Evidence map›Paper›PMID 32524725›Full record

ArticleCytoskeleton (Hoboken, N.J.)2020

Lis1 co-localizes with actin in the phagocytic cup and regulates phagocytosis.

Aditya Chhatre, Paulomi Sanghavi, Roop Mallik

Open access · greenAbstract read
In one paragraph

Article in Cytoskeleton (Hoboken, N.J.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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  4. 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

3 authors at 1 institution in 1 country.

Aditya ChhatreDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Paulomi SanghaviDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Roop MallikDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Tata Institute of Fundamental Research · IN

Funding

DBT-Wellcome Trust India Alliance IA/E/15/1/502298DBT-Wellcome Trust India Alliance IA/S/19/2/504634Wellcome Trust 079214Wellcome Trust WT079214MA
6 · The paper itself

Abstract

Phagocytosis, the ingestion of solid particles by cells is essential for nutrient uptake, innate immune response, antigen presentation and organelle homeostasis. Here we show that Lissencephaly-1 (Lis1), a well-known regulator of the microtubule motor dynein, co-localizes with actin at the phagocytic cup in the early stages of phagocytosis. Both knockdown and overexpression of Lis1 perturb phagocytosis, suggesting that Lis1 levels may be regulated during particle engulfment to facilitate remodeling of actin filaments within the phagocytic cup. This requirement of Lis1 is replicated in mouse macrophage cells as well as in the amoeba Dictyostelium, indicating an evolutionarily conserved role for Lis1 in phagocytosis. In support of these findings, Dictyostelium cells overexpressing Lis1 show defects in migration possibly caused by dysregulated actin. Taken together, Lis1 localizes to the phagocytic cup and influences the actin cytoskeleton in a manner that appears important for the uptake of solid particles into cells.

Indexed as

1-Alkyl-2-acetylglycerophosphocholine EsteraseActinsAnimalsDictyosteliumHEK293 CellsHumansMiceMicrotubule-Associated ProteinsPhagocytosisRAW 264.7 Cells1-Alkyl-2-acetylglycerophosphocholine EsteraseActinsMicrotubule-Associated ProteinsPAFAH1B1 protein, humanPafah1b1 protein, mouseactin dynamicslatex bead phagosomeLis1Lissencephalyphagocytosis

Identifiers

PMID32524725
PMCPMC7611227
OpenAlexW3033932742

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.