Blocking of Connexin-Mediated Communication Promotes Neuroprotection during Acute Degeneration Induced by Mechanical Trauma


Autoria(s): Paschon, Vera; Higa, Guilherme Shigueto Vilar; Resende, Rodrigo Ribeiro; Britto, Luiz Roberto Giorgetti de; Kihara, Alexandre Hiroaki
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

12/10/2013

12/10/2013

2012

Resumo

Accruing evidence indicates that connexin (Cx) channels in the gap junctions (GJ) are involved in neurodegeneration after injury. However, studies using KO animal models endowed apparently contradictory results in relation to the role of coupling in neuroprotection. We analyzed the role of Cx-mediated communication in a focal lesion induced by mechanical trauma of the retina, a model that allows spatial and temporal definition of the lesion with high reproducibility, permitting visualization of the focus, penumbra and adjacent areas. Cx36 and Cx43 exhibited distinct gene expression and protein levels throughout the neurodegeneration progress. Cx36 was observed close to TUNEL-positive nuclei, revealing the presence of this protein surrounding apoptotic cells. The functional role of cell coupling was assessed employing GJ blockers and openers combined with lactate dehydrogenase (LDH) assay, a direct method for evaluating cell death/viability. Carbenoxolone (CBX), a broad-spectrum GJ blocker, reduced LDH release after 4 hours, whereas quinine, a Cx36-channel specific blocker, decreased LDH release as early as 1 hour after lesion. Furthermore, analysis of dying cell distribution confirmed that the use of GJ blockers reduced apoptosis spread. Accordingly, blockade of GJ communication during neurodegeneration with quinine, but not CBX, caused downregulation of initial and effector caspases. To summarize, we observed specific changes in Cx gene expression and protein distribution during the progress of retinal degeneration, indicating the participation of these elements in acute neurodegeneration processes. More importantly, our results revealed that direct control of GJ channels permeability may take part in reliable neuroprotection strategies aimed to rapid, fast treatment of mechanical trauma in the retina.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Universidade Federal do ABC (UFABC)

Universidade Federal do ABC (UFABC)

Universidade de Sao Paulo (USP)

Universidade de Sao Paulo (USP)

Identificador

PLOS ONE, SAN FRANCISCO, v. 7, n. 9, supl. 4, Part 1-2, pp. 1755-1760, SEP 20, 2012

1932-6203

http://www.producao.usp.br/handle/BDPI/34183

10.1371/journal.pone.0045449

http://dx.doi.org/10.1371/journal.pone.0045449

Idioma(s)

eng

Publicador

PUBLIC LIBRARY SCIENCE

SAN FRANCISCO

Relação

PLOS ONE

Direitos

openAccess

Copyright PUBLIC LIBRARY SCIENCE

Palavras-Chave #NEURONAL GAP-JUNCTIONS #DEVELOPING RETINA #MOUSE RETINA #EXPRESSION #CELLS #NEURODEGENERATION #HISTOGENESIS #APOPTOSIS #MICRORNA #MODELS #MULTIDISCIPLINARY SCIENCES
Tipo

article

original article

publishedVersion