Retinoic Aacid Diminished the Expression of MMP-2 in Hyperoxia-exposed Premature Rat Lung Fibroblasts through Regulating Mitogen-activated Protein Kinases
This study examined the effects of retinoic acid (RA), PD98059, SP600125 and SB203580 on the hyperoxia-induced expression and regulation of matrix metalloproteinase-2 (MMP-2) and metalloproteinase-2 (TIMP-2) in premature rat lung fibroblasts (LFs). LFs were exposed to hyperoxia or room air for 12 h...
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Published in | Journal of Huazhong University of Science and Technology. Medical sciences Vol. 31; no. 2; pp. 251 - 257 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Heidelberg
Huazhong University of Science and Technology
01.04.2011
Department of Pediatrics, Tongji Hospital, Tongji Medical University, Huazhong University of Science and Technology, Wuhan 430030, China |
Subjects | |
Online Access | Get full text |
ISSN | 1672-0733 1993-1352 |
DOI | 10.1007/s11596-011-0262-1 |
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Abstract | This study examined the effects of retinoic acid (RA), PD98059, SP600125 and SB203580 on the hyperoxia-induced expression and regulation of matrix metalloproteinase-2 (MMP-2) and metalloproteinase-2 (TIMP-2) in premature rat lung fibroblasts (LFs). LFs were exposed to hyperoxia or room air for 12 h in the presence of RA and the kinase inhibitors PD98059 (ERK1/2), SP600125 (JNK1/2) and SB203580 (p38) respectively. The expression levels of MMP-2 and TIMP-2 mRNA were detected by semi-quantitative reverse transcription polymerase chain reaction (RT-PCR). MMP-2 activity was measured by zymography. The amount of p-ERK1/2, REK1/2, p-JNK1/2, JNK1/2, p-p38 and p38 was determined by Western blotting. The results showed that: (1) PD98059, SP600125 and SB203580 significantly inhibited p-ERK1/2, p-JNK1/2 and p-p38 respectively in LFs; (2) The expression of MMP-2 mRNA in LFs exposed to hyperoxia was decreased after treatment with RA, SP600125 and SB203580 respectively (P0.01 or 0.05), but did not change after treatment with PD98059 (P0.05). Meanwhile, RA, PD98059, SP600125 and SB203580 had no effect on the expression of TIMP-2 mRNA in LFs exposed to room air or hyperoxia (P0.05); (3) The expression of pro- and active MMP-2 experienced no change after treatment with RA or SP600125 in LFs exposed to room air (P0.05), but decreased remarkably after hyperoxia (P0.01 or 0.05). SB203580 inhibited the expression of pro- and active MMP-2 either in room air or under hyperoxia (P0.01). PD98059 exerted no effect on the expression of pro- and active MMP-2 (P0.05). It was suggested that RA had a protective effect on hyperoxia-induced lung injury by down-regulating the expression of MMP-2 through decreasing the JNK and p38 activation in hyperoxia. |
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AbstractList | This study examined the effects of retinoic acid (RA), PD98059, SP600125 and SB203580 on the hyperoxia-induced expression and regulation of matrix metalloproteinase-2 (MMP-2) and metalloproteinase-2 (TIMP-2) in premature rat lung fibroblasts (LFs). LFs were exposed to hyperoxia or room air for 12 h in the presence of RA and the kinase inhibitors PD98059 (ERK1/2), SP600125 (JNK1/2) and SB203580 (p38) respectively. The expression levels of MMP-2 and TIMP-2 mRNA were detected by semi-quantitative reverse transcription polymerase chain reaction (RT-PCR). MMP-2 activity was measured by zymography. The amount of p-ERK1/2, REK1/2, p-JNK1/2, JNK1/2, p-p38 and p38 was determined by Western blotting. The results showed that: (1) PD98059, SP600125 and SB203580 significantly inhibited p-ERK1/2, p-JNK1/2 and p-p38 respectively in LFs; (2) The expression of MMP-2 mRNA in LFs exposed to hyperoxia was decreased after treatment with RA, SP600125 and SB203580 respectively (P0.01 or 0.05), but did not change after treatment with PD98059 (P0.05). Meanwhile, RA, PD98059, SP600125 and SB203580 had no effect on the expression of TIMP-2 mRNA in LFs exposed to room air or hyperoxia (P0.05); (3) The expression of pro- and active MMP-2 experienced no change after treatment with RA or SP600125 in LFs exposed to room air (P0.05), but decreased remarkably after hyperoxia (P0.01 or 0.05). SB203580 inhibited the expression of pro- and active MMP-2 either in room air or under hyperoxia (P0.01). PD98059 exerted no effect on the expression of pro- and active MMP-2 (P0.05). It was suggested that RA had a protective effect on hyperoxia-induced lung injury by down-regulating the expression of MMP-2 through decreasing the JNK and p38 activation in hyperoxia. R563; This study examined the effects of retinoic acid (RA),PD98059,SP600125 and SB203580 on the hyperoxia-induced expression and regulation of matrixmetalloproteinase-2 (MMP-2) and metalloproteinase-2 (TIMP-2) in premature rat lung fibroblasts (LFs).LFs were exposed to hyperoxia or room air for 12 h in the presence of RA and the kinase inhibitors PD98059 (ERK1/2),SP600125 (JNK1/2) and SB203580 (p38) respectively.The expression levels of MMP-2 and TIMP-2 mRNA were detected by semi-quantitative reverse transcription polymerase chain reaction (RT-PCR).MMP-2 activity was measured by zymography.The amount of p-ERK1/2,REK1/2,p-JNK1/2,JNK1/2,p-p38 and p38 was determined by Western blotting.The results showed that:(1) PD98059,SP600125 and SB203580 significantly inhibited p-ERK1/2,p-JNK1/2 and p-p38 respectively in LFs; (2) The expression of MMP-2 mRNA in LFs exposed to hyperoxia was decreased after treatment with RA,SP600125 and SB203580 respectively (P<0.01 or 0.05),but did not change after treatment with PD98059 (P>0.05).Meanwhile,RA,PD98059,SP600125 and SB203580 had no effect on the expression of TIMP-2 mRNA in LFs exposed to room air or hyperoxia (P>0.05); (3) The expression of pro- and active MMP-2 experienced no change after treatment with RA or SP600125 in LFs exposed to room air (P>0.05),but decreased remarkably after hyperoxia (P<0.01 or 0.05).SB203580 inhibited the expression of pro- and active MMP-2 either in room air or under hyperoxia (P<0.01).PD98059 exerted no effect on the expression of pro- and active MMP-2 (P<0.05).It was suggested that RA had a protective effect on hyperoxia-induced lung injury by down-regulating the expression of MMP-2 through decreasing the JNK and p38 activation in hyperoxia. Summary This study examined the effects of retinoic acid (RA), PD98059, SP600125 and SB203580 on the hyperoxia-induced expression and regulation of matrix metalloproteinase-2 (MMP-2) and metalloproteinase-2 (TIMP-2) in premature rat lung fibroblasts (LFs). LFs were exposed to hyperoxia or room air for 12 h in the presence of RA and the kinase inhibitors PD98059 (ERK1/2), SP600125 (JNK1/2) and SB203580 (p38) respectively. The expression levels of MMP-2 and TIMP-2 mRNA were detected by semi-quantitative reverse transcription polymerase chain reaction (RT-PCR). MMP-2 activity was measured by zymography. The amount of p-ERK1/2, REK1/2, p-JNK1/2, JNK1/2, p-p38 and p38 was determined by Western blotting. The results showed that: (1) PD98059, SP600125 and SB203580 significantly inhibited p-ERK1/2, p-JNK1/2 and p-p38 respectively in LFs; (2) The expression of MMP-2 mRNA in LFs exposed to hyperoxia was decreased after treatment with RA, SP600125 and SB203580 respectively ( P <0.01 or 0.05), but did not change after treatment with PD98059 ( P >0.05). Meanwhile, RA, PD98059, SP600125 and SB203580 had no effect on the expression of TIMP-2 mRNA in LFs exposed to room air or hyperoxia ( P >0.05); (3) The expression of pro- and active MMP-2 experienced no change after treatment with RA or SP600125 in LFs exposed to room air ( P >0.05), but decreased remarkably after hyperoxia ( P <0.01 or 0.05). SB203580 inhibited the expression of pro- and active MMP-2 either in room air or under hyperoxia ( P <0.01). PD98059 exerted no effect on the expression of pro- and active MMP-2 ( P <0.05). It was suggested that RA had a protective effect on hyperoxia-induced lung injury by down-regulating the expression of MMP-2 through decreasing the JNK and p38 activation in hyperoxia. |
Author | 李文斌 常立文 容志惠 刘伟 |
AuthorAffiliation | Department of Pediatrics, Tongji Hospital, Tongji Medical University, Huazhong University of Science and Technology, Iguhan 430030, China |
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CitedBy_id | crossref_primary_10_3389_fncel_2015_00305 crossref_primary_10_1016_j_resp_2014_12_002 crossref_primary_10_3390_antiox12030548 crossref_primary_10_1111_aji_12787 crossref_primary_10_4062_biomolther_2012_20_2_133 crossref_primary_10_1155_2020_3123968 crossref_primary_10_3390_ijms242317038 |
Cites_doi | 10.1158/0008-5472.CAN-09-2918 10.1002/ppul.20131 10.1152/ajplung.00441.2007 10.1126/science.1072682 10.1074/jbc.M407383200 10.1016/S0002-9440(10)65625-8 10.1067/mpd.2003.214 10.1074/jbc.273.12.7066 10.1203/PDR.0b013e318193f165 10.1186/rr33 10.1016/j.ydbio.2004.09.033 10.1016/S0022-3476(05)81800-1 10.1074/jbc.M301624200 10.1111/j.1651-2227.1997.tb14897.x 10.1152/japplphysiol.01392.2009 10.2741/3179 10.1074/jbc.M204296200 10.1074/jbc.M109801200 10.1152/ajplung.00200.2001 10.1152/ajplung.00387.2002 10.1074/jbc.M100199200 10.1165/ajrcmb.25.2.4362 10.4049/jimmunol.165.10.5788 10.1242/jcs.115.4.839 |
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Notes | 42-1679/R This study examined the effects of retinoic acid (RA), PD98059, SP600125 and SB203580 on the hyperoxia-induced expression and regulation of matrix metalloproteinase-2 (MMP-2) and metalloproteinase-2 (TIMP-2) in premature rat lung fibroblasts (LFs). LFs were exposed to hyperoxia or room air for 12 h in the presence of RA and the kinase inhibitors PD98059 (ERK1/2), SP600125 (JNK1/2) and SB203580 (p38) respectively. The expression levels of MMP-2 and TIMP-2 mRNA were detected by semi-quantitative reverse transcription polymerase chain reaction (RT-PCR). MMP-2 activity was measured by zymography. The amount of p-ERK1/2, REK1/2, p-JNK1/2, JNK1/2, p-p38 and p38 was determined by Western blotting. The results showed that: (1) PD98059, SP600125 and SB203580 significantly inhibited p-ERK1/2, p-JNK1/2 and p-p38 respectively in LFs; (2) The expression of MMP-2 mRNA in LFs exposed to hyperoxia was decreased after treatment with RA, SP600125 and SB203580 respectively (P0.01 or 0.05), but did not change after treatment with PD98059 (P0.05). Meanwhile, RA, PD98059, SP600125 and SB203580 had no effect on the expression of TIMP-2 mRNA in LFs exposed to room air or hyperoxia (P0.05); (3) The expression of pro- and active MMP-2 experienced no change after treatment with RA or SP600125 in LFs exposed to room air (P0.05), but decreased remarkably after hyperoxia (P0.01 or 0.05). SB203580 inhibited the expression of pro- and active MMP-2 either in room air or under hyperoxia (P0.01). PD98059 exerted no effect on the expression of pro- and active MMP-2 (P0.05). It was suggested that RA had a protective effect on hyperoxia-induced lung injury by down-regulating the expression of MMP-2 through decreasing the JNK and p38 activation in hyperoxia. Wenbin LI, Liwen CHANG#, Zhihui RONG, Wei LIU Department of Pediatrics, Tongji Hospital, Tongji Medical University, Huazhong University of Science and Technology, Wuhan 430030, China hyperoxia; retinoic acid; lung fibroblasts; premature rats; matrix metalloproteinase-2; mitogen-activated protein kinases |
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PublicationTitle | Journal of Huazhong University of Science and Technology. Medical sciences |
PublicationTitleAbbrev | J. Huazhong Univ. Sci. Technol. [Med. Sci.] |
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SubjectTerms | Medicine Medicine & Public Health MMP PD98059 半定量逆转录聚合酶链反应 基质金属蛋白酶-2 有丝分裂原活化蛋白激酶 维甲酸 肺成纤维细胞 高氧 |
Title | Retinoic Aacid Diminished the Expression of MMP-2 in Hyperoxia-exposed Premature Rat Lung Fibroblasts through Regulating Mitogen-activated Protein Kinases |
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