Fibroblast growth factors 1, 2, 17, and 19 are the predominant FGF ligands expressed in human fetal growth plate cartilage

被引:53
作者
Krejci, Pavel
Krakow, Deborah
Mekikian, Pertchoui B.
Wilcox, William R.
机构
[1] Cedars Sinai Med Ctr, Med Genet Inst, Los Angeles, CA 90048 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Pediat, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USA
关键词
D O I
10.1203/pdr.0b013e318030d157
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Fibroblast growth factors (FGF) regulate bone growth, but their expression in human cartilage is unclear. Here, we determined the expression of entire FGF family in human fetal growth plate cartilage. Using reverse transcriptase PCR, the transcripts for FGFI, 2, 5. 8-14 16-19, and 21 were found. However, only FGFI, 2, 17, and 19 were detectable at the protein level. By immunohistochemistry, FGF17 and 19 were uniformly expressed within the growth plate. In contrast, FGF1 was found only in proliferating and hypertrophic chondrocytes whereas FGF2 localized predominantly to the resting and proliferating cartilage. In addition, only the 18 kD isoform of FGF2 was found in resting chondrocytes while proliferating chondrocytes also synthesized 22 kD and 24 kD FGF2, similar to in vitro cultivated chondrocytes. In cell growth experiments, FGFI, 2, and 17 but not FGF19 inhibited the proliferation of FGFR3-expressing rat chondrosarcoma chondrocytes (RCS) with relative potency FGF2 >> FGF1 = FGF17. We conclude that FGF1, 2, 17, and 19 are the predominant FGF ligands present in developing human cartilage that are, with the exception of FGF19, experimentally capable of inhibiting chondrocyte proliferation.
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页码:267 / 272
页数:6
相关论文
共 33 条
[1]   Nuclear activities of basic fibroblast growth factor: Potentiation of low-serum growth mediated by natural or chimeric nuclear localization signals [J].
Arese, M ;
Chen, Y ;
Florkiewicz, RZ ;
Gualandris, A ;
Shen, B ;
Rifkin, DB .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (05) :1429-1444
[2]   ALTERNATIVE INITIATION OF TRANSLATION DETERMINES CYTOPLASMIC OR NUCLEAR-LOCALIZATION OF BASIC FIBROBLAST GROWTH-FACTOR [J].
BUGLER, B ;
AMALRIC, F ;
PRATS, H .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (01) :573-577
[3]   Gly369Cys mutation in mouse FGFR3 causes achondroplasia by affecting both chondrogenesis and osteogenesis [J].
Chen, L ;
Adar, R ;
Yang, X ;
Monsonego, EO ;
Li, CL ;
Hauschka, PV ;
Yayon, A ;
Deng, CX .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (11) :1517-1525
[4]   ABNORMAL BONE-GROWTH AND SELECTIVE TRANSLATIONAL REGULATION IN BASIC FIBROBLAST GROWTH-FACTOR (FGF-2) TRANSGENIC MICE [J].
COFFIN, JD ;
FLORKIEWICZ, RZ ;
NEUMANN, J ;
MORTHOPKINS, T ;
DORN, GW ;
LIGHTFOOT, P ;
GERMAN, R ;
HOWLES, PN ;
KIER, A ;
OTOOLE, BA ;
SASSE, J ;
GONZALEZ, AM ;
BAIRD, A ;
DOETSCHMAN, T .
MOLECULAR BIOLOGY OF THE CELL, 1995, 6 (12) :1861-1873
[5]   Spatio-temporal expression of FGFR 1, 2 and 3 genes during human embryo-fetal ossification [J].
Delezoide, AL ;
Benoist-Lasselin, C ;
Legeai-Mallet, L ;
Le Merrer, M ;
Munnich, A ;
Vekemans, M ;
Bonaventure, J .
MECHANISMS OF DEVELOPMENT, 1998, 77 (01) :19-30
[6]   Overexpression of the FGF-2 24-kDa isoform up-regulates IL-6 transcription in NIH-3T3 cells [J].
Delrieu, I ;
Arnaud, E ;
Ferjoux, G ;
Bayard, F ;
Faye, JC .
FEBS LETTERS, 1998, 436 (01) :17-22
[7]   Fibroblast growth factor receptor 3 is a negative regulator of bone growth [J].
Deng, CX ;
WynshawBoris, A ;
Zhou, F ;
Kuo, A ;
Leder, P .
CELL, 1996, 84 (06) :911-921
[8]  
ESTIVAL A, 1993, CANCER RES, V53, P1182
[9]   Distribution of fibroblast growth factor (FGF)-2 and FGF receptor-1 messenger RNA expression and protein presence in the mid-trimester human fetus [J].
Gonzalez, AM ;
Hill, DJ ;
Logan, A ;
Maher, PA ;
Baird, A .
PEDIATRIC RESEARCH, 1996, 39 (03) :375-385
[10]   ADAPTATIONS OF GOLDNER MASSON TRICHROME STAIN FOR THE STUDY OF UNDECALCIFIED PLASTIC EMBEDDED BONE [J].
GRUBER, HE .
BIOTECHNIC & HISTOCHEMISTRY, 1992, 67 (01) :30-34