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Downregulation of AANAT by c-Fos in tubular epithelial cells with membranous nephropathy.
Huang, Yen-Sung; Lo, Chang-Han; Tsai, Ping-Huang; Hou, Yi-Chou; Chang, Yu-Tien; Guo, Cheng-Yi; Hsieh, Hsin-Yi; Lu, Kuo-Cheng; Shih, Hsiu-Ming; Wu, Chia-Chao.
Afiliación
  • Huang YS; Institute of Biomedical Sciences, Academia Sinica, Taipei, 11529, Taiwan. Electronic address: yshuang@ibms.sinica.edu.tw.
  • Lo CH; Division of Nephrology, Department of Internal Medicine, Tri-Service General Hospital Penghu Branch, National Defense Medical Center, Penghu County, 88056, Taiwan; Division of Nephrology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 11490, T
  • Tsai PH; Division of Nephrology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 11490, Taiwan. Electronic address: tsaipinghuang@gmail.com.
  • Hou YC; Division of Nephrology, Department of Medicine, Cardinal-Tien Hospital, School of Medicine, Fu-Jen Catholic University, New Taipei City, 24205, Taiwan. Electronic address: athletics910@gmail.com.
  • Chang YT; School of Public Health, National Defense Medical Center, Taipei, 11490, Taiwan. Electronic address: greengarden720925@gmail.com.
  • Guo CY; Division of Nephrology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 11490, Taiwan. Electronic address: jour90301@yahoo.com.tw.
  • Hsieh HY; Division of Nephrology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 11490, Taiwan. Electronic address: kaki6911@mail.ndmctsgh.edu.tw.
  • Lu KC; Division of Nephrology, Department of Medicine, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City, 23142, Taiwan. Electronic address: kuochenglu@gmail.com.
  • Shih HM; Institute of Biomedical Sciences, Academia Sinica, Taipei, 11529, Taiwan. Electronic address: hmshih@ibms.sinica.edu.tw.
  • Wu CC; Division of Nephrology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, 11490, Taiwan; Department and Graduate Institute of Microbiology and Immunology, National Defense Medical Center, Taipei, 11490, Taiwan. Electronic address: wucc@mail.ndmct
Biochem Biophys Res Commun ; 584: 32-38, 2021 12 20.
Article en En | MEDLINE | ID: mdl-34763165
Melatonin is a hormone majorly secreted by the pineal gland and contributes to a various type of physiological functions in mammals. The melatonin production is tightly limited to the AANAT level, yet the most known molecular mechanisms underlying AANAT gene transcription is limited in the pinealocyte. Here, we find that c-Fos and cAMP-response element-binding protein (CREB) decreases and increases the AANAT transcriptional activity in renal tubular epithelial cell, respectively. Notably, c-Fos knockdown significantly upregulates melatonin levels in renal tubular cells. Functional results indicate that AANAT expression is decreased by c-Fos and resulted in enhancement of cell damage in albumin-injury cell model. We further find an inverse correlation between c-Fos and AANAT levels in renal tubular cells from experimental membranous nephropathy (MN) samples and clinical MN specimens. Our finding provides the molecular basis of c-Fos in transcriptionally downregulating expression of AANAT and melatonin, and elucidate the protective role of AANAT in preventing renal tubular cells death in albumin-injury cell model and MN progression.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glomerulonefritis Membranosa / Regulación hacia Abajo / Proteínas Proto-Oncogénicas c-fos / N-Acetiltransferasa de Arilalquilamina / Células Epiteliales Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Biochem Biophys Res Commun Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glomerulonefritis Membranosa / Regulación hacia Abajo / Proteínas Proto-Oncogénicas c-fos / N-Acetiltransferasa de Arilalquilamina / Células Epiteliales Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Biochem Biophys Res Commun Año: 2021 Tipo del documento: Article