Stefano Da Sacco

Assistant Professor Of Research Urology

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Overview

~~ About the Lab: Advancing Kidney Regeneration Through Science and Innovation ~~

Dr. Stefano Da Sacco is a research scientist, innovator, and educator at the forefront of kidney regenerative medicine. As an Assistant Professor of Research Urology at the Keck School of Medicine of USC and an investigator at The Saban Research Institute of Children’s Hospital Los Angeles, he leads a multidisciplinary team focused on unraveling the biology of the glomerulus—the kidney’s essential filtration unit—and creating bioengineered solutions for chronic kidney disease (CKD).

With a PhD from the University of Padua and USC, and advanced postdoctoral training in stem cell biology and pediatric urology, Dr. Da Sacco brings a global perspective and deep expertise to his work. His lab integrates stem cell science, organ-on-chip technologies, and disease modeling to push the boundaries of what’s possible in kidney research.

~~ Research Vision ~~

At the heart of Dr. Da Sacco’s research is a fundamental question: How can we protect and repair the kidney’s filtration barrier to better understand, treat, and ultimately prevent kidney disease?

To answer this, his team develops advanced human-relevant platforms that simulate the structure and function of kidney tissue at the cellular and molecular level. These models serve as living testbeds for exploring disease mechanisms, discovering novel biomarkers, and testing potential therapies.

His lab is internationally recognized for its “glomerulus-on-a-chip” platform, a microphysiological system that mimics the specialized architecture and barrier properties of the glomerulus. This innovation allows researchers to observe real-time podocyte behavior, protein leakage, and drug response in a dynamic, patient-relevant context, transforming how we study glomerular diseases such as:
– Membranous Nephropathy
– Alport Syndrome
– Focal Segmental Glomerulosclerosis (FSGS)

~~ Wilms Tumor and Cancer Stem Cell Research ~~

Dr. Da Sacco’s lab is actively investigating the cellular origins and progression of Wilms tumor, the most common pediatric kidney cancer. His team was among the first to identify and characterize cancer stem-like cells within Wilms tumors, uncovering a rare subpopulation with enhanced self-renewal, tumorigenic potential, and resistance to conventional therapies. By using patient-derived samples and advanced molecular profiling, the lab has delineated key surface markers and transcriptional signatures that distinguish these cells from the tumor bulk. This research provides critical insights into tumor hierarchy and relapse mechanisms, and it paves the way for developing targeted therapies that eliminate cancer stem cells, potentially improving outcomes for children with high-risk or recurrent disease.

~~ Scientific Contributions and Impact ~~

Dr. Da Sacco’s lab was among the first to demonstrate how primary renal progenitors and cells can be harnessed to create functional in vitro kidney models. His work has significantly contributed to our understanding of podocyte injury signaling, including the roles of C3a/C3aR signaling pathways.
Beyond modeling disease, his team has been actively collaborating with numerous laboratories worldwide to explore regenerative and reparative therapies, including mitochondrial transplantation, engineered extracellular vesicles, and biocompatible scaffolds for cell delivery.

~~ Funding ~~

Dr. Da Sacco has received research awards from NIH, ASF, and CIRM and is currently supported by NIH/NIDDK RO1s, a PNRC grant award, and Industry collaborations.

Dr. Da Sacco is a member of several professional societies, including the American Society of Nephrology, the International Society of Glomerular Diseases, The Pediatric Nephrology Research Consortium, and ISSNAF. He serves as a reviewer for NIH study sections and the Italian Ministry of Health, among others. He has published extensively in leading scientific journals and is a reviewer for several peer-reviewed publications.

Education and Training

  • University Of Padova, Italy — MS — 2006 — Pharmaceutical Chemistry
  • University Of Padova/USC, Italy/USC — PhD — 2009 — Tissue Engineering and Regenerative Medicine

Research Funding

  • Role of CD93 in podocytopathies.
    NEPHCURE/PNRC Grant Award · Jan 1, 2025 – Dec 31, 2025 · Role: Co-PI
  • Mechanisms involved in podocyte damage in Alport Syndrome
    NIH · R01DK133459 · Aug 15, 2022 – May 31, 2027 · Role: Principal Investigator
  • Novel mechanisms of glomerular injury in primary membranous nephropathy
    NIH · R01DK123234 · Jul 1, 2020 – Jun 30, 2025 · Role: Principal Investigator

Research Keywords

  • Glomerulus-on-a-Chip
  • Glomerular Filtration Barrier
  • Membranous Nephropathy
  • Alport Syndrome
  • Kidney Progenitors
  • Human Kidney Development
  • Amniotic fluid Stem Cells
  • Wilms Tumor

Publications

  • Extracellular vesicle miR-93-5p cargo regulates glomerular endothelial cell damage in Alport syndrome. JCI Insight. 2026 Mar 23; 11(6).. View in PubMed
  • Endothelial cell-released CD93 contributes to podocyte injury in idiopathic nephrotic syndrome. Sci Transl Med. 2026 Jan 14; 18(832):eadw2206.. View in PubMed
  • Response to the Letter to the Editor Entitled “Revisiting Vincristine for FSGS: Proof-of-Mechanism Arrives, but Whom Should we Treat?” Kidney Int Rep. 2026 Mar; 11(3):103748. Mason WJ, Chandler JC, Ga . View in PubMed
  • Editorial: Stem cells and kidney regeneration: transforming renal medicine. Front Bioeng Biotechnol. 2025; 13:1749288.. View in PubMed
  • Vincristine Treatment Protects Against Podocyte Damage in Focal Segmental Glomerulosclerosis. Kidney Int Rep. 2025 Nov; 10(11):3998-4011.. View in PubMed
  • A kidney-specific fasting-mimicking diet induces podocyte reprogramming and restores renal function in glomerulopathy. Sci Transl Med. 2024 10 30; 16(771):eadl5514.. View in PubMed
  • The spatially resolved transcriptome signatures of glomeruli in chronic kidney disease. JCI Insight. 2024 03 22; 9(6).. View in PubMed
  • C3aR-initiated signaling is a critical mechanism of podocyte injury in membranous nephropathy. JCI Insight. 2024 01 16; 9(4).. View in PubMed
  • Mitochondria Transplantation Mitigates Damage in an In Vitro Model of Renal Tubular Injury and in an Ex Vivo Model of DCD Renal Transplantation. Ann Surg. 2023 12 01; 278(6):e1313-e1326.. View in PubMed
  • Identification and Characterization of the Wilms Tumor Cancer Stem Cell. Adv Sci (Weinh). 2023 07; 10(20):e2206787.. View in PubMed