Literature DB >> 25620405

From pathobiology to the targeting of pericytes for the treatment of diabetic retinopathy.

Joseph F Arboleda-Velasquez1, Cammi N Valdez, Christina K Marko, Patricia A D'Amore.   

Abstract

Pericytes, the mural cells that constitute the capillaries along with endothelial cells, have been associated with the pathobiology of diabetic retinopathy; however, therapeutic implications of this association remain largely unexplored. Pericytes appear to be highly susceptible to the metabolic challenges associated with a diabetic environment, and there is substantial evidence that their loss may contribute to microvascular instability leading to the formation of microaneurysms, microhemorrhages, acellular capillaries, and capillary nonperfusion. Since pericytes are strategically located at the interface between the vascular and neural components of the retina, they offer extraordinary opportunities for therapeutic interventions in diabetic retinopathy. Moreover, the availability of novel imaging methodologies now allows for the in vivo visualization of pericytes, enabling a new generation of clinical trials that use pericyte tracking as clinical endpoints. The recognition of multiple signaling mechanisms involved in pericyte development and survival should allow for a renewed interest in pericytes as a therapeutic target for diabetic retinopathy.

Entities:  

Mesh:

Year:  2015        PMID: 25620405      PMCID: PMC5599150          DOI: 10.1007/s11892-014-0573-2

Source DB:  PubMed          Journal:  Curr Diab Rep        ISSN: 1534-4827            Impact factor:   4.810


  122 in total

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4.  Recruitment of pericytes and astrocytes is closely related to the formation of tight junction in developing retinal vessels.

Authors:  Jeong Hun Kim; Jin Hyoung Kim; Young Suk Yu; Dong Hun Kim; Kyu-Won Kim
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Authors:  Maria Enge; Mattias Bjarnegård; Holger Gerhardt; Erika Gustafsson; Mattias Kalén; Noomi Asker; Hans-Peter Hammes; Moshe Shani; Reinhardt Fässler; Christer Betsholtz
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6.  Novel procedures for isolating intact retinal vascular beds from diabetic humans and animal models.

Authors:  N M Laver; W G Robison; B A Pfeffer
Journal:  Invest Ophthalmol Vis Sci       Date:  1993-05       Impact factor: 4.799

Review 7.  Proliferative retinopathies: angiogenesis that blinds.

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Journal:  Int J Biochem Cell Biol       Date:  2009-10-15       Impact factor: 5.085

8.  The angiopoietin/Tie-2 system regulates pericyte survival and recruitment in diabetic retinopathy.

Authors:  Jun Cai; Oksana Kehoe; Gill M Smith; Philip Hykin; Michael E Boulton
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-05       Impact factor: 4.799

9.  Regulation of fibronectin and laminin synthesis by retinal capillary endothelial cells and pericytes in vitro.

Authors:  L J Mandarino; N Sundarraj; J Finlayson; H R Hassell
Journal:  Exp Eye Res       Date:  1993-11       Impact factor: 3.467

10.  Rationale for combination therapy in age-related macular degeneration.

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Review 4.  Blood Brain Barrier Injury in Diabetes: Unrecognized Effects on Brain and Cognition.

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Journal:  J Neuroimmune Pharmacol       Date:  2017-05-29       Impact factor: 4.147

Review 5.  The Protective Effects of Neurotrophins and MicroRNA in Diabetic Retinopathy, Nephropathy and Heart Failure via Regulating Endothelial Function.

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6.  Evaluation of Notch3 Deficiency in Diabetes-Induced Pericyte Loss in the Retina.

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Journal:  J Vasc Res       Date:  2018-10-22       Impact factor: 1.934

7.  Dietary Compound Chrysin Inhibits Retinal Neovascularization with Abnormal Capillaries in db/db Mice.

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Review 8.  Neural Vascular Mechanism for the Cerebral Blood Flow Autoregulation after Hemorrhagic Stroke.

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9.  Therapeutic antibody targeting of Notch3 signaling prevents mural cell loss in CADASIL.

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10.  Ocular TGF-β, Matrix Metalloproteinases, and TIMP-1 Increase with the Development and Progression of Diabetic Retinopathy in Type 2 Diabetes Mellitus.

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