Jun Shu

ORCID: 0000-0003-0332-5620
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About
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Research Areas
  • Extracellular vesicles in disease
  • Electrospun Nanofibers in Biomedical Applications
  • Wound Healing and Treatments
  • Mesenchymal stem cell research
  • Tissue Engineering and Regenerative Medicine
  • Cancer-related molecular mechanisms research
  • Cardiac Fibrosis and Remodeling
  • Chronic Obstructive Pulmonary Disease (COPD) Research
  • Bone health and osteoporosis research
  • Cardiovascular Effects of Exercise
  • Kruppel-like factors research
  • Renal Transplantation Outcomes and Treatments
  • Metabolism and Genetic Disorders
  • Hip and Femur Fractures
  • MicroRNA in disease regulation
  • Ferroptosis and cancer prognosis

Chinese PLA General Hospital
2020-2024

Nanjing University of Chinese Medicine
2024

Kunming Medical University
2013-2021

Albert Einstein College of Medicine
2019

Guangdong General Hospital
2010

The inclusion of microRNAs (miRNAs) in extracellular microvesicles/exosomes (named cardiosomes when deriving from cardiomyocytes) allows their active transportation and ensures cell-cell communication. We hypothesize that cardiosomal miRNAs play a pivotal role the activation myofibroblasts following ischemic injury. Using murine model myocardial infarction (MI), we tested our hypothesis by measuring isolated fibroblasts expression levels set miRNAs, which are upregulated cardiomyocytes...

10.3390/ijms21010201 article EN International Journal of Molecular Sciences 2019-12-27

Biological scaffolds based stem cell delivery methods have emerged as a promising approach for tissue repair and regeneration. Here we developed hydrogel biological scaffold from human decellularized adipose matrix (hDAM) adipose-derived cells (hASCs) to accelerate chronic wound healing. The hDAM was prepared by pepsin mediated digestion pH controlled neutralization. morphology, survival, proliferation, angiogenic paracrine activity of hASCs cultured in the were assessed. Moreover,...

10.1002/jbm.a.37133 article EN Journal of Biomedical Materials Research Part A 2020-11-30

Our work aimed to investigate the interactive roles of transforming growth factor β1 (TGF-β1), ubiquitin-specific-processing protease 7 (USP7), and Yes-associated protein (YAP) in ferroptosis during sepsis-secondary acute lung injury (ALI). study demonstrated that was aggravated by TGF-β1 both cellular animal models injury. Additionally, YAP upregulated glutathione peroxidase 4 (GPX4) SLC7A11 regulating binding TEAD4 GPX4/SLC7A11 promoters. Furthermore, large tumor suppressor kinase 1...

10.1016/j.isci.2024.109667 article EN cc-by-nc-nd iScience 2024-04-05

Background: The inclusion of microRNAs (miRNAs) in extracellular microvesicles/exosomes (named cardiosomes when deriving from cardiomyocytes) allows their active transportation and ensures cell-cell communication. Aim: We hypothesize that cardiosomal miRNAs play a pivotal role the activation myofibroblasts following ischemic injury. Methods: Using bioinformatic approaches an established murine model myocardial infarction (MI, achieved via ligation left anterior descending coronary artery),...

10.1161/res.125.suppl_1.802 article EN Circulation Research 2019-08-02

Abstract Background Circulating microRNAs (miRNAs) are actively transported, via inclusion in extracellular microvesicles/exosomes (herein named cardiosomes since they deriving from cardiomyocytes), allowing protection degradation and underlying cell-cell communications. After myocardial infarction (MI), quiescent cardiac fibroblasts can acquire an activated phenotype, a recognized marker of such activation is the expression α-smooth muscle actin (α-SMA); cells commonly known as...

10.1093/eurheartj/ehz748.0913 article EN European Heart Journal 2019-10-01
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