Evidence map›Paper›PMID 29491385›Full record

ReviewCell death & disease2018

Mitochondria-associated membranes in aging and senescence: structure, function, and dynamics.

Justyna Janikiewicz, Jędrzej Szymański, Dominika Malinska, Paulina Patalas-Krawczyk, Bernadeta Michalska, Jerzy Duszyński, Carlotta Giorgi, Massimo Bonora, Agnieszka Dobrzyn, Mariusz R Wieckowski

Abstract readReview
In one paragraph

Review in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 155 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
155citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

155 citing papers in PubMed, 1 synthesis or guideline pooled it.

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95 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Justyna JanikiewiczDepartment of Biochemistry, Nencki Institute of Experimental Biology, Warsaw, Poland.
Jędrzej SzymańskiDepartment of Biochemistry, Nencki Institute of Experimental Biology, Warsaw, Poland.
Dominika MalinskaDepartment of Biochemistry, Nencki Institute of Experimental Biology, Warsaw, Poland.
Paulina Patalas-KrawczykDepartment of Biochemistry, Nencki Institute of Experimental Biology, Warsaw, Poland.
Bernadeta MichalskaDepartment of Biochemistry, Nencki Institute of Experimental Biology, Warsaw, Poland.
Jerzy DuszyńskiDepartment of Biochemistry, Nencki Institute of Experimental Biology, Warsaw, Poland.
Carlotta GiorgiDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara, Ferrara, Italy.
Massimo BonoraDepartments of Cell Biology and Gottesman Institute for Stem Cell & Regenerative Medicine Research, Albert Einstein College of Medicine, Bronx, NY, USA.
Agnieszka DobrzynDepartment of Biochemistry, Nencki Institute of Experimental Biology, Warsaw, Poland.
Mariusz R WieckowskiDepartment of Biochemistry, Nencki Institute of Experimental Biology, Warsaw, Poland. m.wieckowski@nencki.gov.pl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sites of close contact between mitochondria and the endoplasmic reticulum (ER) are known as mitochondria-associated membranes (MAM) or mitochondria-ER contacts (MERCs), and play an important role in both cell physiology and pathology. A growing body of evidence indicates that changes observed in the molecular composition of MAM and in the number of MERCs predisposes MAM to be considered a dynamic structure. Its involvement in processes such as lipid biosynthesis and trafficking, calcium homeostasis, reactive oxygen species production, and autophagy has been experimentally confirmed. Recently, MAM have also been studied in the context of different pathologies, including Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, type 2 diabetes mellitus and GM1-gangliosidosis. An underappreciated amount of data links MAM with aging or senescence processes. In the present review, we summarize the current knowledge of basic MAM biology, composition and action, and discuss the potential connections supporting the idea that MAM are significant players in longevity.

Indexed as

AgingAnimalsCellular SenescenceEndoplasmic ReticulumHumansMitochondriaMitochondrial Membranes

Identifiers

PMID29491385
PMCPMC5832430

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.