Kidney organoids recapitulate human basement membrane assembly in health and disease
Mychel Morais, Pinyuan Tian, Craig Lawless, Syed Murtuza Baker, Louise Hopkinson, Steven Paul Woods, Mironov Aa, David A. Long, Daniel P. Gale, Telma M.T. Zorn, Susan J. Kimber, Roy Zent, Rachel Lennon
Abstract
Basement membranes (BMs) are complex macromolecular networks underlying all continuous layers of cells. Essential components include collagen IV and laminins, which are affected by human genetic variants leading to a range of debilitating conditions including kidney, muscle, and cerebrovascular phenotypes. We investigated the dynamics of BM assembly in human pluripotent stem cell-derived kidney organoids. We resolved their global BM composition and discovered a conserved temporal sequence in BM assembly that paralleled mammalian fetal kidneys. We identified the emergence of key BM isoforms, which were altered by a pathogenic variant in COL4A5. Integrating organoid, fetal and adult kidney proteomes we found dynamic regulation of BM composition through development to adulthood, and with single-cell transcriptomic analysis we mapped the cellular origins of BM components. Overall, we define the complex and dynamic nature of kidney BM assembly and provide a platform for understanding its wider relevance in human development and disease.