相关实验视频

Updated: Jun 6, 2025

P. aeruginosa Infected 3D Co-Culture of Bronchial Epithelial Cells and Macrophages at Air-Liquid Interface for Preclinical Evaluation of Anti-Infectives
10:26

P. aeruginosa Infected 3D Co-Culture of Bronchial Epithelial Cells and Macrophages at Air-Liquid Interface for Preclinical Evaluation of Anti-Infectives

Published on: June 15, 2020

10.7K

人类CFTR缺陷的iPSC巨细胞在感染Pseudomonas aeruginosa时显示功能和转录基因反应受损

Claudio Rodriguez Gonzalez1, Débora Basílio-Queirós1, Anna-Lena Neehus2,3,4,5,6

  • 1Department of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.

Frontiers in immunology
|November 28, 2024
PubMed
概括

囊性纤维化巨细胞表现出细菌清除受损和炎症增加. 这项研究引入了一种新的人类诱导的多能干细胞衍生巨细胞模型,用于调查CFTR.

关键词:
伪omonas空气菌 伪omonas空气菌囊性纤维化症是什么这就是 iPSC 的意义.感染的感染感染.肺部免疫力 肺部免疫力巨细胞是什么?巨细胞是什么?

更多相关视频

Production and Characterization of Human Macrophages from Pluripotent Stem Cells08:05

Production and Characterization of Human Macrophages from Pluripotent Stem Cells

Published on: April 16, 2020

16.5K
Establishment of an In vitro System to Study Intracellular Behavior of Candida glabrata in Human THP-1 Macrophages13:47

Establishment of an In vitro System to Study Intracellular Behavior of Candida glabrata in Human THP-1 Macrophages

Published on: December 10, 2013

11.6K

相关概念视频

Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
192