The Role of Glycoprotein 130 Family of Cytokines in Fetal Rat Lung Development

被引:16
作者
Nogueira-Silva, Cristina [1 ,2 ,3 ]
Piairo, Paulina [1 ,2 ]
Carvalho-Dias, Emanuel [1 ,2 ,4 ]
Veiga, Carla [1 ,2 ]
Moura, Rute S. [1 ,2 ]
Correia-Pinto, Jorge [1 ,2 ,5 ]
机构
[1] Univ Minho, Life & Hlth Sci Res Inst, Sch Hlth Sci, Braga, Portugal
[2] 3Bs PT Govt Associate Lab, Life & Hlth Sci Res Inst, Braga, Portugal
[3] Hosp Braga, Dept Obstet & Gynecol, Braga, Portugal
[4] Hosp Braga, Dept Urol, Braga, Portugal
[5] Hosp Braga, Dept Pediat Surg, Braga, Portugal
来源
PLOS ONE | 2013年 / 8卷 / 06期
关键词
RECOMBINANT HUMAN INTERLEUKIN-11; CILIARY NEUROTROPHIC FACTOR; PROGRAMMED CELL-DEATH; ONCOSTATIN-M; BRANCHING MORPHOGENESIS; FACTOR CNTF; EXPRESSION; GP130; CARDIOTROPHIN-1; MECHANISMS;
D O I
10.1371/journal.pone.0067607
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The glycoprotein 130 (gp130) dependent family of cytokines comprises interleukin-6 (IL-6), IL-11, leukemia inhibitory factor (LIF), cardiotrophin-like cytokine (CLC), ciliary neurotrophic factor (CNTF), cardiotrophin-1 (CT-1) and oncostatin M (OSM). These cytokines share the membrane gp130 as a common signal transducer. Recently, it was demonstrated that IL-6 promotes, whereas LIF inhibits fetal lung branching. Thus, in this study, the effects on fetal lung morphogenesis of the other classical members of the gp130-type cytokines (IL-11, CLC, CNTF, CT-1 and OSM) were investigated. We also provide the first description of these cytokines and their common gp130 receptor protein expression patterns during rat lung development. Fetal rat lung explants were cultured in vitro with increasing concentrations of IL-11, CLC, CNTF, CT-1 and OSM. Treated lung explants were morphometrically analyzed and assessed for MAPK, PI3K/AKT and STAT3 signaling modifications. IL-11, which similarly to IL-6 acts through a gp130 homodimer receptor, significantly stimulated lung growth via p38 phosphorylation. On the other hand, CLC, CNTF, CT-1 and OSM, whose receptors are gp130 heterodimers, inhibited lung growth acting in different signal-transducing pathways. Thus, the present study demonstrated that although cytokines of the gp130 family share a common signal transducer, there are specific biological activities for each cytokine on lung development. Indeed, cytokine signaling through gp130 homodimers stimulate, whereas cytokine signaling through gp130 heterodimers inhibit lung branching.
引用
收藏
页数:15
相关论文
共 55 条
[1]   Postnatally induced inactivation of gp130 in mice results in neurological, cardiac, hematopoietic, immunological, hepatic, and pulmonary defects [J].
Betz, UAK ;
Bloch, W ;
van den Broek, M ;
Yoshida, K ;
Taga, T ;
Kishimoto, T ;
Addicks, K ;
Rajewsky, K ;
Müller, W .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (10) :1955-1965
[2]   Intracellular proteins and mechanisms involved in the control of gp130/JAK/STAT cytokine signaling [J].
Carbia-Nagashima, A ;
Arzt, E .
IUBMB LIFE, 2004, 56 (02) :83-88
[3]   Effects of the gp130 cytokines ciliary neurotropic factor (CNTF) and interleukin-11 on pituitary cells: CNTF receptors on human pituitary adenomas and stimulation of prolactin and GH secretion in normal rat anterior pituitary aggregate cultures [J].
Castro, CP ;
Nagashima, AC ;
Pereda, MP ;
Goldberg, V ;
Chervin, A ;
Carrizo, G ;
Molina, H ;
Renner, U ;
Stalla, GK ;
Arzt, E .
JOURNAL OF ENDOCRINOLOGY, 2001, 169 (03) :539-547
[4]   SOCS regulation of the JAK/STAT signalling pathway [J].
Croker, Ben A. ;
Kiu, Hiu ;
Nicholson, Sandra E. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2008, 19 (04) :414-422
[5]   clc is co-expressed with clf or cntfr in developing mouse muscles [J].
de Bovis B. ;
Derouet D. ;
Gauchat J.-F. ;
Elson G. ;
Gascan H. ;
deLapeyrière O. .
Cell Communication and Signaling, 3 (1)
[6]   Optimizing neurotrophic factor combinations for neurite outgrowth [J].
Deister, C. ;
Schmidt, C. E. .
JOURNAL OF NEURAL ENGINEERING, 2006, 3 (02) :172-179
[7]   Recombinant human interleukin-11 prevents mucosal atrophy and bowel shortening in the defunctionalized intestine [J].
Dickinson, EC ;
Tuncer, R ;
Nadler, EP ;
Koltuksuz, U ;
Boyle, P ;
Alber, SM ;
Watkins, SC ;
Ford, HR .
JOURNAL OF PEDIATRIC SURGERY, 2000, 35 (07) :1079-1083
[8]  
Du XX, 1996, J CELL PHYSIOL, V168, P362
[9]   Conditional gp130 deficient mouse mutants [J].
Fasnacht, Nicolas ;
Mueller, Werner .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2008, 19 (04) :379-384
[10]   Glycoprotein 130 Cytokine Signal as a Therapeutic Target Against Cardiovascular Diseases [J].
Fujio, Yasushi ;
Maeda, Makiko ;
Mohri, Tomomi ;
Obana, Masanori ;
Iwakura, Tomohiko ;
Hayama, Akiko ;
Yamashita, Tomomi ;
Nakayama, Hiroyuki ;
Azuma, Junichi .
JOURNAL OF PHARMACOLOGICAL SCIENCES, 2011, 117 (04) :213-222