Literature DB >> 35829808

Cholesterol homeostasis regulated by ABCA1 is critical for retinal ganglion cell survival.

Jialiang Yang1, Yuhong Chen2, Tongdan Zou1, Bai Xue1, Fang Yang1, Xiangzhou Wang3, Yibo Huo3, Boyun Yan3, Yuxia Xu1, Shiyu He1, Yi Yin4, Jing Wang4, Xiong Zhu1, Lin Zhang1, Yu Zhou1, Zhengfu Tai1, Ping Shuai1, Man Yu5, Qian Luo5, Yilian Cheng5, Bo Gong1,6, Xianjun Zhu1,6, Jing Zhang3, Xinghuai Sun2, Ying Lin1, Houbin Zhang7, Zhenglin Yang8,9,10.   

Abstract

Genome-wide association studies have suggested a link between primary open-angle glaucoma and the function of ABCA1. ABCA1 is a key regulator of cholesterol efflux and the biogenesis of high-density lipoprotein (HDL) particles. Here, we showed that the POAG risk allele near ABCA1 attenuated ABCA1 expression in cultured cells. Consistently, POAG patients exhibited lower ABCA1 expression, reduced HDL, and higher cholesterol in white blood cells. Ablation of Abca1 in mice failed to form HDL, leading to elevated cholesterol levels in the retina. Counting retinal ganglion cells (RGCs) by using an artificial intelligence (AI) program revealed that Abca1-deficient mice progressively lost RGCs with age. Single-cell RNA sequencing (scRNA-seq) revealed aberrant oxidative phosphorylation in the Abca1-/- retina, as well as activation of the mTORC1 signaling pathway and suppression of autophagy. Treatment of Abca1-/- mice using atorvastatin reduced the cholesterol level in the retina, thereby improving metabolism and protecting RGCs from death. Collectively, we show that lower ABCA1 expression and lower HDL are risk factors for POAG. Accumulated cholesterol in the Abca1-/- retina causes profound aberrant metabolism, leading to a POAG-like phenotype that can be prevented by atorvastatin. Our findings establish statin use as a preventive treatment for POAG associated with lower ABCA1 expression.
© 2022. Science China Press and Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  ABCA1; HDL; atorvastatin; cholesterol; glaucoma; retinal ganglion cell

Year:  2022        PMID: 35829808     DOI: 10.1007/s11427-021-2126-2

Source DB:  PubMed          Journal:  Sci China Life Sci        ISSN: 1674-7305            Impact factor:   10.372


  40 in total

1.  The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease.

Authors:  M Bodzioch; E Orsó; J Klucken; T Langmann; A Böttcher; W Diederich; W Drobnik; S Barlage; C Büchler; M Porsch-Ozcürümez; W E Kaminski; H W Hahmann; K Oette; G Rothe; C Aslanidis; K J Lackner; G Schmitz
Journal:  Nat Genet       Date:  1999-08       Impact factor: 38.330

2.  Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.

Authors:  A Brooks-Wilson; M Marcil; S M Clee; L H Zhang; K Roomp; M van Dam; L Yu; C Brewer; J A Collins; H O Molhuizen; O Loubser; B F Ouelette; K Fichter; K J Ashbourne-Excoffon; C W Sensen; S Scherer; S Mott; M Denis; D Martindale; J Frohlich; K Morgan; B Koop; S Pimstone; J J Kastelein; J Genest; M R Hayden
Journal:  Nat Genet       Date:  1999-08       Impact factor: 38.330

3.  Lipid and fatty acid profile of the retina, retinal pigment epithelium/choroid, and the lacrimal gland, and associations with adipose tissue fatty acids in human subjects.

Authors:  Lionel Bretillon; Gilles Thuret; Stéphane Grégoire; Niyazi Acar; Corinne Joffre; Alain M Bron; Philippe Gain; Catherine P Creuzot-Garcher
Journal:  Exp Eye Res       Date:  2008-08-29       Impact factor: 3.467

4.  Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma.

Authors:  Yuhong Chen; Ying Lin; Eranga N Vithana; Liyun Jia; Xianbo Zuo; Tien Yin Wong; Li Jia Chen; Xianjun Zhu; Pancy O S Tam; Bo Gong; Shaohong Qian; Zheng Li; Xiaoqi Liu; Baskaran Mani; Qian Luo; Celeste Guzman; Christopher K S Leung; Xiaobo Li; Wenjun Cao; Quanyao Yang; Clement C Y Tham; Yilian Cheng; Xuejun Zhang; Ningli Wang; Tin Aung; Chiea Chuen Khor; Chi Pui Pang; Xinghuai Sun; Zhenglin Yang
Journal:  Nat Genet       Date:  2014-08-31       Impact factor: 38.330

5.  Copy number variations on chromosome 12q14 in patients with normal tension glaucoma.

Authors:  John H Fingert; Alan L Robin; Jennifer L Stone; Ben R Roos; Lea K Davis; Todd E Scheetz; Steve R Bennett; Thomas H Wassink; Young H Kwon; Wallace L M Alward; Robert F Mullins; Val C Sheffield; Edwin M Stone
Journal:  Hum Mol Genet       Date:  2011-03-29       Impact factor: 6.150

6.  Importance of a novel oxidative mechanism for elimination of brain cholesterol. Turnover of cholesterol and 24(S)-hydroxycholesterol in rat brain as measured with 18O2 techniques in vivo and in vitro.

Authors:  I Björkhem; D Lütjohann; O Breuer; A Sakinis; A Wennmalm
Journal:  J Biol Chem       Date:  1997-11-28       Impact factor: 5.157

7.  Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.

Authors:  Kathryn P Burdon; Stuart Macgregor; Alex W Hewitt; Shiwani Sharma; Glyn Chidlow; Richard A Mills; Patrick Danoy; Robert Casson; Ananth C Viswanathan; Jimmy Z Liu; John Landers; Anjali K Henders; John Wood; Emmanuelle Souzeau; April Crawford; Paul Leo; Jie Jin Wang; Elena Rochtchina; Dale R Nyholt; Nicholas G Martin; Grant W Montgomery; Paul Mitchell; Matthew A Brown; David A Mackey; Jamie E Craig
Journal:  Nat Genet       Date:  2011-05-01       Impact factor: 38.330

8.  Lack of Niemann-Pick type C1 induces age-related degeneration in the mouse retina.

Authors:  Thomas Claudepierre; Michel Paques; Manuel Simonutti; Isabelle Buard; Jose Sahel; Robert A Maue; Serge Picaud; Frank W Pfrieger
Journal:  Mol Cell Neurosci       Date:  2009-10-31       Impact factor: 4.314

9.  Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.

Authors:  Jessica N Cooke Bailey; Stephanie J Loomis; Jae H Kang; R Rand Allingham; Puya Gharahkhani; Chiea Chuen Khor; Kathryn P Burdon; Hugues Aschard; Daniel I Chasman; Robert P Igo; Pirro G Hysi; Craig A Glastonbury; Allison Ashley-Koch; Murray Brilliant; Andrew A Brown; Donald L Budenz; Alfonso Buil; Ching-Yu Cheng; Hyon Choi; William G Christen; Gary Curhan; Immaculata De Vivo; John H Fingert; Paul J Foster; Charles Fuchs; Douglas Gaasterland; Terry Gaasterland; Alex W Hewitt; Frank Hu; David J Hunter; Anthony P Khawaja; Richard K Lee; Zheng Li; Paul R Lichter; David A Mackey; Peter McGuffin; Paul Mitchell; Sayoko E Moroi; Shamira A Perera; Keating W Pepper; Qibin Qi; Tony Realini; Julia E Richards; Paul M Ridker; Eric Rimm; Robert Ritch; Marylyn Ritchie; Joel S Schuman; William K Scott; Kuldev Singh; Arthur J Sit; Yeunjoo E Song; Rulla M Tamimi; Fotis Topouzis; Ananth C Viswanathan; Shefali Setia Verma; Douglas Vollrath; Jie Jin Wang; Nicole Weisschuh; Bernd Wissinger; Gadi Wollstein; Tien Y Wong; Brian L Yaspan; Donald J Zack; Kang Zhang; Epic-Norfolk Eye Study; Robert N Weinreb; Margaret A Pericak-Vance; Kerrin Small; Christopher J Hammond; Tin Aung; Yutao Liu; Eranga N Vithana; Stuart MacGregor; Jamie E Craig; Peter Kraft; Gareth Howell; Michael A Hauser; Louis R Pasquale; Jonathan L Haines; Janey L Wiggs
Journal:  Nat Genet       Date:  2016-01-11       Impact factor: 38.330

Review 10.  Optic neuropathies: the tip of the neurodegeneration iceberg.

Authors:  Valerio Carelli; Chiara La Morgia; Fred N Ross-Cisneros; Alfredo A Sadun
Journal:  Hum Mol Genet       Date:  2017-10-01       Impact factor: 6.150

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