Evidence map›Paper›PMID 11120756›Full record

ArticleThe Journal of clinical investigation2000

Clearance of Alzheimer's amyloid-ss(1-40) peptide from brain by LDL receptor-related protein-1 at the blood-brain barrier.

M Shibata, S Yamada, S R Kumar, M Calero, J Bading, B Frangione, D M Holtzman, C A Miller, D K Strickland, J Ghiso and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 689 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
689citing papers in PubMed, 1 pooled it
13.6field-weighted citation impact, top 1% 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

689 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,373 citations in OpenAlex.

  1. Pooled it
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  9. Glycocalyx and basal lamina in neurological disorders.Matrix biology : journal of the International Society for Matrix Biology · 2026
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629 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

11 authors at 5 institutions in 1 country.

M ShibataDepartment of Neurological Surgery, Keck School of Medicine of the University of Southern California, Los Angeles, California, USA.
S Yamada
S R Kumar
M Calero
J Bading
B Frangione
D M Holtzman
C A Miller
D K Strickland
J Ghiso
B V Zlokovic
University of Southern California · USColumbia University Irving Medical Center · USNeurological Surgery · USAmerican Red Cross · USWashington University in St. Louis · US

Funding

VASCULAR RISK AND COGNITIVE STATUS IN A LATINO POPULATIONP50AG005142 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ARANDA, MARIA P. · 1985 to 2019
$41.0M
CORE--NEUROPATHOLOGYP01AG016223 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZLOKOVIC, BERISLAV V · 1999 to 2003
$4.5M
Regulation of Surface Receptors by LRPR01HL050784 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI STRICKLAND, DUDLEY K. · 1993 to 2011
$3.8M
Effect of apoE on CNS neurons: Role of LRPR37AG013956 · NIA · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M. · 2004 to 2013
$3.8M
AMYLOIDOSIS AND ALZHEIMERS DISEASER37AG005891 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI FRANGIONE, BLAS · 1997 to 2006
$3.3M
ALZHEIMER AMYLOID B AND THE AGED CEREBRAL VESSEL WALLR01NS038777 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GHISO, JORGE A · 2000 to 2004
$1.3M
APOE EFFECT ON CNS NEURONS--ROLE OF LRPR01AG013956 · NIA · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M · 1996 to 2003
$1.2M
AMYLOIDOSIS AND ALZHEIMERS DISEASER01AG005891 · NIA · NEW YORK UNIVERSITY · PI FRANGIONE, BLAS · 1985 to 1995
–
NHLBI NIH HHS R01 HL050784NIA NIH HHS AG05891NIA NIH HHS AG16223NIA NIH HHS P50 AG005142NIA NIH HHS R01 AG013956NIA NIH HHS R37 AG005891NIA NIH HHS R37 AG013956NINDS NIH HHS NS33466NINDS NIH HHS R01 NS038777
6 · The paper itself

Abstract

Elimination of amyloid-ss peptide (Ass) from the brain is poorly understood. After intracerebral microinjections in young mice, (125)I-Ass(1-40) was rapidly removed from the brain (t(1/2) </= 25 minutes), mainly by vascular transport across the blood-brain barrier (BBB). The efflux transport system for Ass(1-40) at the BBB was half saturated at 15.3 nM, and the maximal transport capacity was reached between 70 nM and 100 nM. Ass(1-40) clearance was substantially inhibited by the receptor-associated protein, and by antibodies against LDL receptor-related protein-1 (LRP-1) and alpha(2)-macroglobulin (alpha(2)M). As compared to adult wild-type mice, clearance was significantly reduced in young and old apolipoprotein E (apoE) knockout mice, and in old wild-type mice. There was no evidence that Ass was metabolized in brain interstitial fluid and degraded to smaller peptide fragments and amino acids before its transport across the BBB into the circulation. LRP-1, although abundant in brain microvessels in young mice, was downregulated in older animals, and this downregulation correlated with regional Ass accumulation in brains of Alzheimer's disease (AD) patients. We conclude that the BBB removes Ass from the brain largely via age-dependent, LRP-1-mediated transport that is influenced by alpha(2)M and/or apoE, and may be impaired in AD.

Indexed as

Blood-Brain BarrierAgingalpha-MacroglobulinsAlzheimer DiseaseAmino Acid SequenceAmyloid beta-PeptidesAnimalsApolipoproteins EBiological TransportBrainCatheterizationGenotypeHalf-LifeHumansImmunohistochemistryInulinalpha-MacroglobulinsAmyloid beta-Peptidesamyloid beta-protein (1-40)Apolipoproteins EInulinIodine RadioisotopesLow Density Lipoprotein Receptor-Related Protein-1Peptide FragmentsReceptors, Immunologic

Identifiers

PMID11120756
PMCPMC387254
OpenAlexW1997822484

What OpenQuestion holds

Textmetadata
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.