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Presenilins are enriched in endoplasmic reticulum membranes associated with mitochondria.


ABSTRACT: Presenilin-1 (PS1) and -2 (PS2), which when mutated cause familial Alzheimer disease, have been localized to numerous compartments of the cell, including the endoplasmic reticulum, Golgi, nuclear envelope, endosomes, lysosomes, the plasma membrane, and mitochondria. Using three complementary approaches, subcellular fractionation, gamma-secretase activity assays, and immunocytochemistry, we show that presenilins are highly enriched in a subcompartment of the endoplasmic reticulum that is associated with mitochondria and that forms a physical bridge between the two organelles, called endoplasmic reticulum-mitochondria-associated membranes. A localization of PS1 and PS2 in mitochondria-associated membranes may help reconcile the disparate hypotheses regarding the pathogenesis of Alzheimer disease and may explain many seemingly unrelated features of this devastating neurodegenerative disorder.

SUBMITTER: Area-Gomez E 

PROVIDER: S-EPMC2774047 | biostudies-literature | 2009 Nov

REPOSITORIES: biostudies-literature

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Presenilins are enriched in endoplasmic reticulum membranes associated with mitochondria.

Area-Gomez Estela E   de Groof Ad J C AJ   Boldogh Istvan I   Bird Thomas D TD   Gibson Gary E GE   Koehler Carla M CM   Yu Wai Haung WH   Duff Karen E KE   Yaffe Michael P MP   Pon Liza A LA   Schon Eric A EA  

The American journal of pathology 20091015 5


Presenilin-1 (PS1) and -2 (PS2), which when mutated cause familial Alzheimer disease, have been localized to numerous compartments of the cell, including the endoplasmic reticulum, Golgi, nuclear envelope, endosomes, lysosomes, the plasma membrane, and mitochondria. Using three complementary approaches, subcellular fractionation, gamma-secretase activity assays, and immunocytochemistry, we show that presenilins are highly enriched in a subcompartment of the endoplasmic reticulum that is associat  ...[more]

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