| Literature DB >> 32259357 |
Yi Zhou1,2, Xiaobo Xia2, Enzhi Yang1, Yiwen Wang1,2, Kacey G Marra3,4, C Ross Ethier5, Joel S Schuman6, Yiqin Du1,4,7.
Abstract
The trabecular meshwork (TM) is an ocular tissue that maintains intraocular pressure (IOP) within a physiologic range. Glaucoma patients have reduced TM cellularity and, frequently, elevated IOP. To establish a stem cell-based approach to restoring TM function and normalizing IOP, human adipose-derived stem cells (ADSCs) were induced to differentiate to TM cells in vitro. These ADSC-TM cells displayed a TM cell-like genotypic profile, became phagocytic, and responded to dexamethasone stimulation, characteristic of TM cells. After transplantation into naive mouse eyes, ADSCs and ADSC-TM cells integrated into the TM tissue, expressed TM cell markers, and maintained normal IOP, outflow facility, and extracellular matrix. Cell migration and affinity results indicated that the chemokine pair CXCR4/SDF1 may play an important role in ADSC-TM cell homing. Our study demonstrates the possibility of applying autologous or allogeneic ADSCs and ADSC-TM cells as a potential treatment to restore TM structure and function in glaucoma.Entities:
Keywords: adipose stem cells; differentiation; homing; integration; trabecular meshwork
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Year: 2020 PMID: 32259357 PMCID: PMC7254553 DOI: 10.1096/fj.201902326R
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191