Percutaneous intrarenal transplantation of differentiated induced pluripotent stem cells into newborn mice.


Journal

Anatomical record (Hoboken, N.J. : 2007)
ISSN: 1932-8494
Titre abrégé: Anat Rec (Hoboken)
Pays: United States
ID NLM: 101292775

Informations de publication

Date de publication:
10 2020
Historique:
received: 06 08 2019
revised: 22 11 2019
accepted: 07 12 2019
pubmed: 13 2 2020
medline: 10 4 2021
entrez: 13 2 2020
Statut: ppublish

Résumé

The in vivo engraftment of induced pluripotent stem cell (iPSC)-derived podocytes following allogeneic transplantation into host kidneys remains a challenge. Here we investigate the survival and engraftment of human dermal fibroblasts-derived differentiated iPSCs using a newborn mouse model, which represents a receptive immunoprivileged host environment. iPSCs were generated from skin biopsies of patients using Sendai virus reprogramming. Differentiation of nephrin (NPHS1)-green fluorescent protein (GFP) iPSCs into kidney podocytes (iPSC-PODs) was performed by the addition of Activin A, bone morphogenetic protein 7 (BMP7), and retinoic acid over 10 days of culture. To assess the in vivo incorporation of cells, undifferentiated iPSCs or day 10 iPSC-PODs, were labeled with either carboxyfluorescein succinimidyl ester (CFSE) or Qdot nanocrystals (Q705). Thereafter, 1 × 10

Identifiants

pubmed: 32048472
doi: 10.1002/ar.24371
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2603-2612

Informations de copyright

© 2020 American Association for Anatomy.

Références

Afkarian, M., Sachs, M. C., Kestenbaum, B., Hirsch, I. B., Tuttle, K. R., Himmelfarb, J., & de Boer, I. H. (2013). Kidney disease and increased mortality risk in type 2 diabetes. Journal of the American Society of Nephrology, 24(2), 302-308. https://doi.org/10.1681/ASN.2012070718
Bantounas, I., Ranjzad, P., Tengku, F., Silajdžić, E., Forster, D., Asselin, M.-C., … Wang, Q. (2018). Generation of functioning nephrons by implanting human pluripotent stem cell-derived kidney progenitors. Stem Cell Reports, 10(3), 766-779.
Bartolomucci, A., Gioiosa, L., Chirieleison, A., Ceresini, G., Parmigiani, S., & Palanza, P. (2004). Cross fostering in mice: Behavioral and physiological carry-over effects in adulthood. Genes, Brain and Behavior, 3(2), 115-122.
Behr, L., Hekmati, M., Lucchini, A., Houcinet, K., Faussat, A. M., Borenstein, N., … Laborde, K. (2009). Evaluation of the effect of autologous mesenchymal stem cell injection in a large-animal model of bilateral kidney ischaemia reperfusion injury. Cell Proliferation, 42(3), 284-297. https://doi.org/10.1111/j.1365-2184.2009.00591.x
Davies, J. A., & Lawrence, M. L. (2018). Chapter 14-four challenges for organoid engineers. In J. A. Davies & M. L. Lawrence (Eds.), Organs and Organoids (pp. 255-259). Elsevier Inc., Netherlands.
Dekel, B., Amariglio, N., Kaminski, N., Schwartz, A., Goshen, E., Arditti, F. D., … Rechavi, G. (2002). Engraftment and differentiation of human metanephroi into functional mature nephrons after transplantation into mice is accompanied by a profile of gene expression similar to normal human kidney development. Journal of the American Society of Nephrology, 13(4), 977-990.
Freedman, B. S., Brooks, C. R., Lam, A. Q., Fu, H., Morizane, R., Agrawal, V., … Bonventre, J. V. (2015). Modelling kidney disease with CRISPR-mutant kidney organoids derived from human pluripotent epiblast spheroids. Nature Communications, 6, 8715. https://doi.org/10.1038/ncomms9715
Garreta, E., Sanchez, S., Lajara, J., Montserrat, N., & Belmonte, J. C. I. (2018). Roadblocks in the path of iPSC to the clinic. Current Transplantation Reports, 5(1), 14-18.
Guo, J. K., Marlier, A., Shi, H., Shan, A., Ardito, T. A., Du, Z. P., … Cantley, L. G. (2012). Increased tubular proliferation as an adaptive response to glomerular albuminuria. Journal of the American Society of Nephrology, 23(3), 429-437. https://doi.org/10.1681/asn.2011040396
Harari-Steinberg, O., Pleniceanu, O., & Dekel, B. (2011). Selecting the optimal cell for kidney regeneration: Fetal, adult or reprogrammed stem cells. Organogenesis, 7(2), 123-134. https://doi.org/10.4161/org.7.2.15783
Hartman, H. A., Lai, H. L., & Patterson, L. T. (2007). Cessation of renal morphogenesis in mice. Developmental Biology, 310(2), 379-387. https://doi.org/10.1016/j.ydbio.2007.08.021
Huber, T. B., Kottgen, M., Schilling, B., Walz, G., & Benzing, T. (2001). Interaction with podocin facilitates nephrin signaling. The Journal of Biological Chemistry, 276(45), 41543-41546. https://doi.org/10.1074/jbc.C100452200
Imberti, B., Tomasoni, S., Ciampi, O., Pezzotta, A., Derosas, M., Xinaris, C., … Benigni, A. (2015). Renal progenitors derived from human iPSCs engraft and restore function in a mouse model of acute kidney injury. Scientific Reports, 5, 8826.
Kunter, U., Rong, S., Djuric, Z., Boor, P., Müller-Newen, G., Yu, D., & Floege, J. (2006). Transplanted mesenchymal stem cells accelerate glomerular healing in experimental glomerulonephritis. Journal of the American Society of Nephrology, 17(8), 2202-2212. https://doi.org/10.1681/asn.2005080815
Lam, A. Q., Freedman, B. S., & Bonventre, J. V. (2014). Directed differentiation of pluripotent stem cells to kidney cells. Paper presented at the Seminars in nephrology.
Little, M. H., Hale, L. J., Howden, S. E., & Kumar, S. V. (2019). Generating kidney from stem cells. Annual Review of Physiology, 81, 335-357.
McFetridge, M. L., Del Borgo, M. P., Aguilar, M.-I., & Ricardo, S. D. (2018). The use of hydrogels for cell-based treatment of chronic kidney disease. Clinical Science, 132(17), 1977-1994.
Moghadasali, R., Azarnia, M., Hajinasrollah, M., Arghani, H., Nassiri, S. M., Molazem, M., … Aghdami, N. (2014). Intra-renal arterial injection of autologous bone marrow mesenchymal stromal cells ameliorates cisplatin-induced acute kidney injury in a rhesus macaque mulatta monkey model. Cytotherapy, 16(6), 734-749. https://doi.org/10.1016/j.jcyt.2014.01.004
Morizane, R., Lam, A. Q., Freedman, B. S., Kishi, S., Valerius, M. T., & Bonventre, J. V. (2015). Nephron organoids derived from human pluripotent stem cells model kidney development and injury. Nature Biotechnology, 33(11), 1193-1200. https://doi.org/10.1038/nbt.3392
Musah, S., Mammoto, A., Ferrante, T. C., Jeanty, S. S. F., Hirano-Kobayashi, M., Mammoto, T., … Ingber, D. E. (2017). Mature induced-pluripotent-stem-cell-derived human podocytes reconstitute kidney glomerular-capillary-wall function on a chip. Nature Biomedical Engineering, 1. https://doi.org/10.1038/s41551-017-0069
Peired, A. J., Sisti, A., & Romagnani, P. (2016). Mesenchymal stem cell-based therapy for kidney disease: A review of clinical evidence. Stem Cells International, 2016, 4798639-4798622. https://doi.org/10.1155/2016/4798639
Picollet-D'hahan, N., Dolega, M. E., Freida, D., Martin, D. K., & Gidrol, X. (2017). Deciphering cell intrinsic properties: A key issue for robust organoid production. Trends in Biotechnology, 35(11), 1035-1048.
Pleniceanu, O., Harari-Steinberg, O., & Dekel, B. (2010). Concise review: Kidney stem/progenitor cells: Differentiate, sort out, or reprogram? Stem Cells, 28(9), 1649-1660.
Pozzi, A., Jarad, G., Moeckel, G. W., Coffa, S., Zhang, X., Gewin, L., … Zent, R. (2008). Beta1 integrin expression by podocytes is required to maintain glomerular structural integrity. Developmental Biology, 316(2), 288-301. https://doi.org/10.1016/j.ydbio.2008.01.022
Quimby, J. M., Webb, T. L., Randall, E., Marolf, A., Valdes-Martinez, A., & Dow, S. W. (2016). Assessment of intravenous adipose-derived allogeneic mesenchymal stem cells for the treatment of feline chronic kidney disease: A randomized, placebo-controlled clinical trial in eight cats. Journal of Feline Medicine and Surgery, 18(2), 165-171. https://doi.org/10.1177/1098612x15576980
Reiser, J., Kriz, W., Kretzler, M., & Mundel, P. (2000). The glomerular slit diaphragm is a modified adherens junction. Journal of the American Society of Nephrology, 11(1), 1-8.
Saleem, M. A., O'Hare, M. J., Reiser, J., Coward, R. J., Inward, C. D., Farren, T., … Mundel, P. (2002). A conditionally immortalized human podocyte cell line demonstrating nephrin and podocin expression. Journal of the American Society of Nephrology, 13(3), 630-638.
Sharmin, S., Taguchi, A., Kaku, Y., Yoshimura, Y., Ohmori, T., Sakuma, T., … Nishinakamura, R. (2016). Human induced pluripotent stem cell-derived podocytes mature into vascularized glomeruli upon experimental transplantation. Journal of the American Society of Nephrology, 27(6), 1778-1791.
Short, K. M., Combes, A. N., Lefevre, J., Ju, A. L., Georgas, K. M., Lamberton, T., … Little, M. H. (2014). Global quantification of tissue dynamics in the developing mouse kidney. Developmental Cell, 29(2), 188-202. https://doi.org/10.1016/j.devcel.2014.02.017
Song, B., Smink, A. M., Jones, C. V., Callaghan, J. M., Firth, S. D., Bernard, C. A., … Ricardo, S. D. (2012). The directed differentiation of human iPS cells into kidney podocytes. PLoS One, 7(9), e46453.
Taguchi, A., & Nishinakamura, R. (2015). Nephron reconstitution from pluripotent stem cells. Kidney International, 87(5), 894-900.
Taguchi, A., & Nishinakamura, R. (2017). Higher-order kidney organogenesis from pluripotent stem cells. Cell Stem Cell, 21(6), 730-746.e736. https://doi.org/10.1016/j.stem.2017.10.011
Takahashi, K., Tanabe, K., Ohnuki, M., Narita, M., Ichisaka, T., Tomoda, K., & Yamanaka, S. (2007). Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell, 131(5), 861-872.
Takasato, M., Er, P. X., Chiu, H. S., Maier, B., Baillie, G. J., Ferguson, C., … Little, M. H. (2015). Kidney organoids from human iPS cells contain multiple lineages and model human nephrogenesis. Nature, 526(7574), 564-568. https://doi.org/10.1038/nature15695
Toyohara, T., Mae, S.-I., Sueta, S.-I., Inoue, T., Yamagishi, Y., Kawamoto, T., … Tanaka, H. (2015). Cell therapy using human induced pluripotent stem cell-derived renal progenitors ameliorates acute kidney injury in mice. Stem Cells Translational Medicine, 4(9), 980-992.
Turner, P. V., Brabb, T., Pekow, C., & Vasbinder, M. A. (2011). Administration of substances to laboratory animals: Routes of administration and factors to consider. Journal of the American Association for Laboratory Animal Science: JAALAS, 50(5), 600-613.
van den Berg, C. W., Ritsma, L., Avramut, M. C., Wiersma, L. E., van den Berg, B. M., Leuning, D. G., … Koster, A. J. (2018). Renal subcapsular transplantation of PSC-derived kidney organoids induces neo-vasculogenesis and significant glomerular and tubular maturation in vivo. Stem Cell Reports, 10(3), 751-765.
Weber, E. M., Algers, B., Hultgren, J., & Olsson, I. A. S. (2013). Pup mortality in laboratory mice-infanticide or not? Acta Veterinaria Scandinavica, 55(1), 83-83. https://doi.org/10.1186/1751-0147-55-83

Auteurs

Ricky W K Lau (RWK)

Department of Anatomy and Developmental Biology, Biomedical Discovery Institute, Monash University, Clayton, Victoria, Australia.

Ali Al-Rubaie (A)

Department of Anatomy and Developmental Biology, Biomedical Discovery Institute, Monash University, Clayton, Victoria, Australia.

Sheetal Saini (S)

Department of Anatomy and Developmental Biology, Biomedical Discovery Institute, Monash University, Clayton, Victoria, Australia.

Andrea F Wise (AF)

Department of Anatomy and Developmental Biology, Biomedical Discovery Institute, Monash University, Clayton, Victoria, Australia.

Sharon D Ricardo (SD)

Department of Anatomy and Developmental Biology, Biomedical Discovery Institute, Monash University, Clayton, Victoria, Australia.

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