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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Pulmonary Inflammation Is Regulated by the Levels of the Vesicular Acetylcholine Transporter

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Autor(es):
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Pinheiro, Nathalia M. [1] ; Miranda, Claudia J. C. P. [1] ; Perini, Adenir [1] ; Camara, Niels O. S. [2] ; Costa, Soraia K. P. [3] ; Alonso-Vale, Maria Isabel C. [4] ; Caperuto, Luciana C. [4] ; Tiberio, Iolanda F. L. C. [1] ; Prado, Marco Antonio M. [5, 6] ; Martins, Milton A. [1] ; Prado, Vania F. [5, 6] ; Prado, Carla M. [1, 4]
Número total de Autores: 12
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Sch Med, Dept Med, Sao Paulo - Brazil
[2] Univ Sao Paulo, Dept Immunol, Inst Biomed Sci, Sao Paulo - Brazil
[3] Univ Sao Paulo, Dept Pharmacol, Inst Biomed Sci, Sao Paulo - Brazil
[4] Univ Fed Sao Paulo, Dept Biol Sci, Diadema - Brazil
[5] Univ Western Ontario, Dept Anat & Cell Biol, London, ON - Canada
[6] Univ Western Ontario, Dept Physiol & Pharmacol, Robarts Res Inst, Mol Med Grp, London, ON - Canada
Número total de Afiliações: 6
Tipo de documento: Artigo Científico
Fonte: PLoS One; v. 10, n. 3 MAR 27 2015.
Citações Web of Science: 16
Resumo

Acetylcholine (ACh) plays a crucial role in physiological responses of both the central and the peripheral nervous system. Moreover, ACh was described as an anti-inflammatory mediator involved in the suppression of exacerbated innate response and cytokine release in various organs. However, the specific contributions of endogenous release ACh for inflammatory responses in the lung are not well understood. To address this question we have used mice with reduced levels of the vesicular acetylcholine transporter (VAChT), a protein required for ACh storage in secretory vesicles. VAChT deficiency induced airway inflammation with enhanced TNF-alpha and IL-4 content, but not IL-6, IL-13 and IL-10 quantified by ELISA. Mice with decreased levels of VAChT presented increased collagen and elastic fibers deposition in airway walls which was consistent with an increase in inflammatory cells positive to MMP-9 and TIMP-1 in the lung. In vivo lung function evaluation showed airway hyperresponsiveness to methacholine in mutant mice. The expression of nuclear factor-kappa B (p65-NF-kappa B) in lung of VAChT-deficient mice were higher than in wild-type mice, whereas a decreased expression of janus-kinase 2 (JAK2) was observed in the lung of mutant animals. Our findings show the first evidence that cholinergic deficiency impaired lung function and produce local inflammation. Our data supports the notion that cholinergic system modulates airway inflammation by modulation of JAK2 and NF-kappa B pathway. We proposed that intact cholinergic pathway is necessary to maintain the lung homeostasis. (AU)

Processo FAPESP: 08/55359-5 - Avaliação da função e da histopatologia pulmonar em modelo experimental de redução da função colinérgica em camundongos geneticamente modificados
Beneficiário:Carla Máximo Prado
Linha de fomento: Auxílio à Pesquisa - Apoio a Jovens Pesquisadores