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Biology subjects

Eng, D. G.

Publications and source records attributed to Eng, D. G..

2 recordsLinked to original sources

High-throughput, organ-scale 3D tubule tracking using TubuleMAP

Advances in tissue clearing and lightsheet microscopy enable mesoscale imaging of intact and convoluted tubular networks, yet analytical tools to map tubule continuity and assess injury patterns within and across tubules are limited. Here, we introduce TubuleMAP, a semi-automated pipeline for 3D tubule tracking and reconstruction that adapts to various morphological and staining patterns, leverages parallel processing of terabyte-scale data for large-scale analysis of tubular networks, and uses a napari interface for human oversight. Using TubuleMAP, we reconstruct 1,000 intact mouse nephrons in [~]1-millimeter-thick kidney slab with [~]400-fold higher throughput and <1% human effort compared to prior approaches. These reconstructions enable analysis of mesoscale nephron organization, quantitative profiling of pathologic morphologies, whole-nephron cytometry, and identification of rare morphologies at unprecedented scales. We demonstrate generalizability by reconstructing all seminiferous tubules in a mouse testis within a day. TubuleMAP is released as an open-source Python package.

bioengineering↗

A single cell atlas of mouse podocytes upon injury identifies kidney zone-dependent responses.

There are regional differences in the kidney in focal segmental glomerulosclerosis (FSGS) where podocyte injury is more severe in the juxta-medulla (JM) compared to the outer cortex (OC). Single nuclear RNA-sequencing was performed to determine any regional transcriptomic differences. 1055 differentially expressed genes (DEGs) were identified between healthy OC and JM podocytes. Of 53 podocyte canonical genes, only Magi1 and Mapt, and Npnt were higher in healthy OC and JM podocytes respectively. Hallmark pathway analysis showed that in normal mice, healthy JM podocytes are enriched for oxidative phosphorylation, glycolysis and fatty acid metabolism compared to OC podocytes. At day 7 in an experimental FSGS model induced in mice with a cytopathic anti-podocyte antibody, 226 and 225 DEGs were higher in OC and JM podocytes respectively, and 166 overlapped. Five podocyte subclusters were identified, of which the most severe (subcluster 4) was enriched for a senescence phenotype, including the p53 pathway. Inducing FSGS in mice in which p53 was deleted specifically in podocytes had lower glomerular injury compared to diseased wildtype mice. These results are consistent with differences in podocytes in the OC and JM, which might underlie regional differences in FSGS.

bioinformatics↗