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Membranous Structures Directly Come in Contact With p62/SQSTM1 Bodies
- Source :
- J Histochem Cytochem
- Publication Year :
- 2021
- Publisher :
- SAGE Publications, 2021.
-
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
- Subjects :
- 0301 basic medicine
Histology
Chemistry
Autophagy
Autophagosomes
Signal transducing adaptor protein
Articles
Endoplasmic Reticulum
Cell Membrane Structures
Cell biology
Selective autophagy
03 medical and health sciences
030104 developmental biology
0302 clinical medicine
Feature (computer vision)
Cytoplasm
Sequestosome-1 Protein
Humans
Anatomy
Phospholipids
030217 neurology & neurosurgery
HeLa Cells
Subjects
Details
- ISSN :
- 15515044 and 00221554
- Volume :
- 69
- Database :
- OpenAIRE
- Journal :
- Journal of Histochemistry & Cytochemistry
- Accession number :
- edsair.doi.dedup.....eaea4f43da041c6d72f89357e07fbc54
- Full Text :
- https://doi.org/10.1369/00221554211011423