Laser scanning reflection-matrix microscopy for aberration-free imaging through intact mouse skull
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Seokchan Yoon | - |
dc.contributor.author | Hojun Lee | - |
dc.contributor.author | Jin Hee Hong | - |
dc.contributor.author | Yong-Sik Lim | - |
dc.contributor.author | Wonshik Choi | - |
dc.date.accessioned | 2021-01-07T06:30:12Z | - |
dc.date.accessioned | 2021-01-07T06:30:12Z | - |
dc.date.available | 2021-01-07T06:30:12Z | - |
dc.date.available | 2021-01-07T06:30:12Z | - |
dc.date.created | 2020-12-03 | - |
dc.date.issued | 2020-11 | - |
dc.identifier.issn | 2041-1723 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/9007 | - |
dc.description.abstract | A mouse skull is a barrier for high-resolution optical imaging because its thick and inhomogeneous internal structures induce complex aberrations varying drastically from position to position. Invasive procedures creating either thinned-skull or open-skull windows are often required for the microscopic imaging of brain tissues underneath. Here, we propose a label-free imaging modality termed laser scanning reflection-matrix microscopy for recording the amplitude and phase maps of reflected waves at non-confocal points as well as confocal points. The proposed method enables us to find and computationally correct up to 10,000 angular modes of aberrations varying at every 10 × 10 µm2 patch in the sample plane. We realized reflectance imaging of myelinated axons in vivo underneath an intact mouse skull, with an ideal diffraction-limited spatial resolution of 450 nm. Furthermore, we demonstrated through-skull two-photon fluorescence imaging of neuronal dendrites and their spines by physically correcting the aberrations identified from the reflection matrix | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | NATURE RESEARCH | - |
dc.title | Laser scanning reflection-matrix microscopy for aberration-free imaging through intact mouse skull | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000593979500002 | - |
dc.identifier.scopusid | 2-s2.0-85095949274 | - |
dc.identifier.rimsid | 73834 | - |
dc.contributor.affiliatedAuthor | Seokchan Yoon | - |
dc.contributor.affiliatedAuthor | Hojun Lee | - |
dc.contributor.affiliatedAuthor | Jin Hee Hong | - |
dc.contributor.affiliatedAuthor | Wonshik Choi | - |
dc.identifier.doi | 10.1038/s41467-020-19550-x | - |
dc.identifier.bibliographicCitation | Nature Communications, v.11, no.1, pp.1 - 12 | - |
dc.citation.title | Nature Communications | - |
dc.citation.volume | 11 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 1 | - |
dc.citation.endPage | 12 | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | OPTICAL COHERENCE MICROSCOPY | - |
dc.subject.keywordPlus | ADAPTIVE OPTICS | - |
dc.subject.keywordPlus | VIVO | - |
dc.subject.keywordPlus | RESOLUTION | - |
dc.subject.keywordPlus | LIMIT | - |
dc.subject.keywordPlus | DEEP | - |
dc.subject.keywordPlus | TOMOGRAPHY | - |
dc.subject.keywordPlus | BRAIN | - |
dc.subject.keywordAuthor | OPTICAL COHERENCE MICROSCOPY | - |
dc.subject.keywordAuthor | ADAPTIVE OPTICS | - |
dc.subject.keywordAuthor | VIVO | - |
dc.subject.keywordAuthor | RESOLUTION | - |
dc.subject.keywordAuthor | LIMIT | - |
dc.subject.keywordAuthor | DEEP | - |
dc.subject.keywordAuthor | TOMOGRAPHY | - |
dc.subject.keywordAuthor | BRAIN | - |