Publications by authors named "Yindi Wu"

Host remodeling of decellularized extracellular matrix (dECM) material through the appropriate involvement of immune cells is essential for achieving functional organ/tissue regeneration. As many studies have focused on the role of macrophages, only few have evaluated the role of regulatory T cells (Tregs) in dECM remodeling. In this study, we used a mouse model of traumatic muscle injury to determine the role of Tregs in the constructive remodeling of vascular-derived dECM.

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  • Embryoid bodies (EB) are affected by culture conditions, and this study investigates PEG 300's role in EB formation and differentiation.
  • Adding PEG 300 improves the efficiency of EB formation and enhances differentiation towards mesoderm, marked by increased T/Bry expression and decreased TUBB3.
  • PEG-pretreated EBs show superior differentiation into vascular smooth muscle cells (VSMCs), exhibiting higher expression of markers and improved function, emphasizing the significance of PEG 300 in promoting mesodermal gene expression and cellular differentiation.
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  • - The study focuses on vascular smooth muscle cells (VSMCs) and aims to improve their use in tissue-engineered vascular constructions by utilizing a three-dimensional culture system.
  • - Researchers treated calf VSMCs with tumor necrosis factor-alpha (TNF-α) before culturing them in different settings, and then assessed their characteristics using various scientific methods.
  • - Results showed that TNF-α caused VSMCs to switch from a contractile to a synthetic phenotype, significantly enhancing their proliferation and migration abilities in both two-dimensional and three-dimensional cultures.
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Background: The contractile phenotype of vascular smooth muscle cells (VSMCs) results in good diastolic and contractile capacities, and its altered function is the main pathophysiological basis for diseases such as hypertension. VSMCs exist as a synthetic phenotype in vitro, making it challenging to maintain a contractile phenotype for research. It is widely recognized that the common medium in vitro is significantly less crowded than in the in vivo environment.

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To create tissue-engineered vascular grafts (TEVGs) in vitro, vascular smooth muscle cells (VSMCs) must function effectively and produce sufficient extracellular matrix (ECM) in a three-dimensional space. In this study, we investigated whether the addition of insulin-transferrin-selenium (ITS), a medium supplement, could enhance TEVG formation. PGA fabric was used as the scaffold, and 1% ITS was added to the medium.

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  • Successful culture of small-diameter tissue-engineered vascular grafts (TEVGs) is hindered by low biomolecule deposition in traditional media, leading to inefficiencies in cell growth and tissue formation.
  • The study introduces macromolecular crowding (MMC) using carrageenan to enhance biomolecule deposition without harming cell health, resulting in increased collagen and fibronectin in cultured cells.
  • MMC significantly improves protein matrix structure formation in 3D cultures, which may address current limitations in tissue-engineered graft development for cardiovascular treatments.
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Background: The adhesion and survival state of cells on scaffold material is a major problem in tissue-engineered blood vessel (TEBV) culture. Platelet-rich plasma (PRP) contains a large amount of biologically active factors and fibrin, which is expected to play an important role in TEBV culture.

Purpose: To combine PRP with cells and scaffold material to promote cell adhesion and biological activity on the scaffold material.

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Gastric cancer (GC) is one of the most common malignancies in digestive system. Accumulating evidence reveals the critical role of long noncoding RNAs (lncRNAs) in GC development. The study aimed to explore the functions and mechanism of lncRNA actin alpha 2, smooth muscle antisense RNA 1 (ACTA2-AS1) in GC.

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Cesarean section results in scarring, which usually leads to adhesion between the subcutaneous fat and the abdominal wall muscle. The present study aimed to evaluate the therapeutic effect of autologous fat grafting on scar adhesion to the abdominal wall after cesarean section. Thirty-six patients with scar adhesion to the abdominal wall after cesarean section were recruited and treated between October 2013 and December 2015.

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Adipose-derived stem cells (ADSCs) have been documented as possible candidates for skin rejuvenation. However, the effects of ADSC-derived exosomes on photoaged skin remain to be fully elucidated. This study was aimed at determining the antiaging effects of ADSC-derived exosomes on photoaged skin.

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The objective of the present study was to investigate the application of a carbon arc lamp on wound healing in a rat cutaneous full-thickness wound model. In clinical practice, wound healing has been promoted by irradiation with a carbon arc lamp. However, the corresponding mechanism has not been clearly defined.

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Adipose‑derived stem cells (ADSCs) are mesenchymal stem cells that are often used in regenerative medicine. Maintaining ADSC viability is important, as this optimizes the curative effects of cell therapy. However, the optimal conditions for cell viability preservation remain unknown.

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Background: Recent evidence suggests that angiotensin II (Ang II) plays a role in cutaneous wound healing. Mesenchymal stem cells (MSCs) are known as a rich source of cells that re-establish healed skin. However, the potential impact of Ang II on MSC differentiation into keratinocytes is still unknown.

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Objective: The objective of the present study was to investigate the application of a carbon arc lamp on wound healing in a rat cutaneous full-thickness wound model.

Background Data: In clinical practice, wound healing has been promoted by irradiation with a carbon arc lamp. However, the corresponding mechanism has not been clearly defined.

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