Membranous Structures Directly Come in Contact With p62/SQSTM1
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Authors: | Isei Tanida Tomohiro Haruta Mitsuo Suga Shunsuke Takei Akira Takebe Yoko Furuta Junji Yamaguchi Juan Alejandro Oliva Trejo Soichiro Kakuta Yasuo Uchiyama |
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Affiliation: | Department of Cellular and Molecular Neuropathology, Graduate School of Medicine, Juntendo University, Tokyo, Japan;Bio 3D Promotion Group, JEOL Ltd., Tokyo, Japan;Healthcare Business Unit, Nikon Corporation, Yokohama, Japan;JEOL-Nikon CLEM Solution Center, Tokyo, Japan;Laboratory of Morphology and Image Analysis, Research Support Center, Graduate School of Medicine, Juntendo University, Tokyo, Japan |
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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: |
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Keywords: | click chemistry in-resin CLEM propargyl-choline selective autophagy |
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