Suppression of differentiation and proliferation of early chondrogenic cells by Notch

被引:110
作者
Watanabe, N
Tezuka, Y
Matsuno, K
Miyatani, S
Morimura, N
Yasuda, M
Fujimaki, R
Kuroda, K
Hiraki, Y
Hozumi, N
Tezuka, K
机构
[1] Gifu Univ, Grad Sch Med, Dept Tissue & Organ Dev REgenerat & Adv Med Sci, Gifu 5008705, Japan
[2] Tokyo Univ Sci, Res Inst Biol Sci, Noda, Chiba 278, Japan
[3] Tokyo Univ Sci, Dept Biol Sci & Technol, Noda, Chiba 278, Japan
[4] RIKEN, Inst Phys & Chem Res, Wako, Saitama 35101, Japan
[5] Keio Univ, Sch Med, Dept Orthopaed Surg, Tokyo, Japan
[6] Kyoto Univ, Fac Med, Dept Med Chem, Kyoto 606, Japan
[7] Kyoto Univ, Inst Frontier Med Sci, Kyoto, Japan
关键词
Notch; chondrocyte; perichondrium; ATDC5; Deltex;
D O I
10.1007/s00774-003-0428-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Notch is a transmembrane protein involved in cell fate determination. In the present study, we observed temporally and spatially restricted expression of Notch1 in developing cartilage. Notch1 was localized starting from the mesenchymal condensation stage of embryonic mouse forelimbs. Interestingly, although localization could not be detected in the proliferating chondrocytes, obvious immunoreactivity indicating its expression was retained in the perichondrial region. Next, we investigated the expression of Notch1 and related molecules in a chondrogenic cell line, ATDC5 cells. Notch1, Delta-like (Dll)1, Deltex2, and Deltex3 were coexpressed after 6-day insulin treatment. Expression of Hairy and Enhancer of split homologue (HES)-1 followed thereafter. These results suggest that Notch may have a role in the early stage of chondrogenesis. To assess the effect of Notch activation, we cultured ATDC5 cells with a myeloma clone constitutively expressing D111, a ligand of Notch. We also used an adenovirus vector to express the constitutively active Notch1 intracellular domain (NIC). Activating either the endogenous or exogenous Notch receptor dramatically inhibited chondrogenic cell differentiation of ATDC5 cells, as assessed by Alcian blue staining of the cells and chondrocyte differentiation markers. Last, we investigated the effect of NIC on the proliferation of the ATDC5 cells. Expression of NIC by the adenovirus strongly suppressed thymidine incorporation. These results indicate that Notch is expressed in the initial stage of chondrogenic cell differentiation and has a strong inhibitory effect on both differentiation and proliferation of the cells when activated. The expression of Notch decreases as chondrogenic differentiation proceeds; however, a population of the cells with sustained expression of Notch1 become perichondrial cells. Considering that the perichondrium acts as a stern cell source of osteoblasts and chondrocytes, Notch1 may have a role in the formation of these cells by suppressing both differentiation and proliferation.
引用
收藏
页码:344 / 352
页数:9
相关论文
共 31 条
[11]   Defects in limb, craniofacial, and thymic development in Jagged2 mutant mice [J].
Jiang, RL ;
Lan, Y ;
Chapman, HD ;
Shawber, C ;
Norton, CR ;
Serreze, DV ;
Weinmaster, G ;
Gridley, T .
GENES & DEVELOPMENT, 1998, 12 (07) :1046-1057
[12]   EFFICIENT GENE ACTIVATION IN MAMMALIAN-CELLS BY USING RECOMBINANT ADENOVIRUS EXPRESSING SITE-SPECIFIC CRE RECOMBINASE [J].
KANEGAE, Y ;
LEE, G ;
SATO, Y ;
TANAKA, M ;
NAKAI, M ;
SAKAKI, T ;
SUGANO, S ;
SAITO, I .
NUCLEIC ACIDS RESEARCH, 1995, 23 (19) :3816-3821
[13]   A role for Pref-1 and HES-1 in thymocyte development [J].
Kaneta, M ;
Osawa, M ;
Osawa, M ;
Sudo, K ;
Nakauchi, H ;
Farr, AG ;
Takahama, Y .
JOURNAL OF IMMUNOLOGY, 2000, 164 (01) :256-264
[14]  
Koizumi K, 2001, DEVELOPMENT, V128, P1391
[15]   Delta-induced notch signaling mediated by RBP-J inhibits MyoD expression and myogenesis [J].
Kuroda, K ;
Tani, S ;
Tamura, K ;
Minoguchi, S ;
Kurooka, H ;
Honjo, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (11) :7238-7244
[16]   Notch signalling pathway mediates hair cell development in mammalian cochlea [J].
Lanford, PJ ;
Lan, Y ;
Jiang, RL ;
Lindsell, C ;
Weinmaster, G ;
Gridley, T ;
Kelley, MW .
NATURE GENETICS, 1999, 21 (03) :289-292
[17]   Identification of an enhancer sequence within the first intron required for cartilage-specific transcription of the α2(XI) collagen gene [J].
Liu, Y ;
Li, HC ;
Tanaka, K ;
Tsumaki, N ;
Yamada, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (17) :12712-12718
[18]   Efficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome [J].
Miyake, S ;
Makimura, M ;
Kanegae, Y ;
Harada, S ;
Sato, Y ;
Takamori, K ;
Tokuda, C ;
Saito, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (03) :1320-1324
[19]   Cell cycle arrest and apoptosis induced by Notch1 in B cells [J].
Morimura, T ;
Goitsuka, R ;
Zhang, Y ;
Saito, I ;
Reth, M ;
Kitamura, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (47) :36523-36531
[20]  
OKA C, 1995, DEVELOPMENT, V121, P3291