{"title":"Construction of Large Cranial Windows With Nanosheet and Light-Curable Resin for Long-term Two-Photon Imaging in Mice.","authors":"Taiga Takahashi, Yu Makino, Yosuke Okamura, Tomomi Nemoto","doi":"10.21769/BioProtoc.5373","DOIUrl":null,"url":null,"abstract":"<p><p>In vivo two-photon imaging of the mouse brain is essential for understanding brain function in relation to neural structure; however, its application is limited by the size and mechanical stability of conventional cranial windows. Here, we present the procedure of a large-scale cranial window technique based on the nanosheet incorporated into light-curable resin (NIRE) method. This approach utilizes a biocompatible polyethylene-oxide-coated CYTOP (PEO-CYTOP) nanosheet combined with light-curable resin, allowing the window to conform to the brain's curved surface. The protocol enables long-term, high-resolution, and multiscale imaging-from subcellular structures to large neuronal populations-in awake mice over several months. Key features • This protocol establishes large-scale cranial windows by combining a flexible, biocompatible PEO-CYTOP nanosheet with light-curable resin. • The large-scale cranial window provides long-term optical transparency and mechanical stability, enabling chronic in vivo imaging with minimal motion artifacts. • This approach facilitates multiscale two-photon imaging-from subcellular structures to large-scale neural networks-in awake mice.</p>","PeriodicalId":93907,"journal":{"name":"Bio-protocol","volume":"15 13","pages":"e5373"},"PeriodicalIF":1.0000,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12242551/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bio-protocol","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21769/BioProtoc.5373","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
In vivo two-photon imaging of the mouse brain is essential for understanding brain function in relation to neural structure; however, its application is limited by the size and mechanical stability of conventional cranial windows. Here, we present the procedure of a large-scale cranial window technique based on the nanosheet incorporated into light-curable resin (NIRE) method. This approach utilizes a biocompatible polyethylene-oxide-coated CYTOP (PEO-CYTOP) nanosheet combined with light-curable resin, allowing the window to conform to the brain's curved surface. The protocol enables long-term, high-resolution, and multiscale imaging-from subcellular structures to large neuronal populations-in awake mice over several months. Key features • This protocol establishes large-scale cranial windows by combining a flexible, biocompatible PEO-CYTOP nanosheet with light-curable resin. • The large-scale cranial window provides long-term optical transparency and mechanical stability, enabling chronic in vivo imaging with minimal motion artifacts. • This approach facilitates multiscale two-photon imaging-from subcellular structures to large-scale neural networks-in awake mice.