Activation of latent transforming growth factor beta during Chlamydia trachomatis-induced murine pneumonia

被引:14
作者
Williams, DM
Grubbs, BG
ParkSnyder, S
Rank, RG
Bonewald, LF
机构
[1] AUDIE L MURPHY MEM VET ADM MED CTR, DEPT MED, SAN ANTONIO, TX 78284 USA
[2] UNIV ARKANSAS MED SCI HOSP, DEPT MICROBIOL & IMMUNOL, LITTLE ROCK, AR 72205 USA
关键词
cytokine; TGF beta; immunosuppression; Chlamydia trachomatis; RT/PCR; Northern blot; active and latent TGF beta; beta 1 and beta 2 isoforms;
D O I
10.1016/0923-2508(96)81385-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Transforming growth factor beta (TGF beta) is a multifunctional cytokine with potentially important roles in both host defence and immunopathogenesis. Latent, but more importantly, active TGF beta was significantly elevated in bronchiolar lavage fluid from lungs of mice infected with murine Chlamydia trachomatis. Induction of both latent and active TGF beta in these infected animals was highest at day two after infection (2 to 4-fold) compared with day 15 (1 to 2-fold). Both active and latent TGF beta 1 and TGF beta 2 isoforms were detected. Quantitative reverse transcription polymerase chain reaction (RT-PCR) assay showed a slight but significant increase in PCR product for TGF beta 1, but Northern analysis for TGF beta 1 in lung tissue was not significantly different between treatment groups. No significant change was observed for TGF beta 2 mRNA by RT-PCR. The increase in active and latent TGF beta in these lung lavages from mice infected with C. trachomatis appears to be primarily post-transcriptionally regulated.
引用
收藏
页码:251 / 262
页数:12
相关论文
共 47 条
[1]   EXPRESSION AND SECRETION OF TYPE-BETA TRANSFORMING GROWTH-FACTOR BY ACTIVATED HUMAN MACROPHAGES [J].
ASSOIAN, RK ;
FLEURDELYS, BE ;
STEVENSON, HC ;
MILLER, PJ ;
MADTES, DK ;
RAINES, EW ;
ROSS, R ;
SPORN, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (17) :6020-6024
[2]   TRANSFORMING GROWTH-FACTOR-BETA IN LEISHMANIAL INFECTION - A PARASITE ESCAPE MECHANISM [J].
BARRALNETTO, M ;
BARRAL, A ;
BROWNELL, CE ;
SKEIKY, YAW ;
ELLINGSWORTH, LR ;
TWARDZIK, DR ;
REED, SG .
SCIENCE, 1992, 257 (5069) :545-548
[3]   PERSISTENT CHLAMYDIAE - FROM CELL-CULTURE TO A PARADIGM FOR CHLAMYDIAL PATHOGENESIS [J].
BEATTY, WL ;
MORRISON, RP ;
BYRNE, GI .
MICROBIOLOGICAL REVIEWS, 1994, 58 (04) :686-699
[4]   INFECTION OF MURINE MACROPHAGES WITH TOXOPLASMA-GONDII IS ASSOCIATED WITH RELEASE OF TRANSFORMING GROWTH-FACTOR-BETA AND DOWN-REGULATION OF EXPRESSION OF TUMOR-NECROSIS-FACTOR RECEPTORS [J].
BERMUDEZ, LE ;
COVARO, G ;
REMINGTON, J .
INFECTION AND IMMUNITY, 1993, 61 (10) :4126-4130
[5]  
BERMUDEZ LE, 1993, J IMMUNOL, V150, P1838
[6]   ROLE OF ACTIVE AND LATENT TRANSFORMING GROWTH-FACTOR-BETA IN BONE-FORMATION [J].
BONEWALD, LF ;
DALLAS, SL .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, 55 (03) :350-357
[7]   LATENT FORMS OF TRANSFORMING GROWTH-FACTOR-BETA (TGF-BETA) DERIVED FROM BONE CULTURES - IDENTIFICATION OF A NATURALLY-OCCURRING 100-KDA COMPLEX WITH SIMILARITY TO RECOMBINANT LATENT TGF-BETA [J].
BONEWALD, LF ;
WAKEFIELD, L ;
OREFFO, ROC ;
ESCOBEDO, A ;
TWARDZIK, DR ;
MUNDY, GR .
MOLECULAR ENDOCRINOLOGY, 1991, 5 (06) :741-751
[8]   TRANSFORMING GROWTH-FACTOR-BETA IN DISEASE - THE DARK SIDE OF TISSUE-REPAIR [J].
BORDER, WA ;
RUOSLAHTI, E .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (01) :1-7
[9]   NATURAL INHIBITOR OF TRANSFORMING GROWTH-FACTOR-BETA PROTECTS AGAINST SCARRING IN EXPERIMENTAL KIDNEY-DISEASE [J].
BORDER, WA ;
NOBLE, NA ;
YAMAMOTO, T ;
HARPER, JR ;
YAMAGUCHI, Y ;
PIERSCHBACHER, MD ;
RUOSLAHTI, E .
NATURE, 1992, 360 (6402) :361-364
[10]   TRANSFORMING GROWTH FACTOR-BETA-1 IS PRESENT AT SITES OF EXTRACELLULAR-MATRIX GENE-EXPRESSION IN HUMAN PULMONARY FIBROSIS [J].
BROEKELMANN, TJ ;
LIMPER, AH ;
COLBY, TV ;
MCDONALD, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (15) :6642-6646