4.5 Review

The transcription factor MITF in RPE function and dysfunction

Journal

PROGRESS IN RETINAL AND EYE RESEARCH
Volume 73, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.preteyeres.2019.06.002

Keywords

Microphthahnia; Retinal pigment epithelium; Retinal degeneration; Melanocyte

Categories

Funding

  1. National Natural Science Foundation of China [81870664, 81600748, 81570892, 81770946, 81800838]
  2. National Basic Research Program (973 Program) [2009CB526502]
  3. Natural Science Foundation of Zhejiang Province [LY18H120007]
  4. Research Grant of Wenzhou Medical University [QTJ08006]
  5. Wenzhou Medical University Eye Hospital [KYQD151211, YNZD201605, YNCX3201902]
  6. Project of State Key Laboratory of Ophthalmology, Optometry and Visual Science, Wenzhou Medical University [437201804G]
  7. National Institutes of Health, United States

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Dysfunction and loss of the retinal pigment epithelium (RPE) are hallmarks of retinal degenerative diseases in mammals. A critical transcription factor for RPE development and function is the microphthalmia-associated transcription factor MITF and its germline mutations are associated with clinically distinct disorders, including albinism, microphthalmia, retinal degeneration, and increased risk of developing melanoma. Many studies have revealed new insights into central roles of MITF in RPE cell physiology, including melanogenesis, regulation of trophic factor expression, cell proliferation, anti-oxidant functions, and the visual cycle. In this review, we discuss the complex functional roles of MITF in RPE development, homeostasis, and retinal degeneration and touch upon key questions and challenges in neuroprotective strategies for retinal degenerative disorders associated with deficiencies in MITF or its many target genes.

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