Role of retinal pigment epithelium in age-related macular disease: a systematic review

被引:21
作者
Bird, Alan [1 ]
机构
[1] Moorfields Eye Hosp NHS Fdn Trust, Genet, City Rd, London EC1 V2PD, England
关键词
Retina; Vision; Physiology; Genetics; Macula; MITOCHONDRIAL-DNA HAPLOGROUPS; FACTOR-H POLYMORPHISM; FUNDUS AUTOFLUORESCENCE; GEOGRAPHIC ATROPHY; PHOTORECEPTOR DEGENERATION; FATTY-ACID; LIPOFUSCIN; CHOLESTEROL; RPE; ROD;
D O I
10.1136/bjophthalmol-2020-317447
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Age-related macular disease (AMD) is a major cause of blindness and there is little treatment currently available by which the progress of the basic disorder can be modulated. Histological and clinical studies show that the major tissues involved are the outer retina, retinal pigment epithelium, Bruch's membrane and choroid. Because of a wide variation of phenotype from one case to another, it has been suggested that accurate phenotyping would be necessary for assessment of the effectiveness of treatment that is tissue-directed. However, based on findings from the study of human donor material and animal models of disease and of cell culture, it is concluded that retinal pigment epithelial dysfunction plays a central role in the disease process in most, if not all, cases of early AMD. The metabolism of phagosomal material, particularly lipids, and energy generation are interdependent, and dysfunction of both appears to be important in the genesis of disease. Evidence exists to suggest that both can be modulated therapeutically. These metabolic functions are amenable to further investigation in both the normal state and in disease. Once fully characterised, it is likely that treatment could be directed towards a limited number of functions in single tissue, thus simplifying treatment strategies.
引用
收藏
页码:1469 / 1474
页数:6
相关论文
共 95 条
  • [31] Increased retinal mtDNA damage in the CFH variant associated with age-related macular degeneration
    Ferrington, Deborah A.
    Kapphahn, Rebecca J.
    Leary, Michaela M.
    Atilano, Shari R.
    Terluk, Marcia R.
    Karunadharma, Pabalu
    Chen, George Kuei-Jie
    Ratnapriya, Rinki
    Swaroop, Anand
    Montezuma, Sandra R.
    Kenney, M. Cristina
    [J]. EXPERIMENTAL EYE RESEARCH, 2016, 145 : 269 - 277
  • [32] FLANNERY JG, 1990, INVEST OPHTH VIS SCI, V31, P229
  • [33] A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
    Fritsche, Lars G.
    Igl, Wilmar
    Bailey, Jessica N. Cooke
    Grassmann, Felix
    Sengupta, Sebanti
    Bragg-Gresham, Jennifer L.
    Burdon, Kathryn P.
    Hebbring, Scott J.
    Wen, Cindy
    Gorski, Mathias
    Kim, Ivana K.
    Cho, David
    Zack, Donald
    Souied, Eric
    Scholl, Hendrik P. N.
    Bala, Elisa
    Lee, Kristine E.
    Hunter, David J.
    Sardell, Rebecca J.
    Mitchell, Paul
    Merriam, Joanna E.
    Cipriani, Valentina
    Hoffman, Joshua D.
    Schick, Tina
    Lechanteur, Yara T. E.
    Guymer, Robyn H.
    Johnson, Matthew P.
    Jiang, Yingda
    Stanton, Chloe M.
    Buitendijk, Gabrielle H. S.
    Zhan, Xiaowei
    Kwong, Alan M.
    Boleda, Alexis
    Brooks, Matthew
    Gieser, Linn
    Ratnapriya, Rinki
    Branham, Kari E.
    Foerster, Johanna R.
    Heckenlively, John R.
    Othman, Mohammad I.
    Vote, Brendan J.
    Liang, Helena Hai
    Souzeau, Emmanuelle
    McAllister, Ian L.
    Isaacs, Timothy
    Hall, Janette
    Lake, Stewart
    Mackey, David A.
    Constable, Ian J.
    Craig, Jamie E.
    [J]. NATURE GENETICS, 2016, 48 (02) : 134 - 143
  • [34] Dysfunctional autophagy in RPE, a contributing factor in age-related macular degeneration
    Golestaneh, Nady
    Chu, Yi
    Xiao, Yang-Yu
    Stoleru, Gianna L.
    Theos, Alexander C.
    [J]. CELL DEATH & DISEASE, 2017, 8 : e2537 - e2537
  • [35] Lysosomal alkalinization, lipid oxidation, and reduced phagosome clearance triggered by activation of the P2X7 receptor
    Guha, Sonia
    Baltazar, Gabriel C.
    Coffey, Erin E.
    Tu, Leigh-Anne
    Lim, Jason C.
    Beckel, Jonathan M.
    Patel, Shaun
    Eysteinsson, Thor
    Lu, Wennan
    O'Brien-Jenkins, Ann
    Laties, Alan M.
    Mitchell, Claire H.
    [J]. FASEB JOURNAL, 2013, 27 (11) : 4500 - 4509
  • [36] A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration
    Hageman, GS
    Anderson, DH
    Johnson, LV
    Hancox, LS
    Taiber, AJ
    Hardisty, LI
    Hageman, JL
    Stockman, HA
    Borchardt, JD
    Gehrs, KM
    Smith, RJH
    Silvestri, G
    Russell, SR
    Klaver, CCW
    Barbazetto, I
    Chang, S
    Yannuzzi, LA
    Barile, GR
    Merriam, JC
    Smith, RT
    Olsh, AK
    Bergeron, J
    Zernant, J
    Merriam, JE
    Gold, B
    Dean, M
    Allikmets, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (20) : 7227 - 7232
  • [37] The SLC16 gene family - Structure, role and regulation in health and disease
    Halestrap, Andrew P.
    [J]. MOLECULAR ASPECTS OF MEDICINE, 2013, 34 (2-3) : 337 - 349
  • [38] Reduction of lipid accumulation rescues Bietti's crystalline dystrophy phenotypes
    Hata, Masayuki
    Ikeda, Hanako O.
    Iwai, Sachiko
    Iida, Yuto
    Gotoh, Norimoto
    Asaka, Isao
    Ikeda, Kazutaka
    Isobe, Yosuke
    Hori, Aya
    Nakagawa, Saori
    Yamato, Susumu
    Arita, Makoto
    Yoshimura, Nagahisa
    Tsujikawa, Akitaka
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (15) : 3936 - 3941
  • [39] DEGRADATION OF ROD OUTER SEGMENT PROTEINS BY CATHEPSIN-D
    HAYASAKA, S
    HARA, S
    MIZUNO, K
    [J]. JOURNAL OF BIOCHEMISTRY, 1975, 78 (06) : 1365 - 1367
  • [40] HOGAN M J, 1972, Transactions of the American Academy of Ophthalmology and Oto-Laryngology, V76, P64