Evidence map›Paper›PMID 41146614›Full record

ArticleeLife2025

Neuronal migration depends on blood flow in the adult mammalian brain.

Takashi Ogino, Akari Saito, Masato Sawada, Shoko Takemura, Yuzuki Hara, Kanami Yoshimura, Jiro Nagase, Honomi Kawase, Takamasa Sato, Hiroyuki Inada and 6 more

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Takashi Ogino *Department of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0000-0003-1619-8659
Akari Saito *Department of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Masato SawadaDepartment of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Shoko TakemuraDepartment of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0000-0003-1872-4050
Yuzuki HaraDepartment of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Kanami YoshimuraDepartment of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Jiro NagaseDepartment of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Honomi KawaseDepartment of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Takamasa SatoDepartment of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Hiroyuki InadaDivision of Homeostatic Development, Department of Developmental Physiology, National Institute for Physiological Sciences, Okazaki, Japan.
Vicente Herranz-PérezLaboratory of Comparative Neurobiology, Cavanilles Institute, University of Valencia, Valencia, Spain.ORCID https://orcid.org/0000-0002-1969-1214
Yoh-Suke MukouyamaLaboratory of Stem Cell and Neuro-Vascular Biology, Genetics and Developmental Biology Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, United States.
Masatsugu EmaDepartment of Stem Cells and Human Disease Models, Research Center for Animal Life Science, Shiga University of Medical Science, Otsu, Japan.ORCID https://orcid.org/0000-0002-6549-2611
José Manuel García-VerdugoLaboratory of Comparative Neurobiology, Cavanilles Institute, University of Valencia, Valencia, Spain.
Junichi NabekuraDepartment of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0000-0001-5834-6272
Kazunobu SawamotoDepartment of Developmental and Regenerative Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0000-0003-1984-5129

Funding

Japan Agency for Medical Research and Development 24gm1210007Japan Agency for Medical Research and Development 25ym0126807Japan Society for the Promotion of Science 17H05750Japan Society for the Promotion of Science 18KK0213Japan Society for the Promotion of Science 19H04757Japan Society for the Promotion of Science 20H05700Japan Society for the Promotion of Science 22122004Japan Society for the Promotion of Science 23H04939Japan Society for the Promotion of Science 24H02016Japan Society for the Promotion of Science 24K22003Japan Society for the Promotion of Science 25H01040Japan Society for the Promotion of Science 25H02507Japan Society for the Promotion of Science 26640046Japan Society for the Promotion of Science JP22H04926Japan Society for the Promotion of Science JPJSCCA20230007Ministry of Education, Culture, Sports, Science and Technology JPMXS0441500024Nagoya City University 2401101Nagoya City University 2412145National Institute for Physiological Sciences 22NIPS217Spanish Ministry of Science, Innovation and Universities PCI2018-093062
6 · The paper itself

Abstract

In animal tissues, several cell types migrate along blood vessels, raising the possibility that blood flow influences cell migration. Here, we show that blood flow promotes the migration of new olfactory-bulb neurons in the adult mammalian brain. Neuronal migration is facilitated by blood flow, leading to accumulation of new neurons near blood vessels with abundant blood flow. Blood flow inhibition attenuates blood vessel-guided neuronal migration, suggesting that blood contains factors beneficial to neuronal migration. We found that ghrelin, which is increased in blood by hunger, directly influences neuronal migration. Ghrelin signaling promotes somal translocation by activating actin cytoskeleton contraction at the rear of the cell soma. New neurons mature in the olfactory bulb and contribute to the olfactory function for sensing odorants from food. Finally, we show that neuronal migration is increased by calorie restriction, and that ghrelin signaling is involved in the process. This study suggests that blood flow promotes neuronal migration through blood-derived ghrelin signaling in the adult brain, which could be one of the mechanisms that improves the olfactory function for food-seeking behavior during starvation.

Indexed as

BrainCell MovementNeuronsOlfactory BulbAnimalsGhrelinMaleMiceMice, Inbred C57BLSignal TransductionGhrelinadult neurogenesisblood flowcommon marmosetghrelinmouseneuronal migrationneuroscienceolfactory bulbrostral migratory streamventricular-subventricular zone

Identifiers

PMID41146614
PMCPMC12563554

What OpenQuestion holds

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Registered trials

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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.