Nerve growth factor enhances clara cell proliferation after lung injury.

Standard

Nerve growth factor enhances clara cell proliferation after lung injury. / Sonar, S S; Schwinge, Dorothee; Kilic, A; Yildirim, A Ö; Conrad, M L; Seidler, K; Müller, B; Renz, H; Nockher, W A.

In: EUR RESPIR J, Vol. 36, No. 1, 1, 2010, p. 105-115.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Sonar, SS, Schwinge, D, Kilic, A, Yildirim, AÖ, Conrad, ML, Seidler, K, Müller, B, Renz, H & Nockher, WA 2010, 'Nerve growth factor enhances clara cell proliferation after lung injury.', EUR RESPIR J, vol. 36, no. 1, 1, pp. 105-115. <http://www.ncbi.nlm.nih.gov/pubmed/20075049?dopt=Citation>

APA

Sonar, S. S., Schwinge, D., Kilic, A., Yildirim, A. Ö., Conrad, M. L., Seidler, K., Müller, B., Renz, H., & Nockher, W. A. (2010). Nerve growth factor enhances clara cell proliferation after lung injury. EUR RESPIR J, 36(1), 105-115. [1]. http://www.ncbi.nlm.nih.gov/pubmed/20075049?dopt=Citation

Vancouver

Sonar SS, Schwinge D, Kilic A, Yildirim AÖ, Conrad ML, Seidler K et al. Nerve growth factor enhances clara cell proliferation after lung injury. EUR RESPIR J. 2010;36(1):105-115. 1.

Bibtex

@article{dd266ddef1d043b6bd351cce19420e28,
title = "Nerve growth factor enhances clara cell proliferation after lung injury.",
abstract = "The lung epithelia facilitate wound closure by secretion of various cytokines and growth factors. Nerve growth factor (NGF) has been well described in airway inflammation; however its likely role in lung repair has not been examined thus far.To investigate the repair function of NGF, experiments were performed in vitro using cultured alveolar epithelial cells and in vivo using naphthalene induced model of Clara epithelial cell injury.Both in vitro and in vivo experiments revealed airway epithelial cell proliferation following injury to be dependent on NGF and the expression of its receptor, tropomyosin-receptor-kinase A. Additionally, NGF also augmented in vitro migration of alveolar type II cells. In vivo, transgenic mice over-expressing NGF in Clara cells (NGFtg) did not reveal any proliferation or alteration in Clara cell phenotype. However, following Clara cell specific injury, proliferation was increased in NGFtg and impaired upon inhibition of NGF. Furthermore, NGF also promoted the expression of collagen I and fibronectin in vitro and in vivo during repair, where significantly higher levels were measured in re-epithelializing NGFtg mice.Our study demonstrates that NGF promotes the proliferation of lung epithelium in vitro and the renewal of Clara cells following lung injury in vivo.",
author = "Sonar, {S S} and Dorothee Schwinge and A Kilic and Yildirim, {A {\"O}} and Conrad, {M L} and K Seidler and B M{\"u}ller and H Renz and Nockher, {W A}",
year = "2010",
language = "Deutsch",
volume = "36",
pages = "105--115",
journal = "EUR RESPIR J",
issn = "0903-1936",
publisher = "European Respiratory Society",
number = "1",

}

RIS

TY - JOUR

T1 - Nerve growth factor enhances clara cell proliferation after lung injury.

AU - Sonar, S S

AU - Schwinge, Dorothee

AU - Kilic, A

AU - Yildirim, A Ö

AU - Conrad, M L

AU - Seidler, K

AU - Müller, B

AU - Renz, H

AU - Nockher, W A

PY - 2010

Y1 - 2010

N2 - The lung epithelia facilitate wound closure by secretion of various cytokines and growth factors. Nerve growth factor (NGF) has been well described in airway inflammation; however its likely role in lung repair has not been examined thus far.To investigate the repair function of NGF, experiments were performed in vitro using cultured alveolar epithelial cells and in vivo using naphthalene induced model of Clara epithelial cell injury.Both in vitro and in vivo experiments revealed airway epithelial cell proliferation following injury to be dependent on NGF and the expression of its receptor, tropomyosin-receptor-kinase A. Additionally, NGF also augmented in vitro migration of alveolar type II cells. In vivo, transgenic mice over-expressing NGF in Clara cells (NGFtg) did not reveal any proliferation or alteration in Clara cell phenotype. However, following Clara cell specific injury, proliferation was increased in NGFtg and impaired upon inhibition of NGF. Furthermore, NGF also promoted the expression of collagen I and fibronectin in vitro and in vivo during repair, where significantly higher levels were measured in re-epithelializing NGFtg mice.Our study demonstrates that NGF promotes the proliferation of lung epithelium in vitro and the renewal of Clara cells following lung injury in vivo.

AB - The lung epithelia facilitate wound closure by secretion of various cytokines and growth factors. Nerve growth factor (NGF) has been well described in airway inflammation; however its likely role in lung repair has not been examined thus far.To investigate the repair function of NGF, experiments were performed in vitro using cultured alveolar epithelial cells and in vivo using naphthalene induced model of Clara epithelial cell injury.Both in vitro and in vivo experiments revealed airway epithelial cell proliferation following injury to be dependent on NGF and the expression of its receptor, tropomyosin-receptor-kinase A. Additionally, NGF also augmented in vitro migration of alveolar type II cells. In vivo, transgenic mice over-expressing NGF in Clara cells (NGFtg) did not reveal any proliferation or alteration in Clara cell phenotype. However, following Clara cell specific injury, proliferation was increased in NGFtg and impaired upon inhibition of NGF. Furthermore, NGF also promoted the expression of collagen I and fibronectin in vitro and in vivo during repair, where significantly higher levels were measured in re-epithelializing NGFtg mice.Our study demonstrates that NGF promotes the proliferation of lung epithelium in vitro and the renewal of Clara cells following lung injury in vivo.

M3 - SCORING: Zeitschriftenaufsatz

VL - 36

SP - 105

EP - 115

JO - EUR RESPIR J

JF - EUR RESPIR J

SN - 0903-1936

IS - 1

M1 - 1

ER -