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Items: 1 to 20 of 110

1.

Lung fibrosis-associated surfactant protein A1 and C variants induce latent transforming growth factor β1 secretion in lung epithelial cells.

Maitra M, Dey M, Yuan WC, Nathanielsz PW, Garcia CK.

J Biol Chem. 2013 Sep 20;288(38):27159-71. doi: 10.1074/jbc.M113.475335. Epub 2013 Aug 7. Retraction in: J Biol Chem. 2015 Aug 28;290(35):21407.

2.

Mutant surfactant A2 proteins associated with familial pulmonary fibrosis and lung cancer induce TGF-β1 secretion.

Maitra M, Cano CA, Garcia CK.

Proc Natl Acad Sci U S A. 2012 Dec 18;109(51):21064-9. doi: 10.1073/pnas.1217069110. Epub 2012 Dec 5. Retraction in: Proc Natl Acad Sci U S A. 2015 Sep 15;112(37):E5222.

3.

Histone deacetylase inhibitor restores surfactant protein-C expression in alveolar-epithelial type II cells and attenuates bleomycin-induced pulmonary fibrosis in vivo.

Ota C, Yamada M, Fujino N, Motohashi H, Tando Y, Takei Y, Suzuki T, Takahashi T, Kamata S, Makiguchi T, Yamaya M, Kubo H.

Exp Lung Res. 2015;41(8):422-34. doi: 10.3109/01902148.2015.1060275. Epub 2015 Jul 7.

PMID:
26151196
4.

Surfactant protein D attenuates sub-epithelial fibrosis in allergic airways disease through TGF-β.

Ogawa H, Ledford JG, Mukherjee S, Aono Y, Nishioka Y, Lee JJ, Izumi K, Hollingsworth JW.

Respir Res. 2014 Nov 29;15:143. doi: 10.1186/s12931-014-0143-9.

5.

Interactions between β-catenin and transforming growth factor-β signaling pathways mediate epithelial-mesenchymal transition and are dependent on the transcriptional co-activator cAMP-response element-binding protein (CREB)-binding protein (CBP).

Zhou B, Liu Y, Kahn M, Ann DK, Han A, Wang H, Nguyen C, Flodby P, Zhong Q, Krishnaveni MS, Liebler JM, Minoo P, Crandall ED, Borok Z.

J Biol Chem. 2012 Mar 2;287(10):7026-38. doi: 10.1074/jbc.M111.276311. Epub 2012 Jan 12.

6.

The role of transforming growth factors beta1 and beta3 in pre- and post-natal pulmonary surfactant development.

Qiu L, Deng C, Fu Z, Guo C.

Cell Biol Int. 2011 Mar;35(3):287-92. doi: 10.1042/CBI20090486.

PMID:
20973761
7.

MicroRNA-326 regulates profibrotic functions of transforming growth factor-β in pulmonary fibrosis.

Das S, Kumar M, Negi V, Pattnaik B, Prakash YS, Agrawal A, Ghosh B.

Am J Respir Cell Mol Biol. 2014 May;50(5):882-92. doi: 10.1165/rcmb.2013-0195OC.

8.

Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis.

Selman M, Lin HM, Montaño M, Jenkins AL, Estrada A, Lin Z, Wang G, DiAngelo SL, Guo X, Umstead TM, Lang CM, Pardo A, Phelps DS, Floros J.

Hum Genet. 2003 Nov;113(6):542-50. Epub 2003 Sep 6.

PMID:
13680361
9.

High-Mobility Group Box 1 Mediates Epithelial-to-Mesenchymal Transition in Pulmonary Fibrosis Involving Transforming Growth Factor-β1/Smad2/3 Signaling.

Li LC, Li DL, Xu L, Mo XT, Cui WH, Zhao P, Zhou WC, Gao J, Li J.

J Pharmacol Exp Ther. 2015 Sep;354(3):302-9. doi: 10.1124/jpet.114.222372. Epub 2015 Jun 30.

10.

Angiotensin-TGF-beta 1 crosstalk in human idiopathic pulmonary fibrosis: autocrine mechanisms in myofibroblasts and macrophages.

Uhal BD, Kim JK, Li X, Molina-Molina M.

Curr Pharm Des. 2007;13(12):1247-56. Review.

PMID:
17504233
11.

Surfactant protein A binds TGF-β1 with high affinity and stimulates the TGF-β pathway.

Willems CH, Zimmermann LJ, Kloosterboer N, Kramer BW, van Iwaarden JF.

Innate Immun. 2014 Feb;20(2):192-9. doi: 10.1177/1753425913488012. Epub 2013 May 17.

PMID:
23685990
12.

Protective effect of Ac-SDKP on alveolar epithelial cells through inhibition of EMT via TGF-β1/ROCK1 pathway in silicosis in rat.

Deng H, Xu H, Zhang X, Sun Y, Wang R, Brann D, Yang F.

Toxicol Appl Pharmacol. 2016 Mar 1;294:1-10. doi: 10.1016/j.taap.2016.01.010. Epub 2016 Jan 16.

PMID:
26785300
13.

Surfactant protein A2 mutations associated with pulmonary fibrosis lead to protein instability and endoplasmic reticulum stress.

Maitra M, Wang Y, Gerard RD, Mendelson CR, Garcia CK.

J Biol Chem. 2010 Jul 16;285(29):22103-13. doi: 10.1074/jbc.M110.121467. Epub 2010 May 13.

14.

Induction of epithelial-mesenchymal transition in alveolar epithelial cells by transforming growth factor-beta1: potential role in idiopathic pulmonary fibrosis.

Willis BC, Liebler JM, Luby-Phelps K, Nicholson AG, Crandall ED, du Bois RM, Borok Z.

Am J Pathol. 2005 May;166(5):1321-32.

15.

Overexpression of c-Met and CD44v6 receptors contributes to autocrine TGF-β1 signaling in interstitial lung disease.

Ghatak S, Bogatkevich GS, Atnelishvili I, Akter T, Feghali-Bostwick C, Hoffman S, Fresco VM, Fuchs JC, Visconti RP, Markwald RR, Padhye SB, Silver RM, Hascall VC, Misra S.

J Biol Chem. 2014 Mar 14;289(11):7856-72. doi: 10.1074/jbc.M113.505065. Epub 2013 Dec 9.

16.

TGF-beta1 in SP-A preparations influence immune suppressive properties of SP-A on human CD4+ T lymphocytes.

Kunzmann S, Wright JR, Steinhilber W, Kramer BW, Blaser K, Speer CP, Schmidt-Weber C.

Am J Physiol Lung Cell Mol Physiol. 2006 Oct;291(4):L747-56. Epub 2006 Apr 28.

17.

ERK5 inhibition ameliorates pulmonary fibrosis via regulating Smad3 acetylation.

Kim S, Lim JH, Woo CH.

Am J Pathol. 2013 Dec;183(6):1758-68. doi: 10.1016/j.ajpath.2013.08.014. Epub 2013 Oct 1.

PMID:
24095924
18.

4-Phenylbutyric acid treatment rescues trafficking and processing of a mutant surfactant protein-C.

Stewart GA, Ridsdale R, Martin EP, Na CL, Xu Y, Mandapaka K, Weaver TE.

Am J Respir Cell Mol Biol. 2012 Sep;47(3):324-31. doi: 10.1165/rcmb.2012-0003OC. Epub 2012 Mar 29.

19.

Endoplasmic reticulum stress induced by surfactant protein C BRICHOS mutants promotes proinflammatory signaling by epithelial cells.

Maguire JA, Mulugeta S, Beers MF.

Am J Respir Cell Mol Biol. 2011 Mar;44(3):404-14. doi: 10.1165/rcmb.2009-0382OC. Epub 2010 May 12.

20.

Dissociation of transforming growth factors β1 and β2 from surfactant protein A (SP-A) by deglycosylation or deoxycholate treatment.

Willems CH, Kloosterboer N, Kunzmann S, Kramer BW, Zimmermann LJ, van Iwaarden JF.

J Immunol Methods. 2012 Jan 31;375(1-2):111-7. doi: 10.1016/j.jim.2011.09.014. Epub 2011 Oct 2.

PMID:
21989137

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