Loss of OPA1 disturbs cellular calcium homeostasis and sensitizes for excitotoxicity-Reference-Cited by-同舟云学术

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Loss of OPA1 disturbs cellular calcium homeostasis and sensitizes for excitotoxicity

Published:2012-11-09 Issue:2 Volume:20 Page:353-365
ISSN:1350-9047
Container-title:Cell Death & Differentiation
language:en
Short-container-title:Cell Death Differ

Author:

Kushnareva Y E,Gerencser A A,Bossy B,Ju W-K,White A D,Waggoner J,Ellisman M H,Perkins G,Bossy-Wetzel E

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology

Link

http://www.nature.com/articles/cdd2012128.pdf

Reference59 articles.

1. Alexander C, Votruba M, Pesch UE, Thiselton DL, Mayer S, Moore A et al. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nat Genet 2000; 26: 211–215.

2. Delettre C, Lenaers G, Griffoin JM, Gigarel N, Lorenzo C, Belenguer P et al. Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy. Nat Genet 2000; 26: 207–210.

3. Lenaers G, Reynier P, Elachouri G, Soukkarieh C, Olichon A, Belenguer P et al. OPA1 functions in mitochondria and dysfunctions in optic nerve. Int J Biochem Cell Biol 2009; 41: 1866–1874.

4. Ju WK, Misaka T, Kushnareva Y, Nakagomi S, Agarwal N, Kubo Y et al. OPA1 expression in the normal rat retina and optic nerve. J Comp Neurol 2005; 488: 1–10.

5. Pesch UE, Fries JE, Bette S, Kalbacher H, Wissinger B, Alexander C et al. OPA1, the disease gene for autosomal dominant optic atrophy, is specifically expressed in ganglion cells and intrinsic neurons of the retina. Invest Ophthalmol Vis Sci 2004; 45: 4217–4225.

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