Enhanced podocyte differentiation and changing drug toxicity sensitivity through pressure-controlled mechanical filtration stress on a glomerulus-on-a-chip

• Published in: Lab on a chip Vol. 23; no. 3; pp. 437 - 45
• Main Authors: Doi, Kotaro, Kimura, Hiroshi, Kim, Soo Hyeon, Kaneda, Shohei, Wada, Takehiko, Tanaka, Tetsuhiro, Shimizu, Akira, Sano, Takanori, Chikamori, Masamichi, Shinohara, Marie, Matsunaga, Yukiko T, Nangaku, Masaomi, Fujii, Teruo
• Format: Journal Article
• Language: English
• Published: England Royal Society of Chemistry 31.01.2023
• Subjects: Animals; Drug-Related Side Effects and Adverse Reactions; Filtration; Gene expression; Glomerulus; Hypertension; Kidney diseases; Kidney Diseases - chemically induced; Kidney Diseases - metabolism; Kidney Glomerulus - metabolism; Lab-On-A-Chip Devices; Mice; Pharmacology; Physiological effects; Podocytes - metabolism; Proteinuria; Toxicity
• ISSN: 1473-0197; 1473-0189
• DOI: 10.1039/d2lc00941b

Podocytes, localized in the glomerulus, are a prognostic factor of proteinuria in kidney disease and are exposed to distinct physiological stimuli from basal to apical filtration flow. Research studies on drug discovery and disease modeling for glomerulopathy have developed a glomerulus-on-a-chip and studied podocyte mechanobiology to realize alternative methods to animal experiments. However, the effect of filtration stimulus on podocytes has remained unclear. Herein, we report the successful development of a user-friendly filtration culture device and system that can precisely control the filtration flow using air pressure control by incorporating a commercially available culture insert. It allows mouse podocytes to be cultured under filtration conditions for three days with a guarantee of maintaining the integrity of the podocyte layer. Using our system, this study demonstrated that podocyte damage caused by hyperfiltration resulting from glomerular hypertension, a common pathophysiology of many glomerulopathies, was successfully recapitulated and that filtration stimulus promotes the maturation of podocytes in terms of their morphology and gene expression. Furthermore, we demonstrated that filtration stimulus induced different drug responsiveness in podocytes than those seen under static conditions, and that the difference in drug responsiveness was dependent on the pharmacological mechanism. Overall, this study has revealed differentiating and pharmacodynamic properties of filtration stimulus and brings new insights into the research field of podocyte mechanobiology towards the realization of glomerulus-on-a-chip. The development of a filtration flow device system with precisely controlled pressure revealed the mechanobiology of filtration flow to podocytes regarding morphological and gene expression maturation and increased sensitivity to toxic drugs.