Evidence map›Paper›PMID 31223642›Full record

ArticleAdvanced biosystems2018

Trapped Chromatin Fibers Damage Flowing Red Blood Cells.

Maedeh Roushan, Mehdi Jorfi, Avanish Mishra, Keith H K Wong, Julianne Jorgensen, Eric Ell, James F Markmann, Jarone Lee, Daniel Irimia

Open access · greenAbstract read
In one paragraph

Article in Advanced biosystems, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 54% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Maedeh RoushanCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA, dirimia@mgh.harvard.edu.
Mehdi JorfiCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA, dirimia@mgh.harvard.edu.
Avanish MishraCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA, dirimia@mgh.harvard.edu.
Keith H K WongCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA, dirimia@mgh.harvard.edu.
Julianne JorgensenCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA, dirimia@mgh.harvard.edu.
Eric EllCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA, dirimia@mgh.harvard.edu.
James F MarkmannDivision of Transplantation, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Jarone LeeDepartment of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Daniel IrimiaCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA, dirimia@mgh.harvard.edu.
Harvard University · US

Funding

Bio-MicroElectroMechanical Systems Resource CenterP41EB002503 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI TONER, MEHMET · 2004 to 2018
$17.4M
Neutrophil Decision Making in Confined Environments in Health and DiseaseR01GM092804 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI IRIMIA, DANIEL · 2010 to 2022
$4.3M
MGHfC Digestive Disease Summer Research ProgramR25DK103579 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BRYAN P HURLEY · 2015 to 2026
$1.2M
Transient Obstruction of Capillary Networks by Chromatin Yarns from Neutrophils in Older AdultsR21AG051082 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI IRIMIA, DANIEL · 2015 to 2016
$479k
NIA NIH HHS R21 AG051082NIBIB NIH HHS P41 EB002503NIDDK NIH HHS R25 DK103579NIGMS NIH HHS R01 GM092804
6 · The paper itself

Abstract

Neutrophils are the most abundant white blood cells in the circulation and serve antimicrobial functions. One of their antimicrobial mechanisms involves the release of neutrophil extracellular traps (NETs), long chromatin fibers decorated with antimicrobial granular proteins that contribute to the elimination of pathogens. However, the release of NETs has also been associated with disease processes. While recent research has focused on biochemical reactions catalyzed by NETs, significantly less is known about the mechanical effect of NETs in circulation. Here, microfluidic devices and biophysical models are employed to study the consequences of the interactions between NETs trapped in channels and red blood cells (RBCs) flowing in blood over the NETs. It has been found that the RBCs can be deformed and ruptured after interactions with NETs, generating RBC fragments. Significant increases in the number of RBC fragments have also been found in the circulation of patients with conditions in which NETs have been demonstrated to be present in circulation, including sepsis and kidney transplant. Further studies will probe the potential utility of RBC fragments in the diagnostic, monitoring, and treatment of diseases associated with the presence of NETs in circulation.

Indexed as

microfluidicsneutrophil extracellular trapsred blood cellsschistocytes

Identifiers

PMID31223642
PMCPMC6586417
OpenAlexW2887842728

What OpenQuestion holds

Textmetadata
LicenceTDM
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.