肺纤维化疾病模型

疾病简介

肺纤维化(pulmonary fibrosis,PF)是一种慢性进行性肺部疾病,会导致肺功能性气体交换功能受损、呼吸衰竭甚至死亡。该病的发生发展的起因是多种因素引起的早期肺部炎症,这些炎症的长期持续将导致肺内纤维组织沉积,诱发肺纤维化。已有研究表明,肺成纤维细胞的异常激活和分化是致病因素之一,而持续性肺泡损伤和修复不完全也可促进肺纤维化。

疾病模型

南模生物长期致力于自身免疫性疾病相关研究,开发了多种肺纤维化模型,均表现出良好的表型,为相关药物的药效评估和安全性评价提供了强有力的工具。

Bleomycin (BLM) is an anti‑cancer drug that has toxic side effects on the lungs. It induces DNA strand breaks and oxidative stress, thereby causing parenchymal inflammation, epithelial cell injury accompanied by reactive hyperplasia, epithelial‑mesenchymal transition, fibroblast activation and differentiation into myofibroblasts, as well as damage to the basement membrane and alveolar epithelium.

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Fig.1 Bleomycin induced pulmonary fibrosis in C57BL/6 (male, 10-12w) mice. (A) Body Weight. (B) Body Weight Change. (C) Survival Curve. 

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Fig2.Bleomycin induced pulmonary fibrosis in C57BL/6 (male, 10-12w) mice. (A) H&E and Masson stain. (B) Alveolar inflammation score. (C)Alveolar fibrosis score.

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