Evidence map›Paper›PMID 37102631›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Elevated PDGF-BB from Bone Impairs Hippocampal Vasculature by Inducing PDGFRβ Shedding from Pericytes.

Guanqiao Liu, Jiekang Wang, Zhiliang Wei, Ching-Lien Fang, Ke Shen, Cheng Qian, Cheng Qi, Tong Li, Peisong Gao, Philip C Wong and 3 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 35 citations in OpenAlex.

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  13. Microvascular Health as a Key Determinant of Organismal Aging.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
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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

13 authors at 1 institution in 1 country.

Guanqiao LiuDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Ross Building, Room 232, 720 Rutland Avenue, Baltimore, MD, 21205, USA.
Jiekang WangDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Ross Building, Room 232, 720 Rutland Avenue, Baltimore, MD, 21205, USA.
Zhiliang WeiThe Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Ching-Lien FangDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Ross Building, Room 232, 720 Rutland Avenue, Baltimore, MD, 21205, USA.
Ke ShenDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Ross Building, Room 232, 720 Rutland Avenue, Baltimore, MD, 21205, USA.
Cheng QianDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Ross Building, Room 232, 720 Rutland Avenue, Baltimore, MD, 21205, USA.
Cheng QiDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Ross Building, Room 232, 720 Rutland Avenue, Baltimore, MD, 21205, USA.
Tong LiDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Peisong GaoDivision of Allergy and Clinical Immunology, Johns Hopkins University School of Medicine, Baltimore, MD, 21224, USA.
Philip C WongDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Hanzhang LuThe Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Xu CaoDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Ross Building, Room 232, 720 Rutland Avenue, Baltimore, MD, 21205, USA.
Mei WanDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Ross Building, Room 232, 720 Rutland Avenue, Baltimore, MD, 21205, USA.ORCID 0000-0001-9404-540X
Johns Hopkins University · US

Funding

Skeleton and Joint Degeneration with AgingP01AG066603 · NIA · JOHNS HOPKINS UNIVERSITY · PI CAO, XU · 2021 to 2025
$9.2M
Identifying A Skeleton-Derived Factor for Vascular AgingR01AG072090 · NIA · JOHNS HOPKINS UNIVERSITY · PI WAN, MEI · 2021 to 2025
$2.4M
Role of Cellular Senescence in the Bone-Brain InterplayR01AG068226 · NIA · JOHNS HOPKINS UNIVERSITY · PI WAN, MEI · 2020 to 2024
$2.0M
Subchondral Bone Cavities in Osteoarthritis PainR01AG068997 · NIA · JOHNS HOPKINS UNIVERSITY · PI CAO, XU, GUAN, YUN · 2024 to 2024
$621k
Zeiss LSM780 Confocal Microscope for a Core FacilityS10OD016374 · OD · JOHNS HOPKINS UNIVERSITY · PI KUO, SCOT CHARLES · 2013 to 2013
$584k
NIA NIH HHS P01 AG066603NIA NIH HHS R01 AG068226NIA NIH HHS R01 AG068997NIA NIH HHS R01 AG072090NIH HHS P01AG066603NIH HHS R01 AG068226NIH HHS R01AG072090NIH HHS S10 OD016374
6 · The paper itself

Abstract

Evidence suggests a unique association between bone aging and neurodegenerative/cerebrovascular disorders. However, the mechanisms underlying bone-brain interplay remain elusive. Here platelet-derived growth factor-BB (PDGF-BB) produced by preosteoclasts in bone is reported to promote age-associated hippocampal vascular impairment. Aberrantly elevated circulating PDGF-BB in aged mice and high-fat diet (HFD)-challenged mice correlates with capillary reduction, pericyte loss, and increased blood-brain barrier (BBB) permeability in their hippocampus. Preosteoclast-specific Pdgfb transgenic mice with markedly high plasma PDGF-BB concentration faithfully recapitulate the age-associated hippocampal BBB impairment and cognitive decline. Conversely, preosteoclast-specific Pdgfb knockout mice have attenuated hippocampal BBB impairment in aged mice or HFD-challenged mice. Persistent exposure of brain pericytes to high concentrations of PDGF-BB upregulates matrix metalloproteinase 14 (MMP14), which promotes ectodomain shedding of PDGF receptor β (PDGFRβ) from pericyte surface. MMP inhibitor treatment alleviates hippocampal pericyte loss and capillary reduction in the conditional Pdgfb transgenic mice and antagonizes BBB leakage in aged mice. The findings establish the role of bone-derived PDGF-BB in mediating hippocampal BBB disruption and identify the ligand-induced PDGFRβ shedding as a feedback mechanism for age-associated PDGFRβ downregulation and the consequent pericyte loss.

Indexed as

HippocampusPericytesAnimalsBecaplerminLymphokinesMiceMice, KnockoutMice, TransgenicPlatelet-Derived Growth FactorProto-Oncogene Proteins c-sisReceptor, Platelet-Derived Growth Factor betaBecaplerminLymphokinesPdgfd protein, mousePlatelet-Derived Growth FactorProto-Oncogene Proteins c-sisReceptor, Platelet-Derived Growth Factor betablood-brain barrier permeabilitybonecirculating platelet-derived growth factor-BBPDGFRβreceptor shedding

Identifiers

PMID37102631
PMCPMC10369301
OpenAlexW4367174702

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.