Abnormal migration and distribution of neural crest cells in Pax6 heterozygous mutant eye, a model for human eye diseases

被引:61
|
作者
Kanakubo, Sachiko
Nomura, Tadashi
Yamamura, Ken-ichi
Miyazaki, Jun-ichi
Tamai, Makoto
Osumi, Noriko
机构
[1] Tohoku Univ, Grad Sch Med, Ctr Translat & Adv Anim Res, Div Dev Neurosci,Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Ophthalmol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[3] Kumamoto Univ, Inst Mol Embryol & Genet, Div Dev Genet, Kumamoto 8620976, Japan
[4] Osaka Univ, Grad Sch Med, Div Stem Cell Regulat Res, Suita, Osaka 5650871, Japan
[5] CREST Japan Sci & Technol Agcy, Kawaguchi 3320012, Japan
关键词
D O I
10.1111/j.1365-2443.2006.00992.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
PAX6/Pax6 gene encodes a transcription factor that is crucially required for eye development. Pax6 heterozygous mutant mouse (Pax6(Sey/+)) shows various ocular defects, especially in the anterior segment. It has been well known that the induction of the lens and development of the cornea and retina are dependent on PAX6/Pax6 in a cell-autonomous fashion, although the influence of PAX6/Pax6 on the other tissues derived from the ocular mesenchyme is largely unknown. Using transgenic mouse lines in which neural crest cells are genetically marked by LacZ or EGFP, we revealed the extensive contribution of neural crest derived cells (NCDCs) to the ocular tissues. Furthermore, various eye defects in Pax6(Sey/+) mouse were accompanied by abnormal distribution of NCDCs from early developmental stages to the adult. In Pax6(Sey/+) mouse mice, neural crest cells abnormally migrated into the developing eye in a cell nonautonomous manner at early embryonic stages. These results indicate that normal distribution and integration of NCDCs in ocular tissues depend on a proper dosage of Pax6, and that Pax6(Sey/+) eye anomalies are caused by cell autonomous and nonautonomous defects due to Pax6 haploinsufficiency.
引用
收藏
页码:919 / 933
页数:15
相关论文
共 35 条
  • [21] A mouse model of aniridia reveals the in vivo downstream targets of Pax6 driving iris and ciliary body development in the eye
    Wang, Xia
    Shan, Xianghong
    Gregory-Evans, Cheryl Y.
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2017, 1863 (01): : 60 - 67
  • [22] Pax6 activity and the expression of FGF8 and BMP4 in neural retina during chick eye development
    Reza, H. M.
    Yasuda, K.
    MECHANISMS OF DEVELOPMENT, 2005, 122 : S92 - S92
  • [23] Down-regulation of Pax6 is associated with abnormal differentiation of corneal epithelial cells in severe ocular surface diseases
    Li, W.
    Chen, Y-T
    Hayashida, Y.
    Blanco, G.
    Kheirkah, A.
    He, H.
    Chen, S-Y
    Liu, C-Y
    Tseng, S. C. G.
    JOURNAL OF PATHOLOGY, 2008, 214 (01): : 114 - 122
  • [24] Molecular changes leading to the abnormal migration of sacral neural crest cells in the Dominant megacolon mutant, a mouse model of Hirschsprung's disease
    Huang, Taida
    Hou, Yonghui
    Chan, Wood Yee
    FASEB JOURNAL, 2016, 30
  • [25] Differentiation and characterization of PAX6 mutant human embryonic stem cells derived from a family affected with aniridia
    Eason, Jessica
    Smith, Gary
    Bohnsack, Brenda L.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2016, 57 (12)
  • [26] Xenopus pax6 mutants affect eye development and other organ systems, and have phenotypic similarities to human aniridia patients
    Nakayama, Takuya
    Fisher, Marilyn
    Nakajima, Keisuke
    Odeleye, Akinleye O.
    Zimmerman, Keith B.
    Fish, Margaret B.
    Yaoita, Yoshio
    Chojnowski, Jena L.
    Lauderdale, James D.
    Netland, Peter A.
    Grainger, Robert M.
    DEVELOPMENTAL BIOLOGY, 2015, 408 (02) : 328 - 344
  • [27] A new gestational diabetes mellitus model: hyperglycemia-induced eye malformation via inhibition of Pax6 in the chick embryo
    Zhang, Shi-Jie
    Li, Yi-Fang
    Tan, Rui-Rong
    Tsoi, Bun
    Huang, Wen-Shan
    Huang, Yi-Hua
    Tang, Xiao-Long
    Hu, Dan
    Yao, Nan
    Yang, Xuesong
    Kurihara, Hiroshi
    Wang, Qi
    He, Rong-Rong
    DISEASE MODELS & MECHANISMS, 2016, 9 (02) : 177 - 186
  • [28] Non-malignant migration of B16 mouse melanoma cells in the neural crest and invasive growth in the eye cup of the chick embryo
    Oppitz, Matthias
    Busch, Christian
    Schriek, Gernot
    Metzger, Marco
    Just, Lothar
    Drews, Ulrich
    MELANOMA RESEARCH, 2007, 17 (01) : 17 - 30
  • [29] LHX2 regulates the neural differentiation of human embryonic stem cells via transcriptional modulation of PAX6 and CER1
    Hou, Pei-Shan
    Chuang, Ching-Yu
    Kao, Cheng-Fu
    Chou, Shen-Ju
    Stone, Lee
    Ho, Hong-Nerng
    Chien, Chung-Liang
    Kuo, Hung-Chih
    NUCLEIC ACIDS RESEARCH, 2013, 41 (16) : 7753 - 7770
  • [30] In vitro differentiation of adipose-tissue-derived mesenchymal stem cells into neural retinal cells through expression of human PAX6 (5a) gene
    Rezanejad, Habib
    Soheili, Zahra-Soheila
    Haddad, Farhang
    Matin, Maryam M.
    Samiei, Shahram
    Manafi, Ali
    Ahmadieh, Hamid
    CELL AND TISSUE RESEARCH, 2014, 356 (01) : 65 - 75