Ministry of Education

government📍 Dhaka, Bangladesh
2
Alpha-gal Syndrome Publications
42
Alpha-gal Syndrome Researchers

Publications

Comparative in vitro and in vivo assessment of three experimental extracellular matrix meshes for soft tissue remodeling.

Ruan W, Wang G, Qu Q, Gai X, Wang C, et al.
Scientific reports •

The development of standardized cross-species evaluation frameworks is urgently needed for absorbable extracellular matrix (ECM) meshes, due to significant variations in safety and efficacy across tissue sources. This study establishes a multi-dimensional assessment system to quantify material-specific bio-functional correlations. Three ECM meshes-human acellular dermis (HAD), porcine acellular dermis (PAD), and porcine small intestinal submucosa (SIS)-were systematically characterized using integrated in vitro and in vivo analyses. Assessments included physicochemical properties (e.g., degradation kinetics via collagenase digestion), immunogenic residues (α-Gal epitopes and DNA quantification), and biocompatibility. In vivo performance was evaluated using rabbit subcutaneous (for degradation and immune response) and rat abdominal defect models (for macrophage polarization: CD206⁺/CD86⁺ ratio and collagen deposition). HAD exhibited superior structural stability (82.3% ± 1.2% residual mass after 7-day collagenase digestion), whereas SIS degraded most rapidly (10.5% ± 0.42%; p < 0.01 vs PAD) but provoked severe foreign body reactions (2.3-fold higher vs HAD at 13 weeks, p = 0.017). Notably, HAD uniquely promoted sustained M2-dominant macrophage polarization (CD206⁺/CD86⁺ ratio = 2.1 vs SIS = 0.7), which reduced inflammation and enhanced collagen remodeling (p < 0.05 vs SIS). Serum metabolomic analysis indicated that ECM mesh implantation induced a reprogramming of host amino acid metabolism, marked by a notable acceleration in L-methionine metabolism. The proposed integrated evaluation framework successfully identifies material-specific correlations among degradation behavior, immune response, and metabolic regulation, providing critical benchmarks for the rational design of immunomodulatory ECM meshes.

[The role RNA interference of alpha1, 3GT plays in resistance to complement mediated cytotoxicity of porcine endothelial cells].

Zhu M, Xia ZX, Wang SS, Cao RH, Qi HG, et al.
Zhonghua yi xue za zhi •

To evaluate whether RNA interference can protect porcine endothelial cells from complement mediated cytotoxicity. Immortalized porcine aortic endothelial cells of the line PED were cultured and transfected with alpha1,3-galactosyltransferase (alpha1, 3-GT) specific siRNAs. Cells transfected with mismatch SiRNA was used as negative controls. Forty-eight hours later the cells were collected. The expression of alpha1, 3-GT mRNA was examined by RT-PCR. The expression of alpha-Gal was examined by flow cytometry. PED cells ere labeled with (51)Cr and mixed with normal human serum (NHS). The release of (51)Cr was measured by gamma-ray counter. Heat inactivated NHS (HINHS) was used as control. Two isoforms (isoform 1 and isoform 2) were amplified from the PED cells. The expression of alpha1, 3-GT in the PED cells transfected with SiRNA-1 was lower by 70% in comparison with the mock group (69% for the isoform 1 and 72% for the isoform 2, both P < 0.05). However, the expression of alpha1, 3-GT in the PED cells transfected with SiRNA21 was not different from those in the mock group and mismatch group (both P > 0.05). Flow cytometry showed that the average fluorescence intensity of the PED cells transfected with SiRNA-1 was 52, 9, significantly lower than that of the mismatch group and mock group (493.9 and 5-5.7 respectively, both P < 0.0). Fluorescence microscopy observed the "silence effect" of alphaGal after SiRNA-1 transfection. Added with 20% and 40% NHS, the cell dissolution rate of the SiRNA transfection group was lower than that of the mock group by 70% and 60% respectively. alpha1, 3GT gene silencing actually occurs following transfection of SiRNA-1. Porcine endothelial cells can be the targets of RNAi.