LAMP3 inhibits autophagy and contributes to cell death by lysosomal membrane permeabilization

Tsutomu Tanaka(National Institutes of Health), Blake M. Warner(National Institutes of Health), Drew G. Michael(National Institutes of Health), Hiroyuki Nakamura(National Institutes of Health), Toshio Odani(National Institutes of Health), Hongen Yin(National Institutes of Health), Tatsuya Atsumi(Hokkaido University), Masayuki Noguchi(Hokkaido University), John A. Chiorini(National Institutes of Health)
Autophagy
November 22, 2021
Cited by 111Open Access
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Abstract

ABBREVIATIONS: A253-control: A253 control for LAMP3 stable overexpression; A253- LAMP3: A253 LAPM3 stable overexpression; CASP1: caspase 1; CASP3: caspase 3; CHX: cycloheximide; CTSB: cathepsin B; CTSD: cathepsin D; CQ: chloroquine; DCs: dendritic cells; ER: endoplasmic reticulum; LGALS3: galectin 3; HCV: hepatitis C virus; HSG-control: HSG control for LAMP3 stable overexpression; HSG-LAMP3: HSG LAMP3 stable overexpression; HSP: heat shock protein; HTLV-1: human T-lymphocyte leukemia virus-1; IXA: ixazomib; LAMP: lysosomal associated membrane protein; MHC: major histocompatibility complex; mAb: monoclonal antibody; OE: overexpression; pepA: pepstatin A; pAb: polyclonal antibody; pSS: primary Sjögren syndrome; qRT-PCR: quantitative real- time reverse transcriptase polymerase chain reaction; SLE: systemic lupus erythematosus; SS: Sjögren syndrome; UPR: unfolded protein response; V-ATPase: vacuolar-type proton- translocating ATPase; Y-VAD: Ac-YVAD-cmk; Z-DEVD; Z-DEVD-fmk; Z-VAD: Z-VAD- fmk.


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