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  1. Article ; Online: Advanced Glycation End Products Upregulate CD40 in Human Retinal Endothelial and Müller Cells: Relevance to Diabetic Retinopathy.

    Portillo, Jose-Andres C / Pfaff, Amelia / Vos, Sarah / Weng, Matthew / Nagaraj, Ram H / Subauste, Carlos S

    Cells

    2024  Volume 13, Issue 5

    Abstract: CD40 induces pro-inflammatory responses in endothelial and Müller cells and is required for the development of diabetic retinopathy (DR). CD40 is upregulated in these cells in patients with DR. CD40 upregulation is a central feature of CD40-driven ... ...

    Abstract CD40 induces pro-inflammatory responses in endothelial and Müller cells and is required for the development of diabetic retinopathy (DR). CD40 is upregulated in these cells in patients with DR. CD40 upregulation is a central feature of CD40-driven inflammatory disorders. What drives CD40 upregulation in the diabetic retina remains unknown. We examined the role of advanced glycation end products (AGEs) in CD40 upregulation in endothelial cells and Müller cells. Human endothelial cells and Müller cells were incubated with unmodified or methylglyoxal (MGO)-modified fibronectin. CD40 expression was assessed by flow cytometry. The expression of ICAM-1 and CCL2 was examined by flow cytometry or ELISA after stimulation with CD154 (CD40 ligand). The expression of carboxymethyl lysine (CML), fibronectin, and laminin as well as CD40 in endothelial and Müller cells from patients with DR was examined by confocal microscopy. Fibronectin modified by MGO upregulated CD40 in endothelial and Müller cells. CD40 upregulation was functionally relevant. MGO-modified fibronectin enhanced CD154-driven upregulation of ICAM-1 and CCL2 in endothelial and Müller cells. Increased CD40 expression in endothelial and Müller cells from patients with DR was associated with increased CML expression in fibronectin and laminin. These findings identify AGEs as inducers of CD40 upregulation in endothelial and Müller cells and enhancers of CD40-dependent pro-inflammatory responses. CD40 upregulation in these cells is associated with higher CML expression in fibronectin and laminin in patients with DR. This study revealed that CD40 and AGEs, two important drivers of DR, are interconnected.
    MeSH term(s) Humans ; Diabetic Retinopathy/metabolism ; Intercellular Adhesion Molecule-1/metabolism ; Fibronectins/metabolism ; Ependymoglial Cells/metabolism ; Endothelial Cells/metabolism ; Magnesium Oxide/metabolism ; Retina/metabolism ; CD40 Antigens/metabolism ; CD40 Ligand/metabolism ; Laminin/metabolism ; Glycation End Products, Advanced/metabolism ; Diabetes Mellitus/metabolism
    Chemical Substances Intercellular Adhesion Molecule-1 (126547-89-5) ; Fibronectins ; Magnesium Oxide (3A3U0GI71G) ; CD40 Antigens ; CD40 Ligand (147205-72-9) ; Laminin ; Glycation End Products, Advanced
    Language English
    Publishing date 2024-02-29
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2661518-6
    ISSN 2073-4409 ; 2073-4409
    ISSN (online) 2073-4409
    ISSN 2073-4409
    DOI 10.3390/cells13050429
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: CD40 Upregulation in the Retina of Patients With Diabetic Retinopathy: Association With TRAF2/TRAF6 Upregulation and Inflammatory Molecule Expression.

    Vos, Sarah / Aaron, Rachel / Weng, Matthew / Daw, Jad / Rodriguez-Rivera, Emmanuel / Subauste, Carlos S

    Investigative ophthalmology & visual science

    2023  Volume 64, Issue 7, Page(s) 17

    Abstract: Purpose: CD40 is upregulated in the retinas of diabetic mice, drives pro-inflammatory molecule expression, and promotes diabetic retinopathy. The role of CD40 in diabetic retinopathy in humans is unknown. Upregulation of CD40 and its downstream ... ...

    Abstract Purpose: CD40 is upregulated in the retinas of diabetic mice, drives pro-inflammatory molecule expression, and promotes diabetic retinopathy. The role of CD40 in diabetic retinopathy in humans is unknown. Upregulation of CD40 and its downstream signaling molecules TNF receptor associated factors (TRAFs) is a key feature of CD40-driven inflammatory disorders. We examined the expression of CD40, TRAF2, and TRAF6 as well as pro-inflammatory molecules in retinas from patients with diabetic retinopathy.
    Methods: Posterior poles from patients with diabetic retinopathy and non-diabetic controls were stained with antibodies against von Willebrand factor (labels endothelial cells), cellular retinaldehyde-binding protein (CRALBP), or vimentin (both label Müller cells) plus antibodies against CD40, TRAF2, TRAF6, ICAM-1, CCL2, TNF-α, and/or phospho-Tyr783 phospholipase Cγ1 (PLCγ1). Sections were analyzed by confocal microscopy.
    Results: CD40 expression was increased in endothelial and Müller cells from patients with diabetic retinopathy. CD40 was co-expressed with ICAM-1 in endothelial cells and with CCL2 in Müller cells. TNF-α was detected in retinal cells from these patients, but these cells lacked endothelial/Müller cell markers. CD40 in Müller cells from patients with diabetic retinopathy co-expressed activated phospholipase Cγ1, a molecule that induces TNF-α expression in myeloid cells in mice. CD40 upregulation in endothelial cells and Müller cells from patients with diabetic retinopathy was accompanied by TRAF2 and TRAF6 upregulation.
    Conclusions: CD40, TRAF2, and TRAF6 are upregulated in patients with diabetic retinopathy. CD40 associates with expression of pro-inflammatory molecules. These findings suggest that CD40-TRAF signaling may promote pro-inflammatory responses in the retinas of patients with diabetic retinopathy.
    MeSH term(s) Humans ; Mice ; Animals ; TNF Receptor-Associated Factor 2/genetics ; TNF Receptor-Associated Factor 2/metabolism ; Diabetic Retinopathy/metabolism ; TNF Receptor-Associated Factor 6/metabolism ; Intercellular Adhesion Molecule-1/metabolism ; Up-Regulation ; Endothelial Cells/metabolism ; Tumor Necrosis Factor-alpha/metabolism ; Diabetes Mellitus, Experimental/metabolism ; CD40 Antigens/genetics ; Retina/metabolism ; Phospholipases/metabolism
    Chemical Substances TNF Receptor-Associated Factor 2 ; TNF Receptor-Associated Factor 6 ; Intercellular Adhesion Molecule-1 (126547-89-5) ; Tumor Necrosis Factor-alpha ; CD40 Antigens ; Phospholipases (EC 3.1.-)
    Language English
    Publishing date 2023-04-25
    Publishing country United States
    Document type Journal Article
    ZDB-ID 391794-0
    ISSN 1552-5783 ; 0146-0404
    ISSN (online) 1552-5783
    ISSN 0146-0404
    DOI 10.1167/iovs.64.7.17
    Database MEDical Literature Analysis and Retrieval System OnLINE

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