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用于小鼠双光子脑成像的基于抗体的白细胞标记物。

Antibody-based leukocyte label for two-photon brain imaging in mice.

作者信息

Faulhaber Lila D, D'Costa Olivia, Shih Andy Y, Gust Juliane

机构信息

Center for Developmental Biology and Regenerative Medicine, Seattle, Washington, United States.

Seattle Children's Research Institute, Center for Integrative Brain Research, Seattle, Washington, United States.

出版信息

Neurophotonics. 2022 Jul;9(3):031917. doi: 10.1117/1.NPh.9.3.031917. Epub 2022 May 24.

DOI:10.1117/1.NPh.9.3.031917
PMID:35637871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9128835/
Abstract

To study leukocyte-endothelial interactions in a living system, robust and specific leukocyte labeling techniques are needed for two-photon microscopy of the cerebral microvasculature. We tested fluorophore-conjugated anti-CD45.2 monoclonal antibodies (mAb) to optimize dosing and two-photon imaging parameters for leukocyte labeling in healthy mice and a venous microstroke model. We retro-orbitally injected anti-CD45.2 mAb at 0.04, 0.4, and into BALB/c mice and used flow cytometry to analyze antibody saturation. Leukocyte labeling in the cortical microvasculature was examined by two-photon imaging. We also tested the application of CD45.2 mAb in a pathological leukocyte-endothelial adhesion model by photothrombotically occluding cortical penetrating venules. We found that of anti-CD45.2 antibody intravenously was sufficient to label 95% of circulating leukocytes. There was no depletion of circulating leukocytes after 24 h at the dosages tested. Labeled leukocytes could be observed as deep as from the cortical surface. The antibody reliably labeled rolling, crawling, and adherent leukocytes in venules around the stroke-affected tissues. We show that the anti-CD45.2 mAb is a robust reagent for acute labeling of leukocytes during two-photon microscopy of the cortical microvasculature.

摘要

为了在活体系统中研究白细胞与内皮细胞的相互作用,需要强大且特异的白细胞标记技术用于脑微血管的双光子显微镜检查。我们测试了荧光团偶联的抗CD45.2单克隆抗体(mAb),以优化健康小鼠和静脉微中风模型中白细胞标记的剂量和双光子成像参数。我们以0.04、0.4的剂量向BALB/c小鼠眶后注射抗CD45.2 mAb,并使用流式细胞术分析抗体饱和度。通过双光子成像检查皮质微血管中的白细胞标记情况。我们还通过光血栓闭塞皮质穿透小静脉,测试了CD45.2 mAb在病理性白细胞与内皮细胞黏附模型中的应用。我们发现静脉注射0.4 mg的抗CD45.2抗体足以标记95%的循环白细胞。在所测试的剂量下,24小时后循环白细胞没有减少。在距皮质表面深达150 μm处可以观察到标记的白细胞。该抗体可靠地标记了中风影响组织周围小静脉中滚动、爬行和黏附的白细胞。我们表明,抗CD45.2 mAb是皮质微血管双光子显微镜检查期间急性标记白细胞的一种强大试剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/9128835/baa18efb080c/NPh-009-031917-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/9128835/d34f2db53ceb/NPh-009-031917-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/9128835/62ee086abbc5/NPh-009-031917-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/9128835/30f62e91932d/NPh-009-031917-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/9128835/baa18efb080c/NPh-009-031917-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/9128835/d34f2db53ceb/NPh-009-031917-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/9128835/62ee086abbc5/NPh-009-031917-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/9128835/30f62e91932d/NPh-009-031917-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a35/9128835/baa18efb080c/NPh-009-031917-g004.jpg

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