Literature DB >> 27117871

Endoplasmic reticulum stress in human photoreceptor diseases.

Priscilla Chan1, Julia Stolz2, Susanne Kohl2, Wei-Chieh Chiang1, Jonathan H Lin3.   

Abstract

Photoreceptors are specialized sensory neurons essential for light detection in the human eye. Photoreceptor cell dysfunction and death cause vision loss in many eye diseases such as retinitis pigmentosa and achromatopsia. Endoplasmic reticulum (ER) stress and Unfolded Protein Response (UPR) signaling have been implicated in the development and pathology of heritable forms of retinitis pigmentosa and achromatopsia. We review the role of ER stress and UPR in retinitis pigmentosa arising from misfolded rhodopsins (RHO) and in achromatopsia arising from genetic mutations in Activating Transcription Factor 6 (ATF6). This article is part of a Special Issue entitled SI:ER stress. Published by Elsevier B.V.

Entities:  

Keywords:  ATF6; Achromatopsia; Photoreceptor; Retina; Retinitis pigmentosa; Rhodopsin

Mesh:

Substances:

Year:  2016        PMID: 27117871      PMCID: PMC5036988          DOI: 10.1016/j.brainres.2016.04.021

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  41 in total

1.  IRE1 signaling affects cell fate during the unfolded protein response.

Authors:  Jonathan H Lin; Han Li; Douglas Yasumura; Hannah R Cohen; Chao Zhang; Barbara Panning; Kevan M Shokat; Matthew M Lavail; Peter Walter
Journal:  Science       Date:  2007-11-09       Impact factor: 47.728

2.  Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa.

Authors:  C H Sung; B G Schneider; N Agarwal; D S Papermaster; J Nathans
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

3.  A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene.

Authors:  Bo Chang; Tanja Grau; Susann Dangel; Ron Hurd; Bernhard Jurklies; E Cumhur Sener; Sten Andreasson; Helene Dollfus; Britta Baumann; Sylvia Bolz; Nikolai Artemyev; Susanne Kohl; John Heckenlively; Bernd Wissinger
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-03       Impact factor: 11.205

4.  A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.

Authors:  T P Dryja; T L McGee; E Reichel; L B Hahn; G S Cowley; D W Yandell; M A Sandberg; E L Berson
Journal:  Nature       Date:  1990-01-25       Impact factor: 49.962

5.  ATF6alpha optimizes long-term endoplasmic reticulum function to protect cells from chronic stress.

Authors:  Jun Wu; D Thomas Rutkowski; Meghan Dubois; Jayanth Swathirajan; Thomas Saunders; Junying Wang; Benbo Song; Grace D-Y Yau; Randal J Kaufman
Journal:  Dev Cell       Date:  2007-09       Impact factor: 12.270

6.  A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia.

Authors:  Susanne Kohl; Frauke Coppieters; Françoise Meire; Simone Schaich; Susanne Roosing; Christina Brennenstuhl; Sylvia Bolz; Maria M van Genderen; Frans C C Riemslag; Robert Lukowski; Anneke I den Hollander; Frans P M Cremers; Elfride De Baere; Carel B Hoyng; Bernd Wissinger
Journal:  Am J Hum Genet       Date:  2012-08-16       Impact factor: 11.025

7.  XBP-1 regulates a subset of endoplasmic reticulum resident chaperone genes in the unfolded protein response.

Authors:  Ann-Hwee Lee; Neal N Iwakoshi; Laurie H Glimcher
Journal:  Mol Cell Biol       Date:  2003-11       Impact factor: 4.272

8.  Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.

Authors:  Alberta A H J Thiadens; Anneke I den Hollander; Susanne Roosing; Sander B Nabuurs; Renate C Zekveld-Vroon; Rob W J Collin; Elfride De Baere; Robert K Koenekoop; Mary J van Schooneveld; Tim M Strom; Janneke J C van Lith-Verhoeven; Andrew J Lotery; Norka van Moll-Ramirez; Bart P Leroy; L Ingeborgh van den Born; Carel B Hoyng; Frans P M Cremers; Caroline C W Klaver
Journal:  Am J Hum Genet       Date:  2009-07-16       Impact factor: 11.025

9.  Endoplasmic reticulum stress in vertebrate mutant rhodopsin models of retinal degeneration.

Authors:  Heike Kroeger; Matthew M LaVail; Jonathan H Lin
Journal:  Adv Exp Med Biol       Date:  2014       Impact factor: 2.622

10.  The cellular fate of mutant rhodopsin: quality control, degradation and aggresome formation.

Authors:  Richard S Saliba; Peter M G Munro; Philip J Luthert; Michael E Cheetham
Journal:  J Cell Sci       Date:  2002-07-15       Impact factor: 5.285

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  22 in total

Review 1.  Structural and molecular bases of rod photoreceptor morphogenesis and disease.

Authors:  Theodore G Wensel; Zhixian Zhang; Ivan A Anastassov; Jared C Gilliam; Feng He; Michael F Schmid; Michael A Robichaux
Journal:  Prog Retin Eye Res       Date:  2016-06-22       Impact factor: 21.198

Review 2.  ER stress and unfolded protein response in ocular health and disease.

Authors:  Heike Kroeger; Wei-Chieh Chiang; Julia Felden; Amanda Nguyen; Jonathan H Lin
Journal:  FEBS J       Date:  2018-06-20       Impact factor: 5.542

3.  Autosomal recessive cone-rod dystrophy can be caused by mutations in the ATF6 gene.

Authors:  Anna Skorczyk-Werner; Wei-Chieh Chiang; Anna Wawrocka; Katarzyna Wicher; Małgorzata Jarmuż-Szymczak; Magdalena Kostrzewska-Poczekaj; Aleksander Jamsheer; Rafał Płoski; Małgorzata Rydzanicz; Dorota Pojda-Wilczek; Nicole Weisschuh; Bernd Wissinger; Susanne Kohl; Jonathan H Lin; Maciej R Krawczyński
Journal:  Eur J Hum Genet       Date:  2017-08-16       Impact factor: 4.246

Review 4.  Mitigating the pro-oxidant state and melanogenesis of Retinitis pigmentosa: by counteracting mitochondrial dysfunction.

Authors:  Giovanni Pagano; Federico V Pallardó; Alex Lyakhovich; Luca Tiano; Marco Trifuoggi
Journal:  Cell Mol Life Sci       Date:  2021-10-31       Impact factor: 9.261

Review 5.  Gene Therapy Strategies to Restore ER Proteostasis in Disease.

Authors:  Vicente Valenzuela; Kasey L Jackson; Sergio P Sardi; Claudio Hetz
Journal:  Mol Ther       Date:  2018-04-07       Impact factor: 11.454

6.  Gene Therapy Rescues Retinal Degeneration in Receptor Expression-Enhancing Protein 6 Mutant Mice.

Authors:  Smriti Agrawal Zaneveld; Aiden Eblimit; Qingnan Liang; Renae Bertrand; Nathaniel Wu; Hehe Liu; Quynh Nguyen; Jacques Zaneveld; Keqing Wang; Yumei Li; Rui Chen
Journal:  Hum Gene Ther       Date:  2018-10-16       Impact factor: 5.695

7.  REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking.

Authors:  Smriti A Agrawal; Thomas Burgoyne; Aiden Eblimit; James Bellingham; David A Parfitt; Amelia Lane; Ralph Nichols; Chinwe Asomugha; Matthew J Hayes; Peter M Munro; Mingchu Xu; Keqing Wang; Clare E Futter; Yumei Li; Rui Chen; Michael E Cheetham
Journal:  Hum Mol Genet       Date:  2017-07-15       Impact factor: 6.150

Review 8.  Recent Insights into the Role of Unfolded Protein Response in ER Stress in Health and Disease.

Authors:  Dan Lindholm; Laura Korhonen; Ove Eriksson; Sulev Kõks
Journal:  Front Cell Dev Biol       Date:  2017-05-10

9.  Material-driven fibronectin assembly rescues matrix defects due to mutations in collagen IV in fibroblasts.

Authors:  Elie Ngandu Mpoyi; Marco Cantini; Yuan Yan Sin; Lauren Fleming; Dennis W Zhou; Mercedes Costell; Yinhui Lu; Karl Kadler; Andrés J García; Tom Van Agtmael; Manuel Salmeron-Sanchez
Journal:  Biomaterials       Date:  2020-05-03       Impact factor: 12.479

10.  Neuroprotection by eIF2α-CHOP inhibition and XBP-1 activation in EAE/optic neuritiss.

Authors:  Haoliang Huang; Linqing Miao; Feisi Liang; Xiaodong Liu; Lin Xu; Xiuyin Teng; Qizhao Wang; William H Ridder; Kenneth S Shindler; Yang Sun; Yang Hu
Journal:  Cell Death Dis       Date:  2017-07-20       Impact factor: 8.469

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