Spatio-temporal expression patterns of Runx2 isoforms in early skeletogenesis

被引:44
作者
Choi, KY
Lee, SW
Park, MH
Bae, YC
Shin, HI
Nam, SH
Kim, YJ
Kim, HJ
Ryoo, HM [1 ]
机构
[1] Kyungpook Natl Univ, Sch Dent, Dept Pediat Dent, Taejon, South Korea
[2] Kyungpook Natl Univ, Sch Dent, Dept Biochem, Taejon, South Korea
[3] Kyungpook Natl Univ, Sch Dent, Dept Oral Hist, Taejon, South Korea
[4] Kyungpook Natl Univ, Sch Dent, Dept Oral Pathol, Taejon, South Korea
关键词
chondrocytes; chondrogenesis; collagen type-II; osteoblasts; osteogenesis; transcription factors;
D O I
10.1038/emm.2002.60
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Skeletogenesis occurs through either intramembranous or endochondral ossification. In addition some parts of the skeletal components maintain their cartilaginous characteristics throughout life without mineralization. Runx2 is known to be a pivotal transcription factor for all skeletogenic processes. In this study, we examined the expression patterns of two major isoforms of Runx2 in early skeletogenesis. During intramembranous bone formation, Runx2-type I (Runx2-I) was widely expressed in osteoprogenitor cells and active osteoblasts, while Runx2-type II (Runx2-II) expression was stringently restricted to cells lining mineralized bones. Cells in permanent cartilage expressed collagen type II (Col-II) but never expressed Runx2 or Col-X. These permanent cartilages were well circumscribed by Runx2-I positive cells, in which Runx2-II was negative. In endochondral bone formation, Runx2 expression temporarily disappeared in Col-II-positive proliferating chondrocytes, but a secondary surge of Runx2-I expression occurred in the prehypertrophic zone before the mineralization of cartilage. Collectively, both Runx2 isoforms showed very similar expression patterns in active bone forming areas; however, Runx2-I has an exclusive role in the early commitment stage of intramembranous or endochondral bone forming processes or in cells surrounding permanent cartilage.
引用
收藏
页码:426 / 433
页数:8
相关论文
共 19 条
  • [1] The RUNX3 gene -: sequence, structure and regulated expression
    Bangsow, C
    Rubins, N
    Glusman, G
    Bernstein, Y
    Negreanu, V
    Goldenberg, D
    Lotem, J
    Ben-Asher, E
    Lancet, D
    Levanon, D
    Groner, Y
    [J]. GENE, 2001, 279 (02) : 221 - 232
  • [2] Sox9 is required for cartilage formation
    Bi, WM
    Deng, JM
    Zhang, ZP
    Behringer, RR
    de Crombrugghe, B
    [J]. NATURE GENETICS, 1999, 22 (01) : 85 - 89
  • [3] Osf2/Cbfa1: A transcriptional activator of osteoblast differentiation
    Ducy, P
    Zhang, R
    Geoffroy, V
    Ridall, AL
    Karsenty, G
    [J]. CELL, 1997, 89 (05) : 747 - 754
  • [4] Cbfa1 isoforms exert functional differences in osteoblast differentiation
    Harada, H
    Tagashira, S
    Fujiwara, M
    Ogawa, S
    Katsumata, T
    Yamaguchi, A
    Komori, T
    Nakatsuka, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (11) : 6972 - 6978
  • [5] Inada M, 1999, DEV DYNAM, V214, P279, DOI 10.1002/(SICI)1097-0177(199904)214:4<279::AID-AJA1>3.0.CO
  • [6] 2-W
  • [7] Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts
    Komori, T
    Yagi, H
    Nomura, S
    Yamaguchi, A
    Sasaki, K
    Deguchi, K
    Shimizu, Y
    Bronson, RT
    Gao, YH
    Inada, M
    Sato, M
    Okamoto, R
    Kitamura, Y
    Yoshiki, S
    Kishimoto, T
    [J]. CELL, 1997, 89 (05) : 755 - 764
  • [8] Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1
    Levanon, D
    Glusman, C
    Bangsow, T
    Ben-Asher, E
    Male, DA
    Avidan, N
    Bangsow, C
    Hattori, M
    Taylor, TD
    Taudien, S
    Blechschmidt, K
    Shimizu, N
    Rosenthal, A
    Sakaki, Y
    Lancet, D
    Groner, Y
    [J]. GENE, 2001, 262 (1-2) : 23 - 33
  • [9] MARKS SC, 1997, PRINCIPLES BONE BIOL, P3
  • [10] SEQUENCE SPECIFICITY OF THE CORE-BINDING FACTOR
    MELNIKOVA, IN
    CRUTE, BE
    WANG, SW
    SPECK, NA
    [J]. JOURNAL OF VIROLOGY, 1993, 67 (04) : 2408 - 2411