Elewa Yaser Hosny Ali, Ichii Osamu, Mohamed Sherif Kh A, Kon Yasuhiro
Laboratory of Anatomy, Department of Basic Veterinary Sciences, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido 060-0818, Japan.
Department of Histology and Cytology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44511, Egypt.
Microsc Microanal. 2022 May 23:1-15. doi: 10.1017/S1431927622000654.
The purpose of this study is to elucidate the impact of bleomycin on the degree of lung injury and development of mediastinal fat-associated lymphoid clusters (MFALCs) in the lymphoproliferative mouse model (MRL/MpJ-Faslpr/lpr “Lpr”) and its control strain (MRL/MpJ “MpJ”). We analyzed immune cells, the degree of proliferation, lymphatic vessels (LVs), and high endothelial venules (HEVs) in lungs and MFALCs in Lpr and MpJ mice on the 7th and 21st days following intranasal instillation of either bleomycin (BLM group) or PBS (PBS group). The BLM group showed a significant increase in the size of MFALCs, lung injury score, and positive area ratios of LVs, HEVs, and immune cells (especially macrophages, B- and T-lymphocytes) on both days 7 and 21. Interestingly, the lungs in the BLM group on day 21 showed higher collagen deposition and cellular infiltration in MpJ and Lpr, respectively. Moreover, significant positive correlations were observed between the size of MFALCs and lung injury. In conclusion, BLM could exert lung fibrosis or lymphoproliferative infiltration in chronic stages in MpJ and Lpr, respectively, and this varied effect could be due to the variations in the degree of immune cell proliferation and the development of LVs and HEVs among the studied strains.
本研究的目的是阐明博来霉素对淋巴增殖性小鼠模型(MRL/MpJ-Faslpr/lpr“Lpr”)及其对照品系(MRL/MpJ“MpJ”)的肺损伤程度和纵隔脂肪相关淋巴簇(MFALCs)发育的影响。我们在经鼻滴注博来霉素(BLM组)或PBS(PBS组)后的第7天和第21天,分析了Lpr和MpJ小鼠肺组织和MFALCs中的免疫细胞、增殖程度、淋巴管(LVs)和高内皮微静脉(HEVs)。BLM组在第7天和第21天的MFALCs大小、肺损伤评分以及LVs、HEVs和免疫细胞(尤其是巨噬细胞、B淋巴细胞和T淋巴细胞)的阳性面积比均显著增加。有趣的是,第21天BLM组的肺组织在MpJ和Lpr小鼠中分别表现出更高的胶原沉积和细胞浸润。此外,MFALCs大小与肺损伤之间存在显著正相关。总之,博来霉素在慢性期可分别在MpJ和Lpr小鼠中导致肺纤维化或淋巴增殖性浸润,这种不同的效应可能是由于所研究品系中免疫细胞增殖程度以及LVs和HEVs发育的差异所致。