Evidence map›Paper›PMID 30670660›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

A ligand motif enables differential vascular targeting of endothelial junctions between brain and retina.

Fenny H F Tang, Fernanda I Staquicini, André A R Teixeira, Jussara S Michaloski, Gislene M Namiyama, Noemi N Taniwaki, João C Setubal, Aline M da Silva, Richard L Sidman, Renata Pasqualini and 2 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  14. The in vivo endothelial cell translatome is highly heterogeneous across vascular beds.Proceedings of the National Academy of Sciences of the United States of America · 2019
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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

12 authors at 4 institutions in 2 countries.

Fenny H F TangDepartment of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo, SP 05508-000, Brazil.
Fernanda I StaquiciniRutgers Cancer Institute of New Jersey, Newark, NJ 07103.
André A R TeixeiraDepartment of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo, SP 05508-000, Brazil.
Jussara S MichaloskiDepartment of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo, SP 05508-000, Brazil.
Gislene M NamiyamaElectron Microscopy Laboratory, Institute Adolfo Lutz, São Paulo, SP 01246-000, Brazil.
Noemi N TaniwakiElectron Microscopy Laboratory, Institute Adolfo Lutz, São Paulo, SP 01246-000, Brazil.
João C SetubalDepartment of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo, SP 05508-000, Brazil.
Aline M da SilvaDepartment of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo, SP 05508-000, Brazil.
Richard L SidmanDepartment of Neurology, Harvard Medical School, Boston, MA 02115; richard_sidman@hms.harvard.edu giordano@iq.usp.br.
Renata PasqualiniRutgers Cancer Institute of New Jersey, Newark, NJ 07103.
Wadih ArapRutgers Cancer Institute of New Jersey, Newark, NJ 07103.
Ricardo J GiordanoDepartment of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo, SP 05508-000, Brazil; richard_sidman@hms.harvard.edu giordano@iq.usp.br.ORCID 0000-0001-8116-6771
Universidade de São Paulo · BRRutgers, The State University of New Jersey · USInstituto Adolfo Lutz · BRHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelial heterogeneity has important implications in health and disease. Molecular markers selectively expressed in the vasculature of different organs and tissues are currently being explored in targeted therapies with promising results in preclinical and clinical studies. Noteworthy is the role that combinatorial approaches such as phage display have had in identifying such markers by using phage as nanoparticles and surrogates for billions of different peptides, screening noninvasively the vascular lumen for binding sites. Here, we show that a new peptide motif that emerged from such combinatorial screening of the vasculature binds selectively to blood vessels in the brain in vivo but not to vessels in other organs. Peptides containing a conserved motif in which amino acids Phenylalanine-Arginine-Tryptophan (FRW) predominate could be visualized by transmission electron microscopy bound to the junctions between endothelial cells in all areas of the brain, including the optic nerve, but not in other barrier-containing tissues, such as intestines and testis. Remarkably, peptides containing the motif do not bind to vessels in the retina, implying an important molecular difference between these two vascular barriers. Furthermore, the peptide allows for in vivo imaging, demonstrating that new tools for studying and imaging the brain are likely to emerge from this motif.

Indexed as

Amino Acid MotifsLigandsAmino Acid SequenceAnimalsBrainCell Surface Display TechniquesCerebrovascular CirculationEndothelium, VascularFemaleFluorescent Antibody TechniqueMicePeptidesProtein BindingRetinal VesselsLigandsPeptidesblood−brain barrierblood−retina barrierbrain endothelial cellspeptidephage display

Identifiers

PMID30670660
PMCPMC6369793
OpenAlexW2913970990

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.