Chunqing Hu

ORCID: 0009-0007-0839-3346
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About
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Research Areas
  • interferon and immune responses
  • Cytomegalovirus and herpesvirus research
  • Immune Cell Function and Interaction
  • Circular RNAs in diseases
  • MicroRNA in disease regulation
  • Cancer-related molecular mechanisms research
  • Hydrology and Watershed Management Studies
  • Regional Development and Environment
  • Inflammatory mediators and NSAID effects
  • Protease and Inhibitor Mechanisms
  • Osteoarthritis Treatment and Mechanisms
  • Environmental and Agricultural Sciences
  • Water Quality Monitoring and Analysis

Shaanxi Normal University
2024

Nanjing Drum Tower Hospital
2024

National Clinical Research Center for Digestive Diseases
2024

Nanjing University
2024

Tongji University
2014

Reactive astrocytes play critical roles in the occurrence of various neurological diseases such as multiple sclerosis. Activation is often accompanied by a glycolysis-dominant metabolic switch. However, role and molecular mechanism reprogramming activation have not been clarified. Here, we found that PKM2, rate-limiting enzyme glycolysis, displayed nuclear translocation EAE (experimental autoimmune encephalomyelitis) mice, an animal model Prevention PKM2 import DASA-58 significantly reduced...

10.7554/elife.98181.3 article EN cc-by eLife 2024-09-12

Reactive astrocytes play critical roles in the occurrence of various neurological diseases such as multiple sclerosis. Activation is often accompanied by a glycolysis-dominant metabolic switch. However, role and molecular mechanism reprogramming activation have not been clarified. Here, we found that PKM2, rate-limiting enzyme glycolysis, displayed nuclear translocation EAE (experimental autoimmune encephalomyelitis) mice, an animal model Prevention PKM2 import DASA-58 significantly reduced...

10.7554/elife.98181 article EN cc-by eLife 2024-06-14

Osteoarthritis (OA) is a highly incident total joint degenerative disease with cartilage degeneration as the primary pathogenesis. The matrix mainly composed of collagen, protein hallmark triple-helix structure, which unfolds collagen degradation on surface. A hybridizing peptide (CHP) synthetic that binds denatured triple helix, conferring potential disease-targeting possibility for early-stage OA. Here, we constructed an albumin nanoparticle (An) conjugated CHP, loaded...

10.1016/j.bioactmat.2024.08.004 article EN cc-by-nc-nd Bioactive Materials 2024-08-15

Abstract Reactive astrocytes play critical roles in the occurrence of various neurological diseases such as multiple sclerosis. Activation is often accompanied by a glycolysis-dominant metabolic switch. However, role and molecular mechanism reprogramming activation have not been clarified. Here, we found that PKM2, notoriously known rate-limiting enzyme glycolysis, displayed nuclear translocation EAE (experimental autoimmune encephalomyelitis) mice, an animal model Prevention PKM2 import...

10.1101/2024.04.22.590550 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2024-04-26

Reactive astrocytes play critical roles in the occurrence of various neurological diseases such as multiple sclerosis. Activation is often accompanied by a glycolysis-dominant metabolic switch. However, role and molecular mechanism reprogramming activation have not been clarified. Here, we found that PKM2, notoriously known rate-limiting enzyme glycolysis, displayed nuclear translocation EAE (experimental autoimmune encephalomyelitis) mice, an animal model Prevention PKM2 import DASA-58...

10.7554/elife.98181.1 preprint EN 2024-06-14

Reactive astrocytes play critical roles in the occurrence of various neurological diseases such as multiple sclerosis. Activation is often accompanied by a glycolysis-dominant metabolic switch. However, role and molecular mechanism reprogramming activation have not been clarified. Here, we found that PKM2, notoriously known rate-limiting enzyme glycolysis, displayed nuclear translocation EAE (experimental autoimmune encephalomyelitis) mice, an animal model Prevention PKM2 import DASA-58...

10.7554/elife.98181.2 preprint EN 2024-08-27
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