Publications by authors named "Xi-Qiao Wang"

Hypertrophic scarring is a challenging issue for patients and clinicians. The prevalence of hypertrophic scarring can be up to 70% after burns, and patients suffer from pain, itching, and loss of joint mobility. To date, the exact mechanisms underlying hypertrophic scar formation are unclear, and clinical options remain limited.

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Most microvessels have been shown to become stenosed or completely occluded during hypertrophic scar progression. Here, we examined the morphology of capillary endothelial cells (ECs) and fibroblasts using immunofluorescence staining for CD31 and alpha-smooth muscle actin (α-SMA) and electron microscopy. In addition, ECs and fibroblasts were isolated from scar tissues, and the levels of transforming growth factor beta 1 (TGF-β1), platelet-derived growth factor (PDGF), endothelin 1 (ET-1), vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) were assayed using ELISAs.

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Article Synopsis
  • This study investigates how severe hypoxia (low oxygen) and malnutrition in scar tissue affect the regression of hypertrophic scars.
  • Fibroblasts from scars were subjected to different conditions (moderate/severe hypoxia and varying nutritional levels) to compare their effects on scar health.
  • The findings showed that severe hypoxia and malnutrition decreased cell viability and collagen production, leading to increased cell death and contributing to scar regression compared to normal conditions.
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The human hypertrophic scar undergoes hyperplasia and regression during progression. This study aimed to investigate whether fibroblasts in scar tissue undergo biological changes during the formation and regression of human hypertrophic scar. Using 32 scar samples, we measured collagen production by Masson's staining and the expression levels of transforming growth factor (TGF)-β1 and vascular endothelial growth factor (VEGF) by immunohistochemistry.

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Background: The skin color of human hypertrophic scar changes dynamically during scar progression.

Objective: To investigate whether hypoxia is dynamic during scar progression.

Methods: Thirty-five patients with early, proliferative, regressive, and mature scars were involved in this study.

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Extracellular matrix is one of the key environmental factors influencing cell survival and provides signals for cell morphological change, migration, proliferation and differentiation. However, the mechanism through which denatured collagen modulates the biological properties of fibroblasts, is unclear. We investigated the regulation of human fibroblast differentiation in vitro grown in collagen gels with different properties.

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This study aims to investigate the effect of Endostar injection on the rabbit ear hypertrophic scar formation and expand the use of Endostar. The rabbit ear hypertrophic scar models were established 4 weeks postoperation and were treated with Endostar injection; the control group was injected with saline, once a week, 3 times totally. At the seventh week, the scar tissue was harvested and processed with hematoxylin and eosin (HE) staining and CD34 immunohistochemistry and cell apoptosis assay.

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About 50% to 70% of all lower extremity amputations are related to diabetes infection. And antibiotic therapy is routinely used for all infected wounds to reduce the mortality of diabetic foot. Here, we report a case of diabetic foot with acute and deep severe infection.

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Hypertrophic scars and keloids are common problems after injury and cause functional and cosmetic deformities. A wide variety of treatments have been advocated for hypertrophic scars and keloids regression. Unfortunately, the reported efficacy has been variable.

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Objective: To explore the effect of focal-adhesion micromanipulation on the biological behavior of fibroblast.

Methods: Micro-pot was made by microcontact printing. The molecules of constitutive protein was adhered on micro-pot by self-assemble of peptides.

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Hypertrophic scars (HSc) have an excess of microvessels, most of which are partially or totally occluded. The mechanisms underlying microvessel endothelial cell accumulation and microvessel occlusion are poorly understood. In this study, we observed the microvessels with H&E staining and electron microscopy, and detected the cytokine expression with immunochemistry.

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Scars are a common complication of surgery or burn wound management. Scars occur over the body, affecting people of both sexes and all ages. Scar therapy is a constant clinical challenge; antimitotic drugs and radiotherapy are used with varying degrees of success.

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Article Synopsis
  • - Endothelial cells are suggested to play a significant role in the formation of scars, although the exact reasons for scar development are not fully understood.
  • - Researchers developed a new technique to isolate endothelial cells from hypertrophic scars by separating them from the surrounding tissue and other cell types.
  • - The isolated cells were confirmed to be endothelial in origin through their unique physical features and the expression of specific mRNA and proteins, making this method valuable for further research on endothelial cells in scar formation.*
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Article Synopsis
  • The study investigates the biological role of vascular endothelial cells in hypertrophic scars compared to normal skin tissue.
  • Histological examination revealed more capillary vessels in hypertrophic scars, which were smaller and more irregular in shape compared to normal skin.
  • The analysis showed that key growth factor levels (like TGF-beta1 and VEGF) in endothelial cells from hypertrophic scars were significantly lower than those found in normal skin, suggesting impaired function likely due to excessive collagen production and low oxygen levels in scar tissue.
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Article Synopsis
  • The degree of skin damage impacts how well wounds heal, and significant damage can lead to excessive scarring.
  • The dermis's three-dimensional structure acts as a guide for cell growth and affects how cells behave during the healing process.
  • Maintaining the integrity of the dermal tissue is essential for proper healing; damage to this structure can lead to abnormal tissue repair and scar formation.
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Objective: To investigate the influence of dermal template on the expressions of signal transduction protein Smad 3 and transforming growth factor beta1 and its receptor during wound healing process in patients with deep burns.

Methods: Twenty burn patients with excision of full thickness burn in the extremities were enrolled in the study and divided into two groups, i.e.

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Objective: To observe dynamically the influence of the application of dermal template on the p53 gene expression and apoptosis during wound repairing in burn patients.

Methods: Twenty burn patients were enrolled in the study and were divided into experiment (E, n = 11) and control (C, n = 9) groups. The escharectomy wounds in patients with 3rd degree burn in E group were covered with dermal template overlain with thin split-thickness autograft, while those in C group were covered with thin split-thickness autograft only.

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