Evidence map›Paper›PMID 32752027›Full record

ArticleInternational journal of molecular sciences2020

The Impact of Small Extracellular Vesicles on Lymphoblast Trafficking across the Blood-Cerebrospinal Fluid Barrier In Vitro.

Ulrike Erb, Julia Hikel, Svenja Meyer, Hiroshi Ishikawa, Thomas S Worst, Katja Nitschke, Philipp Nuhn, Stefan Porubsky, Christel Weiss, Horst Schroten and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 35% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. 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

12 authors at 3 institutions in 2 countries.

Ulrike ErbDepartment of Pediatrics, University Medical Center Mannheim, 68167 Mannheim, Germany.
Julia HikelDepartment of Pediatrics, University Medical Center Mannheim, 68167 Mannheim, Germany.
Svenja MeyerDepartment of Pediatrics, University Medical Center Mannheim, 68167 Mannheim, Germany.
Hiroshi IshikawaLaboratory of Clinical Regenerative Medicine, Department of Neurosurgery, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8575, Japan.
Thomas S WorstDepartment of Urology and Urosurgery, University Medical Center Mannheim, 68167 Mannheim, Germany.
Katja NitschkeDepartment of Urology and Urosurgery, University Medical Center Mannheim, 68167 Mannheim, Germany.
Philipp NuhnDepartment of Urology and Urosurgery, University Medical Center Mannheim, 68167 Mannheim, Germany.
Stefan PorubskyInstitute of Pathology, University Medical Center of the Johannes Gutenberg University Mainz, 55101 Mainz, Germany.
Christel WeissDepartment of Medical Statistics and Biomathematics, University Medical Center Mannheim, 68167 Mannheim, Germany.
Horst SchrotenDepartment of Pediatrics, University Medical Center Mannheim, 68167 Mannheim, Germany.
Rüdiger AdamDepartment of Pediatrics, University Medical Center Mannheim, 68167 Mannheim, Germany.
Michael KarremannDepartment of Pediatrics, University Medical Center Mannheim, 68167 Mannheim, Germany.ORCID 0000-0002-9961-4752
Heidelberg University · DEJohannes Gutenberg University Mainz · DEUniversity of Tsukuba · JP

Funding

DLFH Aktion für Krebskranke Kinder Mannheim n.a.mcon goes golf n.a.
6 · The paper itself

Abstract

Central nervous System (CNS) disease in pediatric acute lymphoblastic leukemia (ALL) is a major concern, but still, cellular mechanisms of CNS infiltration are elusive. The choroid plexus (CP) is a potential entry site, and, to some extent, invasion resembles CNS homing of lymphocytes during healthy state. Given exosomes may precondition target tissue, the present work aims to investigate if leukemia-derived exosomes contribute to a permissive phenotype of the blood-cerebrospinal fluid barrier (BCSFB). Leukemia-derived exosomes were isolated by ultracentrifugation from the cell lines SD-1, Nalm-6, and P12-Ichikawa (P12). Adhesion and uptake to CP epithelial cells and the significance on subsequent ALL transmigration across the barrier was studied in a human BCSFB in vitro model based on the HiBCPP cell line. The various cell lines markedly differed regarding exosome uptake to HiBCPP and biological significance. SD-1-derived exosomes associated to target cells unspecifically without detectable cellular effects. Whereas Nalm-6 and P12-derived exosomes incorporated by dynamin-dependent endocytosis, uptake in the latter could be diminished by integrin blocking. In addition, only P12-derived exosomes led to facilitated transmigration of the parental leukemia cells. In conclusion, we provide evidence that, to a varying extent, leukemia-derived exosomes may facilitate CNS invasion of ALL across the BCSFB without destruction of the barrier integrity.

Indexed as

AnimalsBlood-Brain BarrierCell AdhesionCell Line, TumorCell MovementCentral Nervous System DiseasesChoroid PlexusEndocytosisEpithelial CellsExtracellular VesiclesHematopoietic Stem CellsHumansLymphocytesNeoplasm InvasivenessPrecursor Cell Lymphoblastic Leukemia-LymphomaProtein Transportcentral nervous system infiltrationchoroid plexusexosomespediatric acute lymphoblastic leukemia

Identifiers

PMID32752027
PMCPMC7432056
OpenAlexW3046293447

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.