Evidence map›Paper›PMID 19528298›Full record

ArticleThe Journal of cell biology2009

HUMMR, a hypoxia- and HIF-1alpha-inducible protein, alters mitochondrial distribution and transport.

Yan Li, Seung Lim, David Hoffman, Pontus Aspenstrom, Howard J Federoff, David A Rempe

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
2.4field-weighted citation impact, top 12% of its field
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

53 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
  2. Neurobiology of mitochondrial dynamics in sleep.The Journal of physiology · 2025
    Review
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  18. Mitochondrial transfer from mesenchymal stem cells improves neuronal metabolism after oxidant injury in vitro: The role of Miro1.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  19. Human microsporidian pathogenJournal of cell science · 2021
    Article
  20. Review
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

6 authors at 3 institutions in 2 countries.

Yan LiDepartment of Neurology, Center for Neural Development and Disease, University of Rochester School of Medicine & Dentistry, Rochester, NY 14642, USA.
Seung Lim
David Hoffman
Pontus Aspenstrom
Howard J Federoff
David A Rempe
University of Rochester · USGeorgetown University Medical Center · USKarolinska Institutet · SE

Funding

The Role of Astrocytes in Ischemic StrokeP01NS050315 · NINDS · UNIVERSITY OF ROCHESTER · PI GOLDMAN, STEVEN ALAN · 2007 to 2011
$6.1M
The role of Hypoxia Inducible Factor-1 alpha in strokeK08NS046633 · NINDS · UNIVERSITY OF ROCHESTER · PI REMPE, DAVID · 2003 to 2007
$835k
NINDS NIH HHS 1P01NS050315NINDS NIH HHS K08 NS046633NINDS NIH HHS P01 NS050315
6 · The paper itself

Abstract

Mitochondrial transport is critical for maintenance of normal neuronal function. Here, we identify a novel mitochondria protein, hypoxia up-regulated mitochondrial movement regulator (HUMMR), which is expressed in neurons and is markedly induced by hypoxia-inducible factor 1 alpha (HIF-1alpha). Interestingly, HUMMR interacts with Miro-1 and Miro-2, mitochondrial proteins that are critical for mediating mitochondrial transport. Interestingly, knockdown of HUMMR or HIF-1 function in neurons exposed to hypoxia markedly reduces mitochondrial content in axons. Because mitochondrial transport and distribution are inextricably linked, the impact of reduced HUMMR function on the direction of mitochondrial transport was also explored. Loss of HUMMR function in hypoxia diminished the percentage of motile mitochondria moving in the anterograde direction and enhanced the percentage moving in the retrograde direction. Thus, HUMMR, a novel mitochondrial protein induced by HIF-1 and hypoxia, biases mitochondria transport in the anterograde direction. These findings have broad implications for maintenance of neuronal viability and function during physiological and pathological states.

Indexed as

AnimalsAstrocytesAxonsBase SequenceBiological TransportCarrier ProteinsCells, CulturedCerebral CortexHumansHypoxiaHypoxia-Inducible Factor 1, alpha SubunitIntracellular Signaling Peptides and ProteinsMembrane ProteinsMiceMice, TransgenicMitochondriaCarrier ProteinsFIS1 protein, humanHypoxia-Inducible Factor 1, alpha SubunitIntracellular Signaling Peptides and ProteinsMembrane ProteinsMitochondrial ProteinsMultiprotein ComplexesNerve Tissue Proteinsrho GTP-Binding ProteinsRHOT1 protein, humanRHOT2 protein, humanTRAK2 protein, human

Identifiers

PMID19528298
PMCPMC2711615
OpenAlexW1972665053

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

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.