52 research outputs found
Phosphorylation of p62 by AMP-activated protein kinase mediates autophagic cell death in adult hippocampal neural stem cells
In the adult brain, programmed death of neural stem cells is considered to be critical for tissue homeostasis and cognitive function and is dysregulated in neurodegeneration. Previously, we have reported that adult rat hippocampal neural (HCN) stem cells undergo autophagic cell death (ACD) following insulin withdrawal. Because the apoptotic capability of the HCN cells was intact, our findings suggested activation of unique molecular mechanisms linking insulin withdrawal to ACD rather than apoptosis. Here, we report that phosphorylation of autophagy-associated protein p62 by AMP-activated protein kinase (AMPK) drives ACD and mitophagy in HCN cells. Pharmacological inhibition of AMPK or genetic ablation of the AMPK alpha 2 subunit by clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 genome editing suppressed ACD, whereas AMPK activation promoted ACD in insulin-deprived HCN cells. We found that following insulin withdrawal AMPK phosphorylated p62 at a novel site, Ser-293/Ser-294 (in rat and human p62, respectively). Phosphorylated p62 translocated to mitochondria and induced mitophagy and ACD. Interestingly, p62 phosphorylation at Ser-293 was not required for staurosporine-induced apoptosis in HCN cells. To the best of our knowledge, this is the first report on the direct phosphorylation of p62 by AMPK. Our data suggest that AMPK-mediated p62 phosphorylation is an ACD-specific signaling event and provide novel mechanistic insight into the molecular mechanisms in ACD.1
Immunocytes as a Biocarrier to Delivery Therapeutic and Imaging Contrast Agents to Tumors
Radiotherapy for cancer treatment has been used for primary or adjuvant treatment in many types of cancer, and approximately half of all cancer patients are undergoing radiation. However, ionizing radiation exposure induces genetic alterations in cancer cells and results in recruitment of monocytes/macrophages by triggering signals released from these cells. Using this characteristic of monocytes/macrophages, we have attempted to develop a biocarrier loading radiosensitizing anticancer agents that can lead to enhance the therapeutic effect of radiation in cancer treatment. The aim of this study is to demonstrate the proof of this concept. THP-1 labeled with Qdot 800 or iron oxide (IO) effectively migrated into tumors of subcutaneous mouse model and increased recruitment after ionizing radiation. Functionalized liposomes carrying a radiosensitizing anticancer agent, doxorubicin, are successfully loaded in THP-1 (THP-1-LP-Dox) with reduced cytotoxicity, and THP-1-LP-Dox also was observed in tumors after intravenous administration. Here, we report that monocytes/macrophages as a biocarrier can be used as a selective tool for amplification of the therapeutic effects on radiotherapy for human cancer treatment
μ±μ²΄ν΄λ§μ κ²½μ€κΈ°μΈν¬μ μκ°ν¬μνμμμ AMPKμ μκ°ν¬μνμ μ‘° μ μλ‘μ μν
AMP-activated protein kinase (AMPK) is a well-studied molecule for the control of cellular metabolism. In addition, AMPK can affect autophagy to sustain homeostasis. Adult hippocampal neural stem (HCN) cells undergo autophagic cell death (ACD) without apoptotic features following insulin withdrawal, therefore, insulin-deprived HCN cells are regarded as a genuine model for studying autophagy and cell death-related signaling mechanisms. In this study, we investigated the role of AMPK on autophagy regulation in HCN cells following insulin-withdrawal. Genetic and pharmacological activation of AMPK promoted ACD, while inhibition of AMPK yielded the opposite outcomes. These data suggest that AMPK can be a positive regulator of ACD in HCN cells following insulin withdrawal. β 2016 DGIST1. Introduction 1 --
2. Materials and methods 5 --
2.1 Cell culture 5 --
2.2 Antibodies and reagents 5 --
2.3 Cell death assay 5 --
2.4 GFP-LC3 puncta assay 6 --
2.5 Western blot 6 --
2.6 Transfection 6 --
2.7 Sh-RNA Lentiviral system 7 --
2.8 Statistical analysis 7 --
3. Results 8 --
3.1 AMPK activator, A769662 increased cell death following insulin withdrawal. 8 --
3.2 Ectopic expression of AMPK constructs modulated cell death. 8 --
3.3 Silencing of AMPK reduced ACD in insulin-deprived HCN cells. 9 --
3.4 Cell death mode induced by genetic and pharmacological activation of AMPK was ACD, not apoptosis. 9 --
3.5 Suppression of autophagy related gene, Atg7 prevented ACD. 10 --
4. Discussion 11 --
5. Figure legends 13 --
6. Figures 16 --
Reference 24 --
Abstract in Korean 26--μ₯μ 100μΈ μλμ μ΄λ₯΄λ©° ν΄νμ± λμ§ν νμκ° μ¦κ°νκ³ μμΌλ©°, λλ ·ν μΉλ£λ°©λ²μ΄ μμ΄μ μ¦κ°νλ νμμ λν ν΄κ²°λ°©μμ΄ μ λλ‘ λ§λ ¨λμ§ μλ κ²μ΄ μ¬νμ λ¬Έμ λ‘ λλλκ³ μλ€. λνμ ν΄νμ± λμ§νμΈ μμ―νμ΄λ¨Έ μΉλ§€λ νν¨μ¨λ³κ³Ό κ°μ μ§λ³λ€μ μ κ²½μΈν¬λ€μ΄ μ£½μ΄μ μκ° μ λμ μΌλ‘ μ€μ΄λλ μ¦μμ 보μΈλ€. μκ°ν¬μνμμ ν¬μ λ₯μ λͺΈ μμμ λμ¬μ°λ¬Όλ‘ λ°μν λͺΈμ νμμΉ μλ λ¬Όμ§λ€μ μμ κΈ° μν λ°©λ²μΌλ‘ μΈν¬ λ΄ μκΈ°νμμ±μ κΈ°μ¬λ₯Ό νλ μμ£Ό μ€μν κ³Όμ μ΄λ€. κ·Έλ¬λ μ΄λ€ μ΄μ λ‘ μΈν΄ μ²΄λ΄ μκ°ν¬μνμμ΄ μ μμ μΌλ‘ μΌμ΄λμ§ μμΌλ©΄, λ§μ μ§λ³ νΉνλ ν΄νμ± λμ§νμ μΌκΈ°νλ€λ μ°κ΅¬λ€μ΄ λ§μ΄ μ§νλμλ€. νμ§λ§ μ€μλμ λΉν΄ μ νν μκ°ν¬μνμ, κΆκ·Ήμ μΌλ‘ μΈν¬μ¬λ©Έ κΈ°μ μ λν μ΄ν΄κ° λΆμ‘±ν΄ λ λ§μ μ°κ΅¬κ° μ΄λ£¨μ΄μ ΈμΌ νλ€κ³ λ³΄κ³ μλ€.
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νμλ€. λ λμκ° μ΄ μ°κ΅¬λ μΆ©λΆνμ§ λͺ»ν μκ°ν¬μνμμΌλ‘ μΈν΄ μΌμ΄λλ ν΄νμ± λμ§ν λλ λΆνμνκ² κ³Όνμ±ν λ λ μΈν¬μμμ μκ°ν¬μνμμ μ‘°μ νκΈ° μν΄, AMPK μ΄μ§μ λλ μ΅μ μ λ₯Ό μ¬μ©νλ€λ©΄ μΉλ£μ λ‘λ μΆ©λΆν μ¬μ©ν μ μμ κ²μ΄λΌλ κ°λ₯μ±μ 보μ¬μ£Όκ³ μλ€. β 2016 DGISTMasterdCollectio
Distinct Signaling Pathways for Autophagy-Driven Cell Death and Survival in Adult Hippocampal Neural Stem Cells
autophagy; autophagic cell death; ERK; JNK; GSK-3Ξ²; adult hippocampal neural stem cellsAutophagy is a conserved cellular catabolic process responsible for degrading and recycling cellular materials and plays beneficial roles in maintaining cellular and organismal homeostasis by preventing the accumulation of toxic protein aggregates, removing damaged organelles, and providing bioenergetic substrates essential for survival. However, autophagy can also induce cell death depending on the cellular context, and the signaling pathways differentially regulating these opposite outcomes remain largely unknown.
Our previous study demonstrated that insulin withdrawal (IW) or corticosterone (CORT) induces autophagic cell death in adult hippocampal neural stem cells. In contrast, metabolic stresses caused by 2-deoxy-D-glucose (2DG) and glucose-low (GL) induce cytoprotective autophagy without cell death. By comparing these conditions, we revealed that distinct signaling pathways regulate cell death-inducing autophagy and survival-promoting autophagy, with ERK and JNK involved in the latter and GSK-3Ξ² in the former. Furthermore, our observations revealed mitochondrial dysfunction during death-inducing autophagy, whereas protective autophagy was associated with lipophagy. These findings suggest that autophagy regulates cell death and survival in HCN cells via distinct signaling pathways.|μκ°ν¬μμ μΈν¬ μμ¬λ₯Ό λΆν΄νκ³ μ¬νμ©νλ μΈν¬ λμ¬κ³Όμ μΌλ‘, λ
μ± λ¨λ°±μ§ν©μ²΄μ μΆμ λ°©μ§, μμλ μΈν¬κΈ°κ΄ μ κ±°, μμ‘΄μ νμμ μΈ μ체 μλμ§ κΈ°μ§ μ 곡 λ±μ μ΄μ μ΄ μλ€. κ·Έλ¬λ μ΄λ ν μ΄μ μμ, 쑰건μ λ°λΌ μκ°ν¬μνμμ μΈν¬ μ¬λ©Έ λλ 보νΈμ μΈ μν μ λ€λ₯΄κ² νλ κ²μ΄ κ΄μ°°λμλ€. λ°λλλ νμμ κ²°κ³Όλ₯Ό κ°κ° μ‘°μ νλ μ νΈμ λ¬ κ²½λ‘λ μμ§ μ μλ €μ Έ μμ§ μμλ€.
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(CORT)μ μν΄ μ±μΈ ν΄λ§ μ κ²½μ€κΈ°μΈν¬κ° μκ°ν¬μνμμ΄ μ¦κ°νλ©° μ£½λ κ²μ λ°κ²¬νλ€. μ΄ μ°κ΅¬μμλ μμ μ°κ΅¬μλ λ¬λ¦¬ 2-Deoxy-D-Glucose (2DG)μ μ μ ν¬λλΉ(GL) 쑰건μμλ μκ°ν¬μνμμλ μΈν¬κ° μ£½μ§ μμκ³ , μ€νλ € μκ°ν¬μνμμ΄ μΈν¬ 보νΈμ κΈ°μ¬νλ κ²μ λ°κ²¬νμλ€. μ°λ¦¬λ IW λ° CORT 쑰건과 2DG λ° GLμ²λ¦¬λ₯Ό λΉκ΅νμ¬, 보νΈμ μΈ-μκ°ν¬μμ μ λνλ μ νΈμ λ¬μ²΄κ³λ ERK λ° JNKκ° κ΄μ¬νλλ° λ°ν΄, μΈν¬μ¬λ©Έ-μκ°ν¬μμ μ‘°μ νλ μ νΈμ λ¬μ²΄κ³λ GSK-3Ξ²κ° κ΄μ¬νλ€λ κ²μ λ°νλλ€. λν, μ£½λ μκ°ν¬μνμμμλ λ―Έν μ½λ리μ κΈ°λ₯ μ΄μμ΄ λνλ¬μΌλ©°, 보νΈμ μΈ μκ°ν¬μνμμ μ§λ°© ν¬μ(Lipophagy)μ΄ κ΄λ ¨λμ΄ μλ κ²μ νμΈνμλ€. μ΄λ¬ν κ²°κ³Όλ μ±μΈ ν΄λ§ μ κ²½μ€κΈ°μΈν¬μμ μΈν¬μ¬λ©Έκ³Ό μμ‘΄ μ΄μ§ μκ°ν¬μνμμ΄ μλ‘ λ€λ₯Έ μ νΈμ λ¬ κ²½λ‘λ₯Ό ν΅ν΄ μ‘°μ λ μ μλ€λ κ²μ μμ¬νλ€.
λ³Έ μ°κ΅¬λ μκ°ν¬μ μ°κ΅¬λΆμΌμμ λ
Όλμ΄ λ§μ μκ°ν¬μνμμ μν , βμ£½μμ μΌκΈ°νλκ° νΉμ 보νΈμ μΈ μν₯μ λ―ΈμΉλκ°βμ λν μλ‘μ΄ λ¨μλ₯Ό μ 곡νλ€. μ§κΈκ» μ°λ¦¬κ° μλ μ°κ΅¬λ²μμμλ ν μΈν¬λ΄μμ λκ°μ§ λ€λ₯Έ μκ°ν¬μνμμ λ°μμ μ²μ λ³΄κ³ νλ μ°κ΅¬μ΄λ©° λ³Έ μ°κ΅¬λ₯Ό ν΅ν΄ λ€λ₯Έ μ νΈμ λ¬μ²΄κ³μ μν μ‘°μ μ΄ μκ°ν¬μμ μΈν¬μ¬λ©Έμ νΉμ μμ‘΄μ μ λνλλ° κ΄λ ¨μ΄ μκ³ , μ‘°μ λ μ μλ€λ κ°λ₯μ±μ μ μνλ€.β
. Introduction 1
1. Cell death mechanism 1
1.1 Apoptosis 3
1.2. Necrosis 3
1.3. Autophagy 4
2. Autophagy in adult hippocampal neural stem cells 9
2.1 Death-inducing autophagy 12
2.1.1 Mitochondria β ATP, Mitochondrial membrane potential, reactive oxygen stress 12
2.1.2 Glycolysis / Gluconeogenesis 14
2.1.3 GSK-3Ξ² 17
2.2 Protective autophagy 17
2.2.1 Lipid droplet, lipophagy 17
2.2.2 MAPK 20
3. Aim/hypothesis/significance of this study 21
β
‘. Materials and Methods 23
1. Materials 23
2. Cell cultures 23
3. Cell death assay 23
4. Generation of stable cell lines 24
5. Transfection 24
6. Confocal imaging 25
7. Western blotting 25
8. MitoSOX staining using fluorescence-activated cell sorting (FACS) analysis 25
9. ATP measurement assay 26
10. Quantitative real-time PCR 26
11. Statistical analysis 26
β
’. Results 28
Result 1. Autophagy is induced by four cellular stress conditions in HCN cells. 28
Result 2. 2DG and GL did not affect cell viability, whereas IW and CORT triggered autophagic cell death. 30
Result 3. 2DG-induced autophagy acted protectively and prevented IW- or CORT-induced cell death. 34
Result 4. MAPK inhibition prevents 2DG-induced autophagy but has no effect on IW- or CORT-induced autophagy. 38
Result 5. The blockade of ERK and JNK impedes the protective effects of 2DG. 38
Result 6. The inhibition of GSK-3Ξ² blocks IW- or CORT-induced ACD but not 2DG-induced autophagy. 44
Result 7. IW and CORT induce ATP depletion and mitochondrial ROS accumulation in HCN cells, unlike 2DG or GL treatment. 47
Result 8. Gluconeogenesis genes, but not glycolysis genes were up-regulated after ACD. 51
Result 9. Lipophagy is associated with MAPK-driven survival autophagy. 54
β
£. Discussion 59
References 62
Abstract in Korean 82DoctordCollectio
Distinct Signaling Pathways for Autophagy-Driven Cell Death and Survival in Adult Hippocampal Neural Stem Cells
Autophagy is a cellular catabolic process that degrades and recycles cellular materials. Autophagy is considered to be beneficial to the cell and organism by preventing the accumulation of toxic protein aggregates, removing damaged organelles, and providing bioenergetic substrates that are necessary for survival. However, autophagy can also cause cell death depending on cellular contexts. Yet, little is known about the signaling pathways that differentially regulate the opposite outcomes of autophagy. We have previously reported that insulin withdrawal (IW) or corticosterone (CORT) induces autophagic cell death (ACD) in adult hippocampal neural stem (HCN) cells. On the other hand, metabolic stresses caused by 2-deoxy-D-glucose (2DG) and glucose-low (GL) induce autophagy without death in HCN cells. Rather, we found that 2DG-induced autophagy was cytoprotective. By comparing IW and CORT conditions with 2DG treatment, we revealed that ERK and JNK are involved with 2DG-induced protective autophagy, whereas GSK-3Ξ² regulates death-inducing autophagy. These data suggest that cell death and survival-promoting autophagy undergo differential regulation with distinct signaling pathways in HCN cells. Β© 2023 by the authors.TRU
Flexible CFD meshing strategy for prediction of ship resistance and propulsion performance
Surface Electromyography-Driven Parameters for Representing Muscle Mass and Strength
The need for developing a simple and effective assessment tool for muscle mass has been increasing in a rapidly aging society. This study aimed to evaluate the feasibility of the surface electromyography (sEMG) parameters for estimating muscle mass. Overall, 212 healthy volunteers participated in this study. Maximal voluntary contraction (MVC) strength and root mean square (RMS) values of motor unit potentials from surface electrodes on each muscle (biceps brachii, triceps brachii, biceps femoris, rectus femoris) during isometric exercises of elbow flexion (EF), elbow extension (EE), knee flexion (KF), knee extension (KE) were acquired. New variables (MeanRMS, MaxRMS, and RatioRMS) were calculated from RMS values according to each exercise. Bioimpedance analysis (BIA) was performed to determine the segmental lean mass (SLM), segmental fat mass (SFM), and appendicular skeletal muscle mass (ASM). Muscle thicknesses were measured using ultrasonography (US). sEMG parameters showed positive correlations with MVC strength, SLM, ASM, and muscle thickness measured by US, but showed negative correlations with SFM. An equation was developed for ASM: ASM = β26.04 + 20.345 Γ Height + 0.178 Γ weight β 2.065 Γ (1, if female; 0, if male) + 0.327 Γ RatioRMS(KF) + 0.965 Γ MeanRMS(EE) (SEE = 1.167, adjusted R2 = 0.934). sEMG parameters in controlled conditions may represent overall muscle strength and muscle mass in healthy individuals
Flexible CFD meshing strategy for prediction of ship resistance and propulsion performance
p Long-Term Human Histologic Evaluation of Sinus Bone Augmentation and Simultaneous Implant Placement
This study aimed to histologically and histomorphometrically evaluate osseointegration following simultaneous implant placement and maxillary sinus augmentation. Three retrospective human cases are described in which implants were placed at the maxillary sinus site augmented with deproteinized bovine bone mineral (DBBM) and later retrieved due to implant fracture after 5 to 8 years of occlusal loading. The removed implants with bone were processed for histologic evaluation, and bone-to-implant contact (BIC), bone area (BA), and mirror-image bone area (MIBA) were measured. Mature lamella bone was mainly observed, and some unabsorbed grafted bone particles remained in all cases. The measured values of BIC, BA, and MIBA in the three consecutive threads with the highest values were 86.0% to 91.2%, 65.8% to 91.9%, and 73.0% to 90.4%, respectively, and there were no signs of inflammation. Within the limits of this study, these cases demonstrate successful bone formation after maxillary sinus bone augmentation with DBBM and simultaneous implant placement. Int J Periodontics Restorative Dent 2022;42:93-100. doi:N
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