Evidence map›Paper›PMID 25575683›Full record

ArticleMolecular neurobiology2016

Migration and Phagocytic Ability of Activated Microglia During Post-natal Development is Mediated by Calcium-Dependent Purinergic Signalling.

Aditya Sunkaria, Supriya Bhardwaj, Avishek Halder, Aarti Yadav, Rajat Sandhir

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
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  11. The Safeguarding Microglia: Central Role for P2YFrontiers in pharmacology · 2020
    Article
  12. Article
  13. Review
  14. Article
  15. Store-Operated CaFrontiers in molecular neuroscience · 2016
    Article
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

5 authors at 2 institutions in 1 country.

Aditya SunkariaDepartment of Biochemistry, Panjab University, Chandigarh, 160014, India.
Supriya BhardwajDepartment of Dermatology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.
Avishek HalderDepartment of Biochemistry, Panjab University, Chandigarh, 160014, India.
Aarti YadavDepartment of Biochemistry, Panjab University, Chandigarh, 160014, India.
Rajat SandhirDepartment of Biochemistry, Panjab University, Chandigarh, 160014, India. sandhir@pu.ac.in.
Panjab University · INPost Graduate Institute of Medical Education and Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglia play an important role in synaptic pruning and controlled phagocytosis of neuronal cells during developmental stages. However, the mechanisms that regulate these functions are not completely understood. The present study was designed to investigate the role of purinergic signalling in microglial migration and phagocytic activity during post-natal brain development. One-day-old BALB/c mice received lipopolysaccharide (LPS) and/or a purinergic analogue (2-methylthioladenosine-5'-diphosphate; 2MeSADP), intracerebroventrically (i.c.v.). Combined administration of LPS and 2MeSADP resulted in activation of microglia as evident from increased expression of ionised calcium-binding adapter molecule 1 (Iba1). Activated microglia showed increased expression of purinergic receptors (P2Y2, P2Y6 and P2Y12). LPS either alone or in combination with 2MeSADP induced the expression of Na(+)/Ca(2+) exchanger (NCX-1) and P/Q-type Ca(2+) channels along with MARCKS-related protein (MRP), which is an integral component of cell migration machinery. In addition, LPS and 2MeSADP administration induced the expression of microglial CD11b and DAP12 (DNAX-activation protein 12), which are known to be involved in phagocytosis of neurons during development. Interestingly, administration of thapsigargin (TG), a specific Ca(2+)-ATPase inhibitor of endoplasmic reticulum, prevented the LPS/2MeSADP-induced microglial activation and migration by down-regulating the expression of Iba1 and MRP, respectively. Moreover, TG also reduced the LPS/2MeSADP-induced expression of CD11b/DAP12. Taken together, the findings reveal for the first time that Ca(2+)-mediated purinergic receptors regulate the migration and phagocytic ability of microglia during post-natal brain development.

Indexed as

Cell MovementPhagocytosisSignal TransductionAdaptor Proteins, Signal TransducingAdenosine DiphosphateAnimalsAnimals, NewbornBrainCalciumCD11b AntigenCytoskeletonFemaleIntracellular SpaceLipopolysaccharidesMaleMice, Inbred BALB CAdaptor Proteins, Signal TransducingAdenosine DiphosphateCalciumCD11b AntigenLipopolysaccharidesReceptors, PurinergicTyrobp protein, mouseBrain developmentCalciumDAP12MicrogliaPhagocytosisPurinergic receptors

Identifiers

PMID25575683
OpenAlexW2029162596

What Socratic 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 Socratic graph.