bioRxivGenomicsPreprint
An Integrated muti-omics cell atlas of the human trabecular meshwork and ciliary body
Jinjing JianiD, Xuan BaoiD, Jun WangiD, Y ZhengiD, Jin LiiD, Jianming ShaoiD, Tingting YangiD, Ismail Yaman, Jean LiiD, Han CheniD, Nicholas G. TolmaniD, Richard H. ScheuermanniD, Jie ZhengiD, Carl SheridaniD, Yutao LiuiD, Yiqin DuiD, Revathi BalasubramanianiD, Gulab S ZodeiD, Simon W. M. JohniD, J. Timothy Stout, Dan Stamer, Yumei Li, Rui CheniD
Abstract
The trabecular meshwork (TM) and ciliary body (CB) regulate aqueous humor dynamics and intraocular pressure (IOP), and TM/Schlemms canal (SC) dysfunction underlies glaucoma. Here, we present a spatially resolved multi-omics atlas of human TM and CB, integrating snRNA-seq, scRNA-seq, and snATAC-seq from over one million cells and nuclei across 112 donors with Xenium spatial transcriptomics. We identified 9 major cell classes and 21 cell types, revealing heterogeneity, including undercharacterized fibroblast and epithelial subpopulations. Spatial mapping supported TM fibroblast zonation and CB epithelial organization. Regulatory analyses identified cell type-specific programs, including OTX/PAX networks in CB epithelium and SMAD3/TGF-{beta} signaling in fibroblasts. Integration with glaucoma loci showed enrichment of non-coding variants in regulatory elements associated with POAG and PACG. Age- and ancestry-associated remodeling revealed divergent fibroblast aging with increased PIEZO1, suggesting impaired outflow and elevated IOP. Together, this high-resolution atlas links cellular, regulatory, and genetic variation to anterior segment function and glaucoma susceptibility.
- organism: human
- assay: snRNA-seq
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: gene regulatory network inference
- research focus: GWAS / association mapping
- approach: statistical model
- approach: experimental assay
- Citations
- 0
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