Elizabeth K. Neumann, Nathan Heath Patterson, Leonoor E.M. Tideman, Lukasz G. Migas, Madeline E. Colley, Melissa A. Farrow, Jamie L. Allen, Emilio S. Rivera, Carrie E. Romer, Haichun Yang, Maya Brewer, Kavya Sharman, Raymond C. Harris, Agnes B. Fogo, Danielle B. Gutierrez, Mark P. de Caestecker, Richard M. Caprioli, Raf Van de Plas, and Jeffrey M. Spraggins
SummaryThe human kidney is composed of over 26 cell types that actively coordinate with each other to form higher-order structures, such as the nephron. It is not yet understood how these structures vary throughout a single organ or amongst the same organs within the human population. We have developed an extensive lipid and cellular atlas of the human kidney consisting of over 3 million cells comprising 75,000 functional tissue units (i.e., glomeruli, proximal tubules, distal tubules, and collecting ducts) from 13 human subjects. This atlas was developed using spatially registered and integrated technologies consisting of imaging mass spectrometry, multiplexed immunofluorescence, stained microscopy, and autofluorescence microscopy, to comprehensively probe large (i.e., centimeter-sized) areas of tissue. The cellular organization and lipid profiles of glomeruli, proximal tubules, distal tubules, and collecting ducts were discovered through these multimodal imaging data as well as their intra- and inter-subject variance. Relating the lipid profiles obtained from imaging mass spectrometry to distinct cell types obtained from immunofluorescence allowed us to hypothesize the functional role of specific phospholipids that have not previously been described. These hypotheses include subject characteristics, such as BMI and sex. The integrated data from the aforementioned datasets provide a valuable reference for kidney researchers, are publicly available through the NIH Human Biomolecular Atlas Program (https://portal.hubmapconsortium.org/), and discussed below.