Data from: Neuronal migration depends on blood flow in the adult mammalian brain
Data files
Oct 27, 2025 version files 69.43 KB
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Figure_5.csv
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Figure1-figure_supplement_1.csv
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Figure1-figure_supplement_2C.csv
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Figure1-figure_supplement_2E-G.csv
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Figure1-figure_supplement_2H.csv
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Figure1-figure_supplement_3.csv
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Figure1D.csv
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Figure1G.csv
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Figure1H.csv
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Figure1I.csv
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Figure1J.csv
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Figure1K.csv
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Figure1N.csv
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Figure1P.csv
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Figure2-figure_supplement_1.csv
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Figure2C.csv
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Figure2G__H.csv
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Figure3-figure_supplement_1.csv
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Figure3D.csv
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Figure3F.csv
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Figure4B.csv
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Figure4D-J.csv
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Figure4L__M.csv
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Figure5-figure_supplement_1.csv
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Figure5-figure_supplement_2.csv
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Figure5-figure_supplement_3B.csv
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Figure5-figure_supplement_3C.csv
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Figure5-figure_supplement_4.csv
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p_value.csv
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README.md
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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 brain. Neuronal migration is facilitated by blood flow, leading to the 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 the 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 improve the olfactory function for food-seeking behavior during starvation.
Dataset DOI: 10.5061/dryad.dncjsxmcb
Description of the data and file structure
We performed in vitro and in vivo experiments by immunohistochemistry and fluorescent live imaging.
Files and variables
File: p_value.csv
Description: p-value from all data
File: Figure5-figure_supplement_4.csv
Description: Proportion of NeuN+/Dcx- cells among total BrdU+ cells in the OB in the ad libitum (AL) and 70% calorie restriction (CR) groups
File: Figure5-figure_supplement_3B.csv
Description: Proportion of Ghsr1a-KD cells in the OB in the Sham and bilateral carotid artery stenosis (BCAS) groups analyzed by immunohistochemistry in 6 to 12-week-old adult mice
File: Figure5-figure_supplement_2.csv
Description: Quantification of Ki67+ cells in the control/ghsr1a-KD groups in vivo
File: Figure5-figure_supplement_1.csv
Description: Analysis of migration speed in control/ghsr1a-KD new neurons in vivo
File: Figure5-figure_supplement_3C.csv
Description: Normalized density of Control/Ghsr1a-KD in perivascular regions of endomucin-positive/-negative vessels in the RMS in the Sham and bilateral carotid artery stenosis (BCAS) groups analyzed by immunohistochemistry in 6 to 12-week-old adult mice
File: Figure3-figure_supplement_1.csv
Description: Quantification of Ghsr1a mRNA puncta per Dcx+ cell in the OB of the AL and CR mice
File: Figure2-figure_supplement_1.csv
Description: Analysis of the effect of bilateral carotid artery stenosis groups (BCAS) on cell proliferation and survival in the RMS and VSVZ, analyzed by immunohistochemistry in 6 to 12-week-old adult mice
File: Figure1-figure_supplement_2H.csv
Description: Density of BrdU+/Dcx+ cells in the vicinity of endomucin-positive and endomucin-negative vessels in the GL, GCL, and RMS was analyzed by immunohistochemistry in 6 to 12-week-old adult mice
File: Figure1-figure_supplement_3.csv
Description: Density of immature neurons in the vicinity of SLC16A1-positive and -negative vessels in the mice and common marmosets brain
File: Figure_5.csv
Description: Analysis of migration speed in control/ghsr1a-KD new neurons in vivo
File: Figure4D-J.csv
Description: Analysis of migration speed, percentage of migratory phase, migration cycle, length/speed of leading process extension, and stride/speed of somal translocation in neuronal migration in vitro
File: Figure1-figure_supplement_2E-G.csv
Description: Density of BrdU+/Dcx+ cells in the vicinity of endomucin-positive and endomucin-negative vessels in the GL, GCL, and RMS was analyzed by immunohistochemistry in 6 to 12-week-old adult mice
File: Figure1-figure_supplement_2C.csv
Description: Average RBC flow in endomucin-positive and endomucin-negative vessels analyzed by two-photon imaging and immunohistochemistry in 6 to 12-week-old adult mice
File: Figure3D.csv
Description: Normalized fluorescence signal intensity in vascular endothelial cells analyzed by immunohistochemistry in 6 to 12-week-old adult mice
File: Figure4B.csv
Description: Analysis for examining the effect of ghrelin on neuronal migration in vitro
File: Figure1P.csv
Description: Density of newly added neurons in the perivascular region analyzed by two-photon imaging in 6 to 12-week-old adult VGAT-Venus mice, in which GABAergic neurons are labeled with Venus
File: Figure2G__H.csv
Description: Comparison of migration speed before and after laser irradiation in the control (G) and photothrombosis groups (H), analyzed by two-photon imaging in 6 to 12-week-old adult Dcx-EGFP mice
File: Figure3F.csv
Description: Comparison of signal gradient in extra-vessel regions analyzed by immunohistochemistry in 6 to 12-week-old adult mice
File: Figure1N.csv
Description: Density of BrdU+/Dcx+ cells in the perivascular region of arteriole-side and venule-side capillaries analyzed by immunohistchemistry in NG2-DsRed mice
File: Figure1K.csv
Description: Maximum migration speed of new neurons analyzed by two-photon imaging in 6 to 12-week-old adult mice
File: Figure1-figure_supplement_1.csv
Description: Classification of neuron-vessel interaction analyzed by two-photon imaging in 6 to 12-week-old adult Dcx-EGFP mice
File: Figure1J.csv
Description: Percentage of migratory period analyzed by two-photon imaging in 6 to 12-week-old adult mice
File: Figure1I.csv
Description: Average migration speed analyzed by two-photon imaging in 6 to 12-week-old adult mice
File: Figure1H.csv
Description: Density of perivascular migrating cells analyzed by two-photon imaging in 6 to 12-week-old adult mice
File: Figure4L__M.csv
Description: Analysis of the duration of actin cups and migration distance during actin cup formation in new neurons in vitro
File: Figure1D.csv
Description: Distance between new neurons and nearest vessels in the olfactory bulb and RMS analyzed by three-dimensional imaging in 6 to 12-week-old adult mice
File: Figure1G.csv
Description: Average distance between migrating cells and nearest blood vessels analyzed by two-photon imaging in 6 to 12-week-old adult mice
File: Figure2C.csv
Description: Proportion of lentivirally-labeled cells in the OB in the Sham and bilateral carotid artery stenosis groups analyzed by immunohistochemistry in 6 to 12-week-old adult mice
