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Endoteliais / Transplante de Células-Tronco Mesenquimais / Células-Tronco Mesenquimais / Glomérulos Renais / Túbulos Renais Limite: Animals / Humans Idioma: En Revista: J Am Soc Nephrol Assunto da revista: NEFROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Israel

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Endoteliais / Transplante de Células-Tronco Mesenquimais / Células-Tronco Mesenquimais / Glomérulos Renais / Túbulos Renais Limite: Animals / Humans Idioma: En Revista: J Am Soc Nephrol Assunto da revista: NEFROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Israel