Citation

Wan-Guang ZHANG, Li HE, Hua-Qing SU, Xue-Mei SHI, Bo ZHANG, Si-Si WU, Li MEI, Katirai FOAD, Yong-Jian XU, Zhen-Xiang ZHANG, Jian-Ping ZHAO, Wei-Ning XIONG, Guo-Hua ZHEN, Hui-Lan ZHANG. J. Huazhong Univ. Sci. Technolog. Med. Sci. 2014; (6): 337-42.

Copyright

(Copyright © 2014, Huazhong University of Science and Technology)

DOI

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PMID

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Abstract

Alveolar epithelial type II (AT II) cells are essential for lung development and remodeling, as they are precursors for type I cells and also produce other non-repair cells (fibroblasts). Progenitor cells are believed to possess capability of multi-potent transdifferentiation, which is closely related to the niche, suggesting the importance of establishment of a lung progenitor cell niche model. We hypothesized that pulmonary surfactant-associated protein A (SPA) suicide gene system would cause AT II cell to kill itself through apoptosis and leave its niche. In vitro, the recombinant adeno-associated virus vectors-SPA-thymidine kinase (rAAV-SPA-TK) system was established to get targeted apoptotic AT II cells. The apoptosis of AT II cells was detected by using MTT. The results showed that cloned SPA gene promoter had specific transcriptional activity in SPA high expression cells, and SPA high expression cells (H441) transfected with TK gene had higher sensitivity to ganciclovir (GCV) than SPA low expression cells (A549). In vivo, increased apoptosis of AT II cells induced by GCV in rAAV-SPA-TK system was observed by TUNEL. Finally, the successful packaging and application of rAAV-SPA-TK system provide experimental basis to get specific lung progenitor cell (AT II) niche in vitro and in vivo.

Language: en