Evidence map›Paper›PMID 33884901›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2021

Membranous Structures Directly Come in Contact With p62/SQSTM1 Bodies.

Isei Tanida, Tomohiro Haruta, Mitsuo Suga, Shunsuke Takei, Akira Takebe, Yoko Furuta, Junji Yamaguchi, Juan Alejandro Oliva Trejo, Soichiro Kakuta, Yasuo Uchiyama

Open access · bronzeAbstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 3 institutions in 1 country.

Isei TanidaDepartment of Cellular and Molecular Neuropathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Tomohiro HarutaBio 3D Promotion Group, JEOL Ltd., Tokyo, Japan.
Mitsuo SugaBio 3D Promotion Group, JEOL Ltd., Tokyo, Japan.
Shunsuke TakeiHealthcare Business Unit, Nikon Corporation, Yokohama, Japan.
Akira TakebeJEOL-Nikon CLEM Solution Center, Tokyo, Japan.
Yoko FurutaDepartment of Cellular and Molecular Neuropathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Junji YamaguchiDepartment of Cellular and Molecular Neuropathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Juan Alejandro Oliva TrejoDepartment of Cellular and Molecular Neuropathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Soichiro KakutaDepartment of Cellular and Molecular Neuropathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Yasuo UchiyamaDepartment of Cellular and Molecular Neuropathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Juntendo University · JPJEOL (Japan) · JPNikon (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During autophagy, autophagosomes are formed to engulf cytoplasmic contents. p62/SQSTM-1 is an autophagic adaptor protein that forms p62 bodies. A unique feature of p62 bodies is that they seem to directly associate with membranous structures. We first investigated the co-localization of mKate2-p62 bodies with phospholipids using click chemistry with propargyl-choline. Propargyl-choline-labeled phospholipids were detected inside the mKate2-p62 bodies, suggesting that phospholipids were present inside the bodies. To clarify whether or not p62 bodies come in contact with membranous structures directly, we investigated the ultrastructures of p62 bodies using in-resin correlative light and electron microscopy of the Epon-embedded cells expressing mKate2-p62. Fluorescent-positive p62 bodies were detected as uniformly lightly osmificated structures by electron microscopy. Membranous structures were detected on and inside the p62 bodies. In addition, multimembranous structures with rough endoplasmic reticulum-like structures that resembled autophagosomes directly came in contact with amorphous-shaped p62 bodies. These results suggested that p62 bodies are unique structures that can come in contact with membranous structures directly.

Indexed as

AutophagyAutophagosomesCell Membrane StructuresEndoplasmic ReticulumHeLa CellsHumansPhospholipidsSequestosome-1 ProteinPhospholipidsSequestosome-1 ProteinSQSTM1 protein, humanclick chemistryin-resin CLEMpropargyl-cholineselective autophagy

Identifiers

PMID33884901
PMCPMC8182640
OpenAlexW3153390482

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.