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OVOL2 Maintains the Transcriptional Program of Human Corneal Epithelium by Suppressing Epithelial-to-Mesenchymal Transition.
Kitazawa, Koji; Hikichi, Takafusa; Nakamura, Takahiro; Mitsunaga, Kanae; Tanaka, Azusa; Nakamura, Masahiro; Yamakawa, Tatsuya; Furukawa, Shiori; Takasaka, Mieko; Goshima, Naoki; Watanabe, Akira; Okita, Keisuke; Kawasaki, Satoshi; Ueno, Morio; Kinoshita, Shigeru; Masui, Shinji.
Afiliação
  • Kitazawa K; Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho Shogoin Sakyo-ku, Kyoto 606-8507, Japan; Department of Ophthalmology, Kyoto Prefectural University of Medicine, 465 Kajii-cho Hirokoji-agaru Kawaramachi-dori Kamigyo-ku, Kyoto 602-0841, Japan; Department of Frontier Medi
  • Hikichi T; Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho Shogoin Sakyo-ku, Kyoto 606-8507, Japan.
  • Nakamura T; Department of Ophthalmology, Kyoto Prefectural University of Medicine, 465 Kajii-cho Hirokoji-agaru Kawaramachi-dori Kamigyo-ku, Kyoto 602-0841, Japan; Department of Frontier Medical Science and Technology for Ophthalmology, Kyoto Prefectural University of Medicine, 465 Kajii-cho Hirokoji-agaru Kawa
  • Mitsunaga K; Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho Shogoin Sakyo-ku, Kyoto 606-8507, Japan.
  • Tanaka A; Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho Shogoin Sakyo-ku, Kyoto 606-8507, Japan.
  • Nakamura M; Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho Shogoin Sakyo-ku, Kyoto 606-8507, Japan.
  • Yamakawa T; Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho Shogoin Sakyo-ku, Kyoto 606-8507, Japan.
  • Furukawa S; Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho Shogoin Sakyo-ku, Kyoto 606-8507, Japan.
  • Takasaka M; JBIC Research Institute, Japan Biological Informatics Consortium, TIME24 Building 10F 2-4-32 Aomi Koto-ku, Tokyo 135-8073, Japan.
  • Goshima N; Molecular Profiling Research Center for Drug Discovery, National Institute of Advanced Industrial Science and Technology, Waterfront Bio-IT Research Building, 2-4-7 Aomi Koto-ku, Tokyo 135-0064, Japan.
  • Watanabe A; Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho Shogoin Sakyo-ku, Kyoto 606-8507, Japan.
  • Okita K; Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho Shogoin Sakyo-ku, Kyoto 606-8507, Japan.
  • Kawasaki S; Department of Ophthalmology, Kyoto Prefectural University of Medicine, 465 Kajii-cho Hirokoji-agaru Kawaramachi-dori Kamigyo-ku, Kyoto 602-0841, Japan; Department of Ophthalmology, Osaka University, 2-2 Yamadaoka Suita, Osaka 565-0871, Japan.
  • Ueno M; Department of Ophthalmology, Kyoto Prefectural University of Medicine, 465 Kajii-cho Hirokoji-agaru Kawaramachi-dori Kamigyo-ku, Kyoto 602-0841, Japan.
  • Kinoshita S; Department of Ophthalmology, Kyoto Prefectural University of Medicine, 465 Kajii-cho Hirokoji-agaru Kawaramachi-dori Kamigyo-ku, Kyoto 602-0841, Japan; Department of Frontier Medical Science and Technology for Ophthalmology, Kyoto Prefectural University of Medicine, 465 Kajii-cho Hirokoji-agaru Kawa
  • Masui S; Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho Shogoin Sakyo-ku, Kyoto 606-8507, Japan; CREST (Core Research for Evolutional Science and Technology), JST (Japan Science and Technology Agency), Honcho 4-1-8 Kawaguchi, Saitama 332-0012, Japan. Electronic address: smasu
Cell Rep ; 15(6): 1359-68, 2016 05 10.
Article em En | MEDLINE | ID: mdl-27134177
ABSTRACT
In development, embryonic ectoderm differentiates into neuroectoderm and surface ectoderm using poorly understood mechanisms. Here, we show that the transcription factor OVOL2 maintains the transcriptional program of human corneal epithelium cells (CECs), a derivative of the surface ectoderm, and that OVOL2 may regulate the differential transcriptional programs of the two lineages. A functional screen identified OVOL2 as a repressor of mesenchymal genes to maintain CECs. Transduction of OVOL2 with several other transcription factors induced the transcriptional program of CECs in fibroblasts. Moreover, neuroectoderm derivatives were found to express mesenchymal genes, and OVOL2 alone could induce the transcriptional program of CECs in neural progenitors by repressing these genes while activating epithelial genes. Our data suggest that the difference between the transcriptional programs of some neuroectoderm- and surface ectoderm-derivative cells may be regulated in part by a reciprocally repressive mechanism between epithelial and mesenchymal genes, as seen in epithelial-to-mesenchymal transition.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Transcrição Gênica / Epitélio Corneano / Transição Epitelial-Mesenquimal Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Cell Rep Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Transcrição Gênica / Epitélio Corneano / Transição Epitelial-Mesenquimal Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Cell Rep Ano de publicação: 2016 Tipo de documento: Article