Evidence map›Paper›PMID 35085696›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2022

Particle uptake driven phagocytosis in macrophages and neutrophils enhances bacterial clearance.

Preeti Sharma, Anjali Vijaykumar, Jayashree Vijaya Raghavan, Supriya Rajendra Rananaware, Alakesh Alakesh, Janhavi Bodele, Junaid Ur Rehman, Shivani Shukla, Virta Wagde, Savitha Nadig and 5 more

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 42 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

15 authors at 1 institution in 1 country.

Preeti SharmaCentre for BioSystems Science and Engineering, Indian Institute of Science, Bengaluru 560012, India.
Anjali VijaykumarCentre for BioSystems Science and Engineering, Indian Institute of Science, Bengaluru 560012, India.
Jayashree Vijaya RaghavanCentre for BioSystems Science and Engineering, Indian Institute of Science, Bengaluru 560012, India.
Supriya Rajendra RananawareDepartment of Biochemistry, Indian Institute of Science, Bengaluru 560012, India.
Alakesh AlakeshCentre for BioSystems Science and Engineering, Indian Institute of Science, Bengaluru 560012, India.
Janhavi BodeleCentre for BioSystems Science and Engineering, Indian Institute of Science, Bengaluru 560012, India.
Junaid Ur RehmanCentre for BioSystems Science and Engineering, Indian Institute of Science, Bengaluru 560012, India.
Shivani ShuklaCentre for BioSystems Science and Engineering, Indian Institute of Science, Bengaluru 560012, India.
Virta WagdeCentre for BioSystems Science and Engineering, Indian Institute of Science, Bengaluru 560012, India.
Savitha NadigMolecular Biophysics Unit, Indian Institute of Science, Bengaluru 560012, India.
Sveta ChakrabartiDepartment of Molecular Reproduction, Development and Genetics, Indian Institute of Science, Bengaluru 560012, India.
Sandhya S VisweswariahDepartment of Molecular Reproduction, Development and Genetics, Indian Institute of Science, Bengaluru 560012, India.
Dipankar NandiDepartment of Biochemistry, Indian Institute of Science, Bengaluru 560012, India.
Balasubramanian GopalMolecular Biophysics Unit, Indian Institute of Science, Bengaluru 560012, India.
Siddharth JhunjhunwalaCentre for BioSystems Science and Engineering, Indian Institute of Science, Bengaluru 560012, India. Electronic address: siddharth@iisc.ac.in.
Indian Institute of Science Bangalore · IN

Funding

DBT-Wellcome Trust India Alliance IA/I/19/1/504265Wellcome Trust
6 · The paper itself

Abstract

Humans are exposed to numerous synthetic foreign particles in the form of drug delivery systems and diagnostic agents. Specialized immune cells (phagocytes) clear these particles by phagocytosing and attempting to degrade them. The process of recognition and internalization of the particles may trigger changes in the function of phagocytes. Some of these changes, especially the ability of a particle-loaded phagocyte to take up and neutralize pathogens, remains poorly studied. Herein, we demonstrate that the uptake of non-stimulatory cargo-free particles enhances the phagocytic ability of monocytes, macrophages and neutrophils. The enhancement in phagocytic ability was independent of particle properties, such as size or the base material constituting the particle. Additionally, we show that the increased phagocytosis was not a result of cellular activation or cellular heterogeneity but was driven by changes in cell membrane fluidity and cellular compliance. A consequence of the enhanced phagocytic activity was that particulate-laden immune cells neutralize Escherichia coli (E. coli) faster in culture. Moreover, when administered in mice as a prophylactic, particulates enable faster clearance of E. coli and Staphylococcus epidermidis. Together, we demonstrate that the process of uptake induces cellular changes that favor additional phagocytic events. This study provides insights into using non-stimulatory cargo-free particles to engineer immune cell functions for applications involving faster clearance of phagocytosable abiotic and biotic material.

Indexed as

Escherichia coliNeutrophilsAnimalsMacrophagesMiceMonocytesPhagocytesPhagocytosisImmuno-modulationMicroparticleMonocyteNanoparticlePhagocyte

Identifiers

PMID35085696
PMCPMC7615985
OpenAlexW4226062048

What OpenQuestion holds

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Registered trials

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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.