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A tissue-bioengineering strategy for modeling rare human kidney diseases in vivo.

Nature communications (2021-11-13)
J O R Hernandez, X Wang, M Vazquez-Segoviano, M Lopez-Marfil, M F Sobral-Reyes, A Moran-Horowich, M Sundberg, D O Lopez-Cantu, C K Probst, G U Ruiz-Esparza, K Giannikou, R Abdi, E P Henske, D J Kwiatkowski, M Sahin, D R Lemos
RESUMEN

The lack of animal models for some human diseases precludes our understanding of disease mechanisms and our ability to test prospective therapies in vivo. Generation of kidney organoids from Tuberous Sclerosis Complex (TSC) patient-derived-hiPSCs allows us to recapitulate a rare kidney tumor called angiomyolipoma (AML). Organoids derived from TSC2-/- hiPSCs but not from isogenic TSC2+/- or TSC2+/+ hiPSCs share a common transcriptional signature and a myomelanocytic cell phenotype with kidney AMLs, and develop epithelial cysts, replicating two major TSC-associated kidney lesions driven by genetic mechanisms that cannot be consistently recapitulated with transgenic mice. Transplantation of multiple TSC2-/- renal organoids into the kidneys of immunodeficient rats allows us to model AML in vivo for the study of tumor mechanisms, and to test the efficacy of rapamycin-loaded nanoparticles as an approach to rapidly ablate AMLs. Collectively, our experimental approaches represent an innovative and scalable tissue-bioengineering strategy for modeling rare kidney disease in vivo.

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Sigma-Aldrich
CHIR99021, ≥98% (HPLC)
Sigma-Aldrich
Anticuerpo anti-actina, αmúsculo liso- Cy3 monoclonal de ratón, clone 1A4, purified from hybridoma cell culture
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Anti-actina, α-músculo liso monoclonal, clone 1A4, purified from hybridoma cell culture
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Interleukin-1β human, IL-1β, recombinant, expressed in HEK 293 cells, HumanKine®, suitable for cell culture, endotoxin tested