Evidence map›Paper›PMID 28598240›Full record

ArticleAutophagy2017

Classical autophagy proteins LC3B and ATG4B facilitate melanosome movement on cytoskeletal tracks.

Amrita Ramkumar, Divya Murthy, Desingu Ayyappa Raja, Archana Singh, Anusha Krishnan, Sangeeta Khanna, Archana Vats, Lipi Thukral, Pushkar Sharma, Sridhar Sivasubbu and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.1field-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

30 citing papers in PubMed, 74 citations in OpenAlex.

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  16. The Immunogenetics of Alopecia areata.Advances in experimental medicine and biology · 2022
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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

13 authors at 3 institutions in 1 country.

Amrita Ramkumara CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Divya Murthya CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Desingu Ayyappa Rajaa CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Archana Singha CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Anusha Krishnana CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Sangeeta Khannaa CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Archana Vatsa CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Lipi Thukrala CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Pushkar Sharmac National Institute of Immunology , Aruna Asaf Ali Marg, New Delhi , India.
Sridhar Sivasubbua CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Rajni Ranic National Institute of Immunology , Aruna Asaf Ali Marg, New Delhi , India.
Vivek T Natarajana CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Rajesh S Gokhalea CSIR- Institute of Genomics and Integrative Biology , Mathura Road, New Delhi , India.
Institute of Genomics and Integrative Biology · INNational Institute of Immunology · INAcademy of Scientific and Innovative Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macroautophagy/autophagy is a dynamic and inducible catabolic process that responds to a variety of hormonal and environmental cues. Recent studies highlight the interplay of this central pathway in a variety of pathophysiological diseases. Although defective autophagy is implicated in melanocyte proliferation and pigmentary disorders, the mechanistic relationship between the 2 pathways has not been elucidated. In this study, we show that autophagic proteins LC3B and ATG4B mediate melanosome trafficking on cytoskeletal tracks. While studying melanogenesis, we observed spatial segregation of LC3B-labeled melanosomes with preferential absence at the dendritic ends of melanocytes. This LC3B labeling of melanosomes did not impact the steady-state levels of these organelles but instead facilitated their intracellular positioning. Melanosomes primarily traverse on microtubule and actin cytoskeletal tracks and our studies reveal that LC3B enables the assembly of microtubule translocon complex. At the microtubule-actin crossover junction, ATG4B detaches LC3B from melanosomal membranes by enzymatic delipidation. Further, by live-imaging we show that melanosomes transferred to keratinocytes lack melanocyte-specific LC3B. Our study thus elucidates a new role for autophagy proteins in directing melanosome movement and reveal the unconventional use of these proteins in cellular trafficking pathways. Such crosstalk between the central cellular function and housekeeping pathway may be a crucial mechanism to balance melanocyte bioenergetics and homeostasis.

Indexed as

AutophagyMovementActin CytoskeletonAnimalsAutophagy-Related ProteinsCysteine EndopeptidasesCytoskeletonDendritesGene Knockdown TechniquesHumansKeratinocytesLipidsMelanocytesMelanoma, ExperimentalMelanosomesMice, Inbred C57BLAtg4b protein, mouseAutophagy-Related ProteinsCysteine EndopeptidasesLipidsMap1lc3b protein, mouseMicrotubule-Associated Proteinsautophagycytoskeletonmelanosomesmicrotubulestrafficking

Identifiers

PMID28598240
PMCPMC5584859
OpenAlexW2621753584

What OpenQuestion 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 OpenQuestion graph.