Publications by authors named "Rongqing Pang"

Aims: Magnesium ions (Mg) play an important role in promoting cartilage repair in cartilage lesions. However, no research has focused on the role of Mg combined with microfracture (MFX) in hyaline-like cartilage repair mediated by cartilage injury. This study aimed to investigate the beneficial effects of the combination of MFX and Mg in cartilage repair.

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Previous studies have confirmed that burns and scalds can lead to metabolic disorders in the liver. However, the effects of severe burns at various time points on liver lipid metabolism disorders, as well as the relationship between these disorders and liver function, metabolism, and infection, have not yet been investigated.This study established a SD rat scald model, macroscopic observation of weight changes, histological staining, Western blot detection of fat browning and metabolic indicators, reverse transcription quantitative polymerase chain reaction analysis of the expression of liver new fat generation genes, determination of liver function and inflammatory indicators.

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Background: RAB42 (Ras-related protein 42) is a new small GTPase that controls the vesicular trafficking from endosomes to trans-Golgi network in mammalian cells. However, the role of RAB42 in multiple cancers, especially in liver hepatocellular carcinoma (LIHC), has not been well investigated.

Methods: A variety of cancer-related databases and online tools, including TCGA, GTEx, TARGET, QUANTISEQ, EPIC, RNAactDrug, CTR-DB, TIMER algorithms and Sangerbox, were applied to explore the correlation of RAB42 expression with prognosis, immune microenvironment, immune regulatory network, RNA modification, pathway activation and drug sensitivity in pan-cancer.

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Introduction: Ovarian Cancer (OC) is a heterogeneous malignancy with poor outcomes. Oxidative stress plays a crucial role in developing drug resistance. However, the relationships between Oxidative Stress-related Genes (OSRGs) and the prognosis of platinum-resistant OC remain unclear.

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The current first-line treatment for repairing cartilage defects in clinical practice is the creation of microfractures (MF) to stimulate the release of mesenchymal stem cells (MSCs); however, this method has many limitations. Recent studies have found that MSC-derived extracellular vesicles (MSC-EVs) play an important role in tissue regeneration. This study aimed to verify whether MSC-EVs promote cartilage damage repair mediated by MFs and to explore the repair mechanisms.

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Previous studies have confirmed that ascorbic acid (AA) can promote cartilage repair and improve cartilage differentiation in bone marrow mesenchymal stem cells. However, the use of microfracture (MFX) combined with AA to repair cartilage damage has not been studied. This study established a rabbit animal model and treated cartilage injury with different concentrations of AA combined with MFX.

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Background: The tumorigenesis of infused umbilical cord mesenchymal stem cells (UC-MSCs) is being preclinically evaluated.

Methods: We observed tumor formation in NOD SCID mice after a single subcutaneous injection of hUC-MSCs and the effect of these cells on tumor growth in tumor-bearing mice. Three generations (P5, P7, and P10) of hUC-MSCs (1 × 10) from two donors (hUC-MSC1 and hUC-MSC2) were inoculated subcutaneously into NOD SCID mice.

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Article Synopsis
  • The study investigates the effects of mouse umbilical cord mesenchymal stem cells (mUCMSCs) on the reproductive health of ageing C57 mice, focusing on their potential to repair ovarian function.
  • Aging mice with diminished ovarian function received mUCMSC injections, resulting in increased ovarian size, the presence of follicles, and enhanced hormone levels compared to a control group.
  • The findings indicate that mUCMSCs can reduce cell apoptosis and oxidative stress in granulosa cells by altering specific gene expressions and activating key cellular pathways, suggesting a potential for regenerative therapies in reproductive health.
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Based on the characteristics of modern weapon injury, a repetitive model of traumatic systemic inflammatory response syndrome (SIRS) and an evaluation system were established. The models were treated with GFP-labeled tree shrew umbilical cord mesenchymal stem cells (UCMSCs). Forty out of 50 tree shrews were used to make a unilateral femoral comminuted fracture.

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  • Ischemia-reperfusion injury significantly contributes to acute kidney injury and affects recovery after kidney transplants; this study explores the potential protective role of stem cell transplantation in such injuries.
  • The experiment involved 40 rabbits divided into four groups, with 30 establishing the injury model, and 10 serving as untreated controls; comparisons were made based on treatments with either induced or non-induced peripheral blood mononuclear cells (PBMCs).
  • Results showed that rabbits treated with induced PBMCs exhibited improved renal function and less severe pathological changes, indicating the therapeutic potential of these induced stem cells in mitigating kidney injury.
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  • A mouse model for allergic rhinitis (AR) was developed using BALB/c mice to aid in future research on the condition.
  • * The study involved preparing human umbilical cord mesenchymal stem cells (hUCMSCs), which were shown to be effective for tracking in animal studies and possibly for AR treatment.
  • * The transplantation of hUCMSCs, particularly through tail vein injection, demonstrated positive effects on the AR model, with a significant presence of these cells in the nasal area after two weeks.
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  • The study aimed to investigate how allogeneic umbilical cord mesenchymal stem cell (mUCMSC) transplantation affects the thymus in aging mice, potentially offering a new treatment for age-related thymic atrophy.
  • Results indicated that mUCMSC treatment improved thymus structure and function by analyzing changes in thymic tissue and immune cell markers, as well as promoting hair regeneration in the mice.
  • The findings suggest that mUCMSCs can reduce thymus aging by affecting specific senescence-related genes, though further research is needed to fully understand the underlying mechanisms.
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  • Inflammatory bowel disease (IBD) causes chronic inflammation in the gastrointestinal tract, and researchers are exploring new treatments with minimal side effects.
  • Mouse models of IBD were created using a solution called DSS, allowing scientists to test the effects of umbilical cord mesenchymal stem cells (UCMSCs) from both mice and humans.
  • The study found that UCMSCs improve survival rates and promote healing by enhancing key proteins in the intestines, offering a promising avenue for future IBD therapies.
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  • - The study explored the link between bone marrow mesenchymal stem cells (BMSCs) and aging by establishing an aging macaque model, analyzing how BMSCs from young and aged macaques differ in their characteristics.
  • - Researchers found that aging BMSCs showed decreased levels of key genes associated with aging, such as TERT, SIRT1, and SIRT6, using techniques like RT-PCR and Western blot.
  • - The team compared the effects of young and aged BMSCs on 293T cells, investigated secreted cytokines, and analyzed transcriptomes of peripheral blood mononuclear cells from macaques to understand gene transcription and regulatory mechanisms related to aging.
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  • Umbilical cord mesenchymal stem cells (UC-MSCs) demonstrate strong potential to improve survival and mitigate damage from acute radiation injury in tree shrews.
  • The treatment resulted in significant reductions in lung inflammation, apoptosis, and fibrosis, alongside enhanced blood counts and hematopoiesis.
  • Analysis indicated increased levels of anti-inflammatory cytokines and growth factors in treated animals, while inflammatory and fibrosis-related factors decreased, suggesting UC-MSCs could be a promising therapy for radiation injuries.
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  • This study evaluates the safety and immunological effects of umbilical cord mesenchymal stem cells from cynomolgus monkeys (mUC-MSCs) to guide human clinical applications.
  • Eighteen cynomolgus monkeys were split into three groups to assess the impact of different dosages, with observations made for any toxic reactions after repeated cell administrations.
  • Results showed no deaths or serious health issues, with some minor changes in certain blood levels that normalized after 28 days, suggesting a safe dosage for potential human use is significantly higher than current clinical amounts.
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  • Researchers are exploring a novel cell transplantation method using reprogrammed peripheral blood mononuclear cells (PBMCs) turned into induced mesenchymal stem cells (iMSCs) for treating chronic renal insufficiency.
  • An animal model of chronic renal insufficiency, created through unilateral ureteral obstruction, was used to evaluate the effectiveness of these iMSCs compared to non-induced PBMCs.
  • The study aims to assess the therapeutic potential of iMSC transplantation in managing chronic renal issues, hoping to provide new treatment options.
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  • * This study explored the use of islet-like cells from umbilical cord mesenchymal stem cells (UC-MSCs) in tree shrews with type 2 diabetes, showing effectiveness in reducing disease severity.
  • * UC-MSCs were found to differentiate into functional insulin-secreting cells through stimulation from high glucose and activation of Notch signaling, making this method a potentially simple and cost-effective diabetes treatment.
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Background: Endothelial progenitor cell (EPC) has significant age-dependent alterations in properties, but the role of Jagged1 in aging-induced decline of EPC functions remains unclear.

Methods: 2- and 20-month old healthy male Sprague-Dawley rats were used in present study. Jagged1 gene transfection was performed in EPC isolated from aged (AEPC) and young rats (YEPC), respectively.

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Hindlimb ischemia is still a clinical problem with high morbidity and mortality. Patients suffer from consequent rest pain, ulcers, cool limbs, and even amputation. Angiogenesis is a promising target for the treatment of ischemic limbs, providing extra blood for the ischemic region.

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Background: The establishment of a tree shrew model for systemic lupus erythematosus (SLE) provides a new method to evaluate the pathogenesis of autoimmune diseases.

Methods: Eighty tree shrews were randomly divided into four groups receiving either an intraperitoneal injection of pristane, lipopolysaccharide (LPS), or pristane and LPS, or no injection. Three weeks after injection, the SLE model tree shrews were divided into the model group and the treatment group.

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Objective: To explore the diagnostic value of serum C-X-C chemokine ligand 16 (CXCL16) in subjects with diabetic coronary artery disease (T2DM-CAD).

Methods: One hundred twenty Chinese subjects, including patients with coronary artery disease (CAD group), diabetic coronary artery disease (T2DM-CAD group), type 2 diabetes mellitus (T2DM group), and healthy controls of similar age and gender (control group), were enrolled in this study. Serum CXCL16 was detected by a sandwich-type enzyme linked immunosorbent assay (ELISA).

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The dysfunction of endothelial progenitor cells (EPCs) was found to be associated with vascular complications in diabetes mellitus (DM) patients. Previous studies found that regular exercise could improve the function of EPCs in DM patients, but the underling mechanism was unclear. Irisin, a newly identified myokine, was induced by exercise and has been demonstrated to mediate some of the positive effects of exercise.

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The aim of this study was to establish a tree shrew metabolic syndrome model and demonstrate the utility of MSCs in treating metabolic syndrome. We used tree shrew umbilical cord mesenchymal stem cell (TS-UC-MSC) transplantation for the treatment of metabolic syndrome to demonstrate the clinical application of these stem cells and to provide a theoretical basis and reference methods for this treatment. Tree shrew metabolic syndrome model showed significant insulin resistance, high blood sugar, lipid metabolism disorders, and hypertension, consistent with the diagnostic criteria.

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