In situ expression of 15 kDa interferon alpha responsive gene in the developing tooth germ of the mouse lower first molar

被引:7
作者
Akhter, Merina [1 ,2 ]
Kobayashi, Ieyoshi [1 ]
Kiyoshima, Tamotsu [1 ]
Nagata, Kengo [1 ]
Wada, Hiroko [1 ]
Ookuma, Yukiko [1 ,3 ]
Fujiwara, Hiroaki [1 ]
Honda, Jyun-ya [1 ,4 ]
Sakai, Hidetaka [1 ]
机构
[1] Kyushu Univ, Lab Oral & Pathol & Med, Div Maxillofacial Diagnost & Surg Sci, Fac Dent Sci,Higashi Ku, Fukuoka 8128582, Japan
[2] Rangpur Dent Coll, Dept Oral Pathol Periodontol & Oral Med, Med E Gate 5400, Rangpur, Bangladesh
[3] Kyushu Univ, Sect Pediat Dent, Div Oral Hlth Growth & Dev, Fac Dent Sci,Higashi Ku, Fukuoka 8128582, Japan
[4] Kyushu Univ, Dept Orthodont, Div Oral Hlth Growth & Dev, Fac Dent Sci,Higashi Ku, Fukuoka 8128582, Japan
关键词
Interferon alpha responsive protein; Ifrg15; Tooth germ development; In situ hybridization; DER-WOUDE-SYNDROME; LOWER; 1ST-MOLAR; HUMAN-CELLS; APOPTOSIS; EMBRYOS; VAN; PATHWAY; CLONING; FGF-4; IRF6;
D O I
10.1007/s10735-010-9277-3
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
We previously performed cDNA subtraction between the mouse mandibles at embryonic day 10.5 (E10.5) and E12.0 to make a profile of the regulator genes for odontogenesis. Fifteen kDa interferon alpha responsive gene (Ifrg15) is one of several highly-expressed genes in the E12.0 mandible. The current study examined the precise expression patterns of Ifrg15 mRNA in the mouse mandibular first molar by in situ hybridization to evaluate the possible functional roles of this gene in odontogenesis. Ifrg15 mRNA was expressed in the epithelial and mesenchymal tissues of the mandible at E10.5 and E12.0. The Ifrg15 in situ signal was detected in the epithelial bud and the surrounding mesenchyme at E14.0, and was present in the enamel organ including the primary enamel knot, and in the underlying mesenchyme at E15.0. The in situ signal was restricted in the inner and outer enamel epithelia and the stratum intermedium at E16.0. The signal of Ifrg15 mRNA was further restricted to the inner enamel epithelium and the adjacent stratum intermedium at E17.0 and E18.0. Consequently, the expression of Ifrg15 mRNA was localized in the ameloblasts and odontoblasts at postnatal days 1.0 to 3.0. However, the in situ signal was markedly weaker than at the embryonic period. The expression of Ifrg15 mRNA was coincidently observed in various craniofacial organs as well as in the tooth germ. These results suggest that Ifrg15 is closely related to odontogenesis, especially the differentiation of the ameloblasts and odontoblasts, and to the morphogenesis of the craniofacial organs.
引用
收藏
页码:185 / 191
页数:7
相关论文
共 33 条
[1]
Possible functional involvement of thymosin beta 4 in developing tooth germ of mouse lower first molar [J].
Akhter, M ;
Kobayashi, I ;
Kiyoshima, T ;
Matsuo, K ;
Yamaza, H ;
Wada, H ;
Honda, JY ;
Ming, X ;
Sakai, H .
HISTOCHEMISTRY AND CELL BIOLOGY, 2005, 124 (3-4) :207-213
[2]
Interferon-α induces apoptosis in human KB cells through a stress-dependent mitogen activated protein kinase pathway that is antagonized by epidermal growth factor [J].
Caraglia, M ;
Abbruzzese, A ;
Leardi, A ;
Pepe, S ;
Budillon, A ;
Baldassare, G ;
Selleri, C ;
De Lorenzo, S ;
Fabbrocini, A ;
Giuberti, G ;
Vitale, G ;
Lupoli, G ;
Bianco, AR ;
Tagliaferri, P .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (08) :773-780
[3]
Identification of genes differentially regulated by interferon α, β, or γ using oligonucleotide arrays [J].
Der, SD ;
Zhou, AM ;
Williams, BRG ;
Silverman, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15623-15628
[4]
DSOUZA RN, 2007, 10 CATES ORAL HISTOL, P79
[5]
DEVELOPMENTAL CONTROL OF IFN-ALPHA EXPRESSION IN MURINE EMBRYOS [J].
DUCGOIRAN, P ;
ROBERT, B ;
NAVARRO, S ;
CIVAS, A ;
CERUTTI, I ;
RUDANT, C ;
MAURY, M ;
CONDAMINE, H ;
DOLY, J .
EXPERIMENTAL CELL RESEARCH, 1994, 214 (02) :570-583
[6]
TRANSCRIPTIONAL AND POSTTRANSCRIPTIONAL REGULATION OF INTERFERON-INDUCED GENE-EXPRESSION IN HUMAN-CELLS [J].
FRIEDMAN, RL ;
MANLY, SP ;
MCMAHON, M ;
KERR, IM ;
STARK, GR .
CELL, 1984, 38 (03) :745-755
[7]
Vanadate facilitates interferon α-mediated apoptosis that is dependent on the Jak/Stat pathway [J].
Gamero, AM ;
Larner, AC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (17) :13547-13553
[8]
Honda JY, 2008, HISTOL HISTOPATHOL, V23, P423, DOI 10.14670/HH-23.423
[9]
JERNVALL J, 1994, INT J DEV BIOL, V38, P463
[10]
Developmental expression analysis of the mouse and chick orthologues of IRF6:: The gene mutated in Van der Woude syndrome [J].
Knight, Alexandra S. ;
Schutte, Brian C. ;
Jiang, Rulang ;
Dixon, Michael J. .
DEVELOPMENTAL DYNAMICS, 2006, 235 (05) :1441-1447