keyword
https://read.qxmd.com/read/33854697/the-cd36-ligand-promoted-autophagy-protects-retinal-pigment-epithelial-cells-from-oxidative-stress
#41
JOURNAL ARTICLE
Marie-France Dorion, Mukandila Mulumba, Shuya Kasai, Ken Itoh, William D Lubell, Huy Ong
The retinal pigment epithelium (RPE) performs many functions that maintain photoreceptor health. Oxidative damage to the RPE is a critical component in the pathogenesis of eye diseases such as age-related macular degeneration (AMD). Ligands of the cluster of differentiation 36 (CD36) have previously preserved photoreceptor integrity in mouse models of AMD. The cytoprotective effect of the CD36 ligand MPE-001 on RPE cells has now been elucidated employing a model of oxidative stress. Sodium iodate (NaIO3 ) induced formation of reactive oxygen species and apoptosis in human RPE cells, which were decreased by MPE-001 without affecting antioxidant enzyme transcription...
2021: Oxidative Medicine and Cellular Longevity
https://read.qxmd.com/read/33788833/analysis-of-the-snare-stx8-recycling-reveals-that-the-retromer-sorting-motif-has-undergone-evolutionary-divergence
#42
JOURNAL ARTICLE
Francisco Yanguas, M-Henar Valdivieso
Fsv1/Stx8 is a Schizosaccharomyces pombe protein similar to mammalian syntaxin 8. stx8Δ cells are sensitive to salts, and the prevacuolar endosome (PVE) is altered in stx8Δ cells. These defects depend on the SNARE domain, data that confirm the conserved function of syntaxin8 and Stx8 in vesicle fusion at the PVE. Stx8 localizes at the trans-Golgi network (TGN) and the prevacuolar endosome (PVE), and its recycling depends on the retromer component Vps35, and on the sorting nexins Vps5, Vps17, and Snx3. Several experimental approaches demonstrate that Stx8 is a cargo of the Snx3-retromer...
March 31, 2021: PLoS Genetics
https://read.qxmd.com/read/33783314/the-bax-binding-protein-moap1-associates-with-lc3-and-promotes-closure-of-the-phagophore
#43
JOURNAL ARTICLE
Hao-Chun Chang, Ran N Tao, Chong Teik Tan, Ya Jun Wu, Boon Huat Bay, Victor C Yu
MOAP1 (modulator of apoptosis 1) is a BAX-binding protein tightly regulated by the ubiquitin-proteasome system. Apoptotic stimuli stabilize MOAP1 protein and facilitate its interaction with BAX to promote apoptosis. Here we show that in contrast to being resistant to apoptotic stimuli, MOAP1-deficient cells are hypersensitive to cell death mediated by starvation rendered by EBSS treatment. MOAP1-deficient cells exhibited impairment in macroautophagy/autophagy signaling induced by EBSS. Mechanistic analysis revealed that MOAP1-deficient cells had no notable defect in the recruitment of the pre-autophagosomal phosphatidylinositol-3-phosphate (PtdIns3P)-binding proteins, ZFYVE1/DFCP1 and WIPI2, nor in the LC3 lipidation mechanism regulated by the ATG12-ATG5-ATG16L1 complex upon EBSS treatment...
March 30, 2021: Autophagy
https://read.qxmd.com/read/33779513/tnf-induced-necroptosis-initiates-early-autophagy-events-via-ripk3-dependent-ampk-activation-but-inhibits-late-autophagy
#44
JOURNAL ARTICLE
Wenxian Wu, Xiaojing Wang, Yadong Sun, Niklas Berleth, Jana Deitersen, David Schlütermann, Fabian Stuhldreier, Nora Wallot-Hieke, María José Mendiburo, Jan Cox, Christoph Peter, Ann Kathrin Bergmann, Björn Stork
Macroautophagy/autophagy and necroptosis represent two opposing cellular s tress responses. Whereas autophagy primarily fulfills a cyto-protective function, necroptosis is a form of regulated cell death induced via death receptors. Here, we aimed at investigating the molecular crosstalk between these two pathways. We observed that RIPK3 directly associates with AMPK and phosphorylates its catalytic subunit PRKAA1/2 at T183/T172. Activated AMPK then phosphorylates the autophagy-regulating proteins ULK1 and BECN1...
March 28, 2021: Autophagy
https://read.qxmd.com/read/33779490/condition-dependent-functional-shift-of-two-drosophila-mtmr-lipid-phosphatases-in-autophagy-control
#45
JOURNAL ARTICLE
Anna Manzéger, Kinga Tagscherer, Péter Lőrincz, Henrik Szaker, Tamás Lukácsovich, Petra Pilz, Regina Kméczik, George Csikós, Miklós Erdélyi, Miklós Sass, Tibor Kovács, Tibor Vellai, Viktor A Billes
Myotubularin (MTM) and myotubularin-related (MTMR) lipid phosphatases catalyze the removal of a phosphate group from certain phosphatidylinositol derivatives. Because some of these substrates are required for macroautophagy/autophagy, during which unwanted cytoplasmic constituents are delivered into lysosomes for degradation, MTM and MTMRs function as important regulators of the autophagic process. Despite its physiological and medical significance, the specific role of individual MTMR paralogs in autophagy control remains largely unexplored...
March 28, 2021: Autophagy
https://read.qxmd.com/read/33760868/legionella-hijacks-the-host-golgi-to-er-retrograde-pathway-for-the-association-of-legionella-containing-vacuole-with-the-er
#46
JOURNAL ARTICLE
Mio Kawabata, Honoka Matsuo, Takumi Koito, Misaki Murata, Tomoko Kubori, Hiroki Nagai, Mitsuo Tagaya, Kohei Arasaki
Legionella pneumophila (L. pneumophila) is a gram-negative bacterium that replicates in a compartment that resembles the host endoplasmic reticulum (ER). To create its replicative niche, L. pneumophila manipulates host membrane traffic and fusion machineries. Bacterial proteins called Legionella effectors are translocated into the host cytosol and play a crucial role in these processes. In an early stage of infection, Legionella subverts ER-derived vesicles (ERDVs) by manipulating GTPase Rab1 to facilitate remodeling of the Legionella-containing vacuole (LCV)...
March 2021: PLoS Pathogens
https://read.qxmd.com/read/33706935/amyloidogenic-and-anti-amyloidogenic-properties-of-presenilin-1
#47
JOURNAL ARTICLE
Victor Bustos, Maria V Pulina, Jose Ledo
Presenilin 1 (PS1) is an intramembrane protease, the active subunit of the γ-secretase complex. Its well-studied function is the amyloidogenic cleavage of the C-terminal fragment of the amyloid precursor protein, also known as C99, to produce the Abeta peptide. Recent findings from the Greengard laboratory suggest that PS1 also have anti-amyloidogenic activities, which reduce Abeta levels. First, it redirects APP-C99 toward autophagic degradation, lowering the amount that can be converted into Abeta. The protein kinase CK1γ2 phosphorylates PS1 at Ser367...
2021: Advances in Pharmacology
https://read.qxmd.com/read/33661178/secondary-leukemia-in-a-patient-with-ebv-hlh-carrying-heterozygous-stxbp2-variant
#48
JOURNAL ARTICLE
Meiling Liao, Jie Yu
Hemophagocytic lymphohistiocytosis (HLH) is a symptom with severe systemic hyperinflammation. A 26-month-old male presented with Epstein-Barr virus associated HLH with a heterozygous variant of syntaxin-binding protein-2 (STXBP2). Complete remission was achieved with the HLH-2004 protocol, but the disease soon relapsed. Four weeks after re-installing HLH-2004 protocol, HLH was resolved. The cumulative dosage of etoposide was 2100 mg/m2. He developed acute promyelocytic leukemia 17 months later. The patient underwent standard chemotherapy and since remained in complete remission...
March 3, 2021: Journal of Pediatric Hematology/oncology
https://read.qxmd.com/read/33632058/c9orf72-als-ftd-recent-evidence-for-dysregulation-of-the-autophagy-lysosome-pathway-at-multiple-levels
#49
REVIEW
Jimmy Beckers, Arun Kumar Tharkeshwar, Philip Van Damme
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are two clinically distinct classes of neurodegenerative disorders. Yet, they share a range of genetic, cellular, and molecular features. Hexanucleotide repeat expansions (HREs) in the C9orf72 gene and the accumulation of toxic protein aggregates in the nervous systems of the affected individuals are among such common features. Though the mechanisms by which HREs cause toxicity is not clear, the toxic gain of function due to transcribed HRE RNA or dipeptide repeat proteins (DPRs) produced by repeat-associated non-AUG translation together with a reduction in C9orf72 expression are proposed as the contributing factors for disease pathogenesis in ALS and FTD...
November 2021: Autophagy
https://read.qxmd.com/read/33550611/the-equine-graying-with-age-mutation-of-the-stx17-gene-a-copy-number-study-using-droplet-digital-pcr-reveals-a-new-pattern
#50
JOURNAL ARTICLE
J Nowacka-Woszuk, M Mackowski, M Stefaniuk-Szmukier, J Cieslak
The equine graying with age causative mutation in the syntaxin-17 gene (STX17) has been known for over a decade, but proper genotyping of this variant remains challenging due to its molecular character (4.6-kb tandem duplication). Precise information on gray mutation status is important for horse breeders and veterinarians, since gray homozygous horses are more prone to developing aggressive melanoma tumors than heterozygotes. Since recent studies have confirmed that droplet digital PCR is a valuable technique for copy number analysis, we decided to investigate whether this method can be used for accurate genotyping of the horse graying-related variant and established the copy numbers of the 4...
February 7, 2021: Animal Genetics
https://read.qxmd.com/read/33417719/the-panel-of-syntaxin-1-and-insulinoma-associated-protein-1-outperforms-classic-neuroendocrine-markers-in-pulmonary-neuroendocrine-neoplasms
#51
JOURNAL ARTICLE
Tamás Zombori, Sándor Turkevi-Nagy, Anita Sejben, Gréta Juhász-Nagy, Gábor Cserni, József Furák, László Tiszlavicz, László Krenács, Bence Kővári
AIM: Syntaxin-1 (STX1) is a recently described highly sensitive and specific neuroendocrine marker. We evaluated the applicability of STX1 as an immunohistochemical marker in pulmonary neuroendocrine neoplasms (NENs). We compared STX1 with established neuroendocrine markers, including insulinoma-associated protein 1 (INSM1). EXPERIMENTAL DESIGN: Typical carcinoids (n = 33), atypical carcinoids (n = 7), small cell lung carcinomas ([SCLCs] n = 30), and large cell neuroendocrine lung carcinomas (n = 17) were immunostained using tissue microarray for STX1, chromogranin-A, synaptophysin, CD56, and INSM1...
January 8, 2021: APMIS: Acta Pathologica, Microbiologica, et Immunologica Scandinavica
https://read.qxmd.com/read/33336726/circular-rna-circ_0000034-upregulates-stx17-level-to-promote-human-retinoblastoma-development-via-inhibiting-mir-361-3p
#52
JOURNAL ARTICLE
H Liu, H-F Yuan, D Xu, K-J Chen, N Tan, Q-J Zheng
OBJECTIVE: Retinoblastoma (RB) is a common intraocular tumor of infancy and childhood. Circular RNAs (circRNAs) are related to the development of RB. The purpose of this research was to reveal the functional mechanism of circRNA circ_0000034 in RB. MATERIALS AND METHODS: Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) and Western blot were applied to determine the levels of genes. MTT assay and flow cytometry were employed to assess cell proliferation and apoptosis rate, respectively...
December 2020: European Review for Medical and Pharmacological Sciences
https://read.qxmd.com/read/33191543/a-snare-protein-syntaxin-17-captures-cftr-to-potentiate-autophagosomal-clearance-under-stress
#53
JOURNAL ARTICLE
Kavisha Arora, Pramodha Liyanage, Qing Zhong, Anjaparavanda P Naren
Autophagy, a cellular stress response to starvation and bacterial infection, is executed by double-membrane-bound organelles called autophagosomes. Autophagosomes transfer cytosolic material to acidified lysosomes for degradation following soluble N-ethylmaleimide-sensitive factor attachment receptor (SNARE)-dependent fusion processes. Many of the autophagy-related disorders stem from defective end-step proteolysis inside lysosomes. The role of epithelial cystic fibrosis (CF) transmembrane conductance regulator (CFTR) chloride channel has been argued to be critical for efficient lysosomal clearance; however, its context to autophagic clearance and the underlying mechanism is poorly defined...
February 2021: FASEB Journal: Official Publication of the Federation of American Societies for Experimental Biology
https://read.qxmd.com/read/33155266/long-non-coding-rna-xist-confers-aggressive-progression-via-mir-361-3p-stx17-in-retinoblastoma-cells
#54
JOURNAL ARTICLE
L-L Yang, Q Li, X Zhang, T Cao
OBJECTIVE: Retinoblastoma (RB) is a frequent intraocular tumor in children. Long-non-coding RNA X inactive specific transcript (XIST) has been reported to participate in the RB process, while its potential role remains largely unknown. PATIENTS AND METHODS: The expression patterns of XIST, microRNA (miR)-361-3p, and Syntaxin 17 (STX17) were determined using quantitative Real Time-Polymerase Chain Reaction (qRT-PCR) assay. 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT), flow cytometry, and transwell assays were employed to reckon cell viability, apoptosis, and mobility in RB cells, respectively...
October 2020: European Review for Medical and Pharmacological Sciences
https://read.qxmd.com/read/33112705/ptpn9-mediated-dephosphorylation-of-vti1b-promotes-atg16l1-precursor-fusion-and-autophagosome-formation
#55
JOURNAL ARTICLE
He-Yen Chou, Yi-Tang Lee, Yuchieh Jay Lin, Jung-Kun Wen, Wen-Hsin Peng, Pei-Lien Hsieh, Shu-Yu Lin, Chin-Chun Hung, Guang-Chao Chen
Macroautophagy/autophagy is an evolutionarily conserved intracellular pathway for the degradation of cytoplasmic materials. Under stress conditions, autophagy is upregulated and double-membrane autophagosomes are formed by the expansion of phagophores. The ATG16L1 precursor fusion contributes to development of phagophore structures and is critical for the biogenesis of autophagosomes. Here, we discovered a novel role of the protein tyrosine phosphatase PTPN9 in the regulation of homotypic ATG16L1 vesicle fusion and early autophagosome formation...
October 28, 2020: Autophagy
https://read.qxmd.com/read/33077556/an-autophagy-dependent-tubular-lysosomal-network-synchronizes-degradative-activity-required-for-muscle-remodeling
#56
JOURNAL ARTICLE
Tadayoshi Murakawa, Amy A Kiger, Yuriko Sakamaki, Mitsunori Fukuda, Naonobu Fujita
Lysosomes are compartments for the degradation of both endocytic and autophagic cargoes. The shape of lysosomes changes with cellular degradative demands, however, there is limited knowledge about the mechanisms or significance that underlies distinct lysosomal morphologies. Here, we found an extensive tubular autolysosomal network in Drosophila abdominal muscle remodeling during metamorphosis. The tubular network transiently appeared and exhibited the capacity to degrade autophagic cargoes. The tubular autolysosomal network was uniquely marked by the autophagic SNARE protein, Syntaxin 17, and its formation depended on both autophagic flux and degradative function, with the exception of the Atg12 and Atg8 ubiquitin-like conjugation systems...
October 19, 2020: Journal of Cell Science
https://read.qxmd.com/read/32828953/syntaxin-17-inhibits-ischemic-neuronal-injury-by-resuming-autophagy-flux-and-ameliorating-endoplasmic-reticulum-stress
#57
JOURNAL ARTICLE
Lei Chen, Yun-Fei Xia, Shu-Fang Shen, Jie Tang, Jia-Li Chen, Ke Qian, Zhong Chen, Zheng-Hong Qin, Rui Sheng
Previous studies have shown that syntaxin 17 (STX17) is involved in mediating the fusion of autophagosomes and lysosomes. This study aimed to investigate the role and mechanism of STX17 in neuronal injury following cerebral ischemia/reperfusion. The ischemia/reperfusion (I/R) models were established by transient middle cerebral artery occlusion (tMCAO) in mice and oxygen glucose deprivation/reperfusion (O/R) in primary cultured cortical neurons and HT22 cells. Cerebral ischemia/reperfusion significantly up-regulated the expression of STX17 in neurons...
November 20, 2020: Free Radical Biology & Medicine
https://read.qxmd.com/read/32467992/hyperoxia-reduces-stx17-expression-and-inhibits-the-autophagic-flux-in-alveolar-type-ii-epithelial-cells-in-newborn-rats
#58
JOURNAL ARTICLE
Dan Zhang, Xinyi Zhao, Dingning Zhang, Siyang Gao, Xindong Xue, Jianhua Fu
Supplemental oxygen therapy can be life‑saving for premature infants. Our previous study revealed a defect in the autophagic flux in the lung tissues of neonatal rats with hyperoxia‑induced bronchopulmonary dysplasia (BPD), but the underlying mechanism remains unknown. Moreover, there are few innovative treatments that can completely alter the course of BPD. The present study examined the expression of Syntaxin 17 (STX17), a protein necessary for autophagosome‑lysosome binding, in alveolar type II (AT‑II) epithelial cells of neonatal rats with BPD...
May 27, 2020: International Journal of Molecular Medicine
https://read.qxmd.com/read/32324083/autophagy-triggers-ctsd-cathepsin-d-maturation-and-localization-inside-cells-to-promote-apoptosis
#59
JOURNAL ARTICLE
Yu-Qin Di, Xiao-Lin Han, Xin-Le Kang, Di Wang, Cai-Hua Chen, Jin-Xing Wang, Xiao-Fan Zhao
CTSD/CathD/CATD (cathepsin D) is a lysosomal aspartic protease. A distinguishing characteristic of CTSD is its dual functions of promoting cell proliferation via secreting a pro-enzyme outside the cells as a ligand, and promoting apoptosis via the mature form of this enzyme inside cells; however, the regulation of its secretion, expression, and maturation is undetermined. Using the lepidopteran insect Helicoverpa armigera , a serious agricultural pest, as a model, we revealed the dual functions and regulatory mechanisms of CTSD secretion, expression, and maturation...
May 2021: Autophagy
https://read.qxmd.com/read/32264736/acetylation-of-stx17-syntaxin-17-controls-autophagosome-maturation
#60
JOURNAL ARTICLE
Qiuhong Shen, Yin Shi, Jiaqi Liu, Hua Su, Jingtao Huang, Yi Zhang, Chao Peng, Tianhua Zhou, Qiming Sun, Wei Wan, Wei Liu
The fusion of autophagosomes and endosomes/lysosomes, also called autophagosome maturation, ensures the degradation of autophagic cargoes. It is an important regulatory step of the macroautophagy/autophagy process. STX17 is the key autophagosomal SNARE protein that mediates autophagosome maturation. Here, we report that the acetylation of STX17 regulates its SNARE activity and autophagic degradation. The histone acetyltransferase CREBBP/CBP and the deacetylase HDAC2 specifically regulate the acetylation of STX17...
April 7, 2020: Autophagy
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