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治疗性高碳酸血症对大鼠移植肺中 γδT 细胞表达和功能的影响。

Effects of therapeutic hypercapnia on the expression and function of γδT cells in transplanted lungs in rats.

机构信息

Department of Anesthesia, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Department of Anesthesia, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

出版信息

Immun Inflamm Dis. 2024 Mar;12(3):e1220. doi: 10.1002/iid3.1220.

DOI:10.1002/iid3.1220
PMID:38506409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10953205/
Abstract

OBJECTIVE

To investigate the effect of therapeutic hypercapnia on the expression and function of gamma delta T (γδ T) cells during ischemia-reperfusion injury (IRI) after lung transplantation.

METHODS

We randomly divided male Wistar rats into three groups (n = 6 in each group), the control group (group N), the IRI group (group I), and the therapeutic hypercapnia group (group H). We then assessed pulmonary edema, neutrophil infiltration, wet-to-dry (W/D) weight ratio, and microscopic histopathology and separately measured the levels of γδT cell surface antigen (TCR) and Interleukin-17 (IL-17) using flow cytometry and enzyme-linked immunosorbent assays (ELISAs).

RESULTS

The infiltration of neutrophils and the expression of TCR and IL-17 were significantly increased in the I group compared to the control, and the biopsy edema in group I was more severe. Arterial partial pressure of oxygen (PaO2) was decreased after reperfusion in group I compared with the control group. W/D weight ratio, neutrophil infiltration, and the expression of TCR and IL-17 decreased drastically in the H group compared to the I group.

CONCLUSION

Our findings suggest that γδ T lymphocytes were directly involved in lung injury. In addition, therapeutic hypercapnia effectively reduced the expression of γδ T cells and IL-17, and this has the potential to become a treatment strategy for IRI and an intervention to improve lung function.

摘要

目的

探讨治疗性高碳酸血症对肺移植后缺血再灌注损伤(IRI)期间γδ T(γδ T)细胞表达和功能的影响。

方法

我们将雄性 Wistar 大鼠随机分为三组(每组 6 只),分别为对照组(N 组)、IRI 组(I 组)和治疗性高碳酸血症组(H 组)。然后评估肺水肿、中性粒细胞浸润、湿干重(W/D)比和显微镜组织病理学,并分别使用流式细胞术和酶联免疫吸附试验(ELISA)测量γδ T 细胞表面抗原(TCR)和白细胞介素 17(IL-17)的水平。

结果

与对照组相比,I 组的中性粒细胞浸润和 TCR 和 IL-17 的表达显著增加,且 I 组的活检水肿更严重。与对照组相比,I 组再灌注后动脉血氧分压(PaO2)降低。与 I 组相比,H 组的 W/D 重量比、中性粒细胞浸润以及 TCR 和 IL-17 的表达明显降低。

结论

我们的研究结果表明,γδ T 淋巴细胞直接参与了肺损伤。此外,治疗性高碳酸血症可有效降低 γδ T 细胞和 IL-17 的表达,这可能成为 IRI 的治疗策略,并改善肺功能的干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/2bc581c064f2/IID3-12-e1220-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/41c8529c0381/IID3-12-e1220-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/126a9e2a72a6/IID3-12-e1220-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/8b41a90d206c/IID3-12-e1220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/186b4843962f/IID3-12-e1220-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/2bc581c064f2/IID3-12-e1220-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/41c8529c0381/IID3-12-e1220-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/126a9e2a72a6/IID3-12-e1220-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/8b41a90d206c/IID3-12-e1220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/186b4843962f/IID3-12-e1220-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b6/10953205/2bc581c064f2/IID3-12-e1220-g006.jpg

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