Protocol for fine casting, imaging, and analysis of murine vascular networks with VALID

Summary: The majority of fluorescent vessel labeling techniques currently available are limited by their expense, incomplete labeling, or complexity. Here, we present VALID (vessel labeling via gelatin-based lipophilic dye solution)—a protocol for complete labeling of different vascular networks. We...

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Main Authors: Jingtan Zhu, Xiaomei Liu, Jianyi Xu, Zhang Liu, Yating Deng, Junyao Dai, Tingting Yu, Dan Zhu
Format: Article
Language:English
Published: Elsevier 2023-09-01
Series:STAR Protocols
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666166723004082
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author Jingtan Zhu
Xiaomei Liu
Jianyi Xu
Zhang Liu
Yating Deng
Junyao Dai
Tingting Yu
Dan Zhu
author_facet Jingtan Zhu
Xiaomei Liu
Jianyi Xu
Zhang Liu
Yating Deng
Junyao Dai
Tingting Yu
Dan Zhu
author_sort Jingtan Zhu
collection DOAJ
description Summary: The majority of fluorescent vessel labeling techniques currently available are limited by their expense, incomplete labeling, or complexity. Here, we present VALID (vessel labeling via gelatin-based lipophilic dye solution)—a protocol for complete labeling of different vascular networks. We describe steps for preparing different dye hydrogels, murine vascular casting and tissue harvesting, immunolabeling, tissue clearing, and imaging, as well as detailed analysis of the vascular networks. This protocol is helpful for evaluating vascular lesions in studying different vessel-associated diseases.For complete details on the use and execution of this protocol, please refer to Zhu et al.1 : Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.
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spelling doaj.art-6e1afccdef924eae83645d59700a1d1a2023-08-07T04:04:57ZengElsevierSTAR Protocols2666-16672023-09-0143102441Protocol for fine casting, imaging, and analysis of murine vascular networks with VALIDJingtan Zhu0Xiaomei Liu1Jianyi Xu2Zhang Liu3Yating Deng4Junyao Dai5Tingting Yu6Dan Zhu7Britton Chance Center for Biomedical Photonics - MoE Key Laboratory for Biomedical Photonics, Advanced Biomedical Imaging Facility, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, 430074 Wuhan, Hubei, ChinaBritton Chance Center for Biomedical Photonics - MoE Key Laboratory for Biomedical Photonics, Advanced Biomedical Imaging Facility, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, 430074 Wuhan, Hubei, ChinaBritton Chance Center for Biomedical Photonics - MoE Key Laboratory for Biomedical Photonics, Advanced Biomedical Imaging Facility, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, 430074 Wuhan, Hubei, ChinaBritton Chance Center for Biomedical Photonics - MoE Key Laboratory for Biomedical Photonics, Advanced Biomedical Imaging Facility, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, 430074 Wuhan, Hubei, ChinaBritton Chance Center for Biomedical Photonics - MoE Key Laboratory for Biomedical Photonics, Advanced Biomedical Imaging Facility, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, 430074 Wuhan, Hubei, ChinaBritton Chance Center for Biomedical Photonics - MoE Key Laboratory for Biomedical Photonics, Advanced Biomedical Imaging Facility, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, 430074 Wuhan, Hubei, ChinaBritton Chance Center for Biomedical Photonics - MoE Key Laboratory for Biomedical Photonics, Advanced Biomedical Imaging Facility, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, 430074 Wuhan, Hubei, China; Corresponding authorBritton Chance Center for Biomedical Photonics - MoE Key Laboratory for Biomedical Photonics, Advanced Biomedical Imaging Facility, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, 430074 Wuhan, Hubei, China; Corresponding authorSummary: The majority of fluorescent vessel labeling techniques currently available are limited by their expense, incomplete labeling, or complexity. Here, we present VALID (vessel labeling via gelatin-based lipophilic dye solution)—a protocol for complete labeling of different vascular networks. We describe steps for preparing different dye hydrogels, murine vascular casting and tissue harvesting, immunolabeling, tissue clearing, and imaging, as well as detailed analysis of the vascular networks. This protocol is helpful for evaluating vascular lesions in studying different vessel-associated diseases.For complete details on the use and execution of this protocol, please refer to Zhu et al.1 : Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.http://www.sciencedirect.com/science/article/pii/S2666166723004082MicroscopyMolecular/Chemical ProbesBiotechnology and bioengineering
spellingShingle Jingtan Zhu
Xiaomei Liu
Jianyi Xu
Zhang Liu
Yating Deng
Junyao Dai
Tingting Yu
Dan Zhu
Protocol for fine casting, imaging, and analysis of murine vascular networks with VALID
STAR Protocols
Microscopy
Molecular/Chemical Probes
Biotechnology and bioengineering
title Protocol for fine casting, imaging, and analysis of murine vascular networks with VALID
title_full Protocol for fine casting, imaging, and analysis of murine vascular networks with VALID
title_fullStr Protocol for fine casting, imaging, and analysis of murine vascular networks with VALID
title_full_unstemmed Protocol for fine casting, imaging, and analysis of murine vascular networks with VALID
title_short Protocol for fine casting, imaging, and analysis of murine vascular networks with VALID
title_sort protocol for fine casting imaging and analysis of murine vascular networks with valid
topic Microscopy
Molecular/Chemical Probes
Biotechnology and bioengineering
url http://www.sciencedirect.com/science/article/pii/S2666166723004082
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