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Purpose: To investigate the incidence and clinical implications of intracellular dark endothelial spots (IDES) following penetrating keratoplasty (PK) and their association with endothelial cell density (ECD) loss and graft failure.
Design: Retrospective clinical cohort study.
Methods: This study included 71 eyes that underwent PK and 33 control eyes that underwent cataract surgery. We evaluated the presence of IDES on specular microscopy, ECD, preoperative aqueous humor (AqH) protein and cytokine levels using Luminex. Follow-up examinations were conducted for 36 months postoperatively. Logistic regression analysis was performed to identify clinical risk factors for IDES development and graft survival.
Results: IDES developed in 40 PK eyes (56.3%). IDES was associated with exhibiting significantly lower ECD at all postoperative stages (P < .001) and higher secondary graft failure rates compared to IDES-negative eyes (P = .014). Risk factors for IDES development after PK included the presence of an intraocular lens (P = .028), multiple previous intraocular surgeries (P = .0076), and lower preoperative donor ECD (P = .004). IDES-positive eyes with an ECD decrease of more than 50% within 12 months postoperatively had significantly higher preoperative AqH protein levels compared to those without such a decrease (P = .031). Kaplan-Meier analysis showed a higher rate of graft failure in IDES-positive eyes compared to those without (P = .014).
Conclusions: The development of IDES after PK appears to be associated with higher ECD loss and graft failure, suggesting its potential as a biomarker for endothelial cell loss and graft prognosis.
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http://dx.doi.org/10.1016/j.ajo.2025.08.022 | DOI Listing |
J Biomed Sci
September 2025
Division of Gastroenterology, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, MA, USA.
Oncometabolites are aberrant metabolic byproducts that arise from mutations in enzymes of the tricarboxylic acid (TCA) cycle or related metabolic pathways and play central roles in tumor progression and immune evasion. Among these, 2-hydroxyglutarate (2-HG), succinate, and fumarate are the most well-characterized, acting as competitive inhibitors of α-ketoglutarate-dependent dioxygenases to alter DNA and histone methylation, cellular differentiation, and hypoxia signaling. More recently, itaconate, an immunometabolite predominantly produced by activated macrophages, has been recognized for its dual roles in modulating inflammation and tumor immunity.
View Article and Find Full Text PDFStem Cell Rev Rep
September 2025
Paris Cité University, INSERM UMR-S 970, Paris Cardiovascular Research Centre, Paris, France.
Endothelial Colony-Forming Cells (ECFCs) are recognized as key vasculogenic progenitors in humans and serve as valuable liquid biopsies for diagnosing and studying vascular disorders. In a groundbreaking study, Anceschi et al. present a novel, integrative strategy that combines ECFCs loaded with gold nanorods (AuNRs) to enhance tumor radiosensitization through localized hyperthermia.
View Article and Find Full Text PDFMol Syst Biol
September 2025
Department of Medicine, Division of Cardiovascular Medicine, Stanford University, Stanford, CA, USA.
Vascular sites have distinct susceptibility to atherosclerosis and aneurysm, yet the epigenomic and transcriptomic underpinning of vascular site-specific disease risk is largely unknown. Here, we performed single-cell chromatin accessibility (scATACseq) and gene expression profiling (scRNAseq) of mouse vascular tissue from three vascular sites. Through interrogation of epigenomic enhancers and gene regulatory networks, we discovered key regulatory enhancers to not only be cell type, but vascular site-specific.
View Article and Find Full Text PDFCell Mol Immunol
September 2025
Pediatric Intensive Care Unit, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences); Department of Immunology, School of Basic Medical Sciences; Department of Clinical Laboratory, the Third Affiliated Hospital of Southern Medical University, Southern Medical University, Gua
Communication between group 3 innate lymphoid cells (ILC3) and other immune cells, as well as intestinal epithelial cells, is pivotal in regulating intestinal inflammation. This study, for the first time, underscores the importance of crosstalk between intestinal endothelial cells (ECs) and ILC3. Our single-cell transcriptome analysis combined with protein expression detection revealed that ECs significantly increased the population of interleukin (IL)-22 ILC3 through interactions mediated by endothelin-1 (ET-1) and its receptor endothelin A receptor (EDNRA).
View Article and Find Full Text PDFLeukemia
September 2025
University Children's Hospital Zurich, Pediatric Oncology and Children's Research Center, Zurich, Switzerland.
Acute lymphoblastic leukemia (ALL) preferentially localizes in the bone marrow (BM) and displays recurrent patterns of medullary and extra-medullary involvement. Leukemic cells exploit their niche for propagation and survive selective pressure by chemotherapy in the BM microenvironment, suggesting the existence of protective mechanisms. Here, we established a three-dimensional (3D) BM mimic with human mesenchymal stromal cells and endothelial cells that resemble vasculature-like structures to explore the interdependence of leukemic cells with their microenvironment.
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