Retinal proteome associated with bradykinin-induced edema.


Journal

Experimental eye research
ISSN: 1096-0007
Titre abrégé: Exp Eye Res
Pays: England
ID NLM: 0370707

Informations de publication

Date de publication:
09 2019
Historique:
received: 03 12 2018
revised: 19 06 2019
accepted: 22 07 2019
pubmed: 28 7 2019
medline: 15 2 2020
entrez: 28 7 2019
Statut: ppublish

Résumé

The plasma kallikrein-stimulated generation of bradykinin (BK) has been implicated in diabetic macular edema (DME). This study characterizes the effects of BK on the ultrastructure and proteome of the rat retina. The effects of intravitreal injection of BK on retinal thickness and vascular ultrastructure in Sprague Dawley rats were analyzed and compared with the effects of VEGF using spectral-domain optical coherence tomography. At 24 h post intravitreal injection of BK or saline vehicle retina were harvested and solubilized proteins were analyzed by mass spectrometry-based proteomics. Proteins were identified using X!Tandem and spectral counts were used as a semiquantitative measurement of protein abundance. Proteins identified from retinal extracts were annotated by Gene Ontology (GO) slim terms and compared with a human DME vitreous proteome. Intravitreal injection of BK and VEGF induced transient increases in retinal thickness of 46 μm (24.6%, p = 0.015) and 39 μm (20.3%, p = 0.004), respectively at 24 h, which were resolved to baseline thicknesses at 96 h post injection. BK and VEGF also increased retinal vessel diameters and tortuosity at 24 h post intravitreal injection. Proteomic analyses identified 1757 non-redundant proteins in the rat retina, including 1739 and 1725 proteins from BK- and saline control-injected eyes, respectively. Eighteen proteins, including two proteins associated with intercellular junctions, filamin A and actinin alpha 4, were decreased by at least 50% (p < 0.05) in retina from BK-injected eyes compare with retina from eyes injected with saline. In addition, 32 proteins were increased by > 2-fold (p < 0.05) in retina from BK-injected eyes. Eight proteins, including complement C3, were identified to be increased in both BK-stimulated rat retina and in human DME vitreous. Western blot analysis showed that Complement 3 levels in vitreous from BK-injected eyes in rats and clinical DME samples were increased by 6.6-fold (p = 0.039) and 4.3-fold (p = 0.02), compared with their respective controls. In summary, this study identifies protein changes in rat retina that are associated with BK-induced retinal thickening, including 8 proteins that were previously reported to be increased in the human DME vitreous proteome.

Identifiants

pubmed: 31351056
pii: S0014-4835(18)30880-7
doi: 10.1016/j.exer.2019.107744
pii:
doi:

Substances chimiques

Proteome 0
Vascular Endothelial Growth Factor A 0
Vasodilator Agents 0
Plasma Kallikrein EC 3.4.21.34
Bradykinin S8TIM42R2W

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

107744

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Nivetha Murugesan (N)

Joslin Diabetes Center, Boston, MA, USA; KalVista Pharmaceuticals Inc, Cambridge, MA, USA.

Ward Fickweiler (W)

Joslin Diabetes Center, Boston, MA, USA; Beetham Eye Institute. Joslin Diabetes Center, Boston, MA, USA.

Allen C Clermont (AC)

Joslin Diabetes Center, Boston, MA, USA; Beetham Eye Institute. Joslin Diabetes Center, Boston, MA, USA.

Qunfang Zhou (Q)

Chinese Academy of Sciences, Beijing, China.

Edward P Feener (EP)

Joslin Diabetes Center, Boston, MA, USA; KalVista Pharmaceuticals Inc, Cambridge, MA, USA. Electronic address: epf@kalvista.com.

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Classifications MeSH