Evidence map›Paper›PMID 38438546›Full record

ArticleCommunications biology2024

Large-scale cranial window for in vivo mouse brain imaging utilizing fluoropolymer nanosheet and light-curable resin.

Taiga Takahashi, Hong Zhang, Masakazu Agetsuma, Junichi Nabekura, Kohei Otomo, Yosuke Okamura, Tomomi Nemoto

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Taiga TakahashiDivision of Biophotonics, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Higashiyama 5-1, Myodaiji, Okazaki, Aichi, 444-8787, Japan.ORCID 0000-0002-8821-2125
Hong ZhangMicro/Nano Technology Center, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa, 259-1292, Japan.
Masakazu AgetsumaDivision of Homeostatic Development, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, 444-8585, Japan.ORCID 0000-0002-8606-4886
Junichi NabekuraSchool of Life Science, The Graduate University for Advanced Studies (SOKENDAI), Higashiyama 5-1, Myodaiji, Okazaki, Aichi, 444-8787, Japan.ORCID 0000-0001-5834-6272
Kohei OtomoDivision of Biophotonics, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Higashiyama 5-1, Myodaiji, Okazaki, Aichi, 444-8787, Japan.ORCID 0000-0002-5322-6295
Yosuke OkamuraMicro/Nano Technology Center, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa, 259-1292, Japan.
Tomomi NemotoDivision of Biophotonics, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Higashiyama 5-1, Myodaiji, Okazaki, Aichi, 444-8787, Japan. tn@nips.ac.jp.ORCID 0000-0001-6102-1495
National Institutes of Natural Sciences · JPTokai University · JPTokyo University of Science · JP

Funding

Japan Agency for Medical Research and Development (AMED) 19dm0207078Japan Agency for Medical Research and Development (AMED) 19dm0207086Japan Agency for Medical Research and Development (AMED) 19dm0207087Japan Society for the Promotion of Science London (JSPS London) JP18H04744MEXT | Japan Science and Technology Agency (JST) JPMJAX2228MEXT | Japan Society for the Promotion of Science (JSPS) JP16H06280MEXT | Japan Society for the Promotion of Science (JSPS) JP20H05669MEXT | Japan Society for the Promotion of Science (JSPS) JP21H02801MEXT | Japan Society for the Promotion of Science (JSPS) JP21J14773MEXT | Japan Society for the Promotion of Science (JSPS) JP22H04926MEXT | Japan Society for the Promotion of Science (JSPS) JP22H05081MEXT | Japan Society for the Promotion of Science (JSPS) JP22H05519MEXT | Japan Society for the Promotion of Science (JSPS) JP22K21353MEXT | Japan Society for the Promotion of Science (JSPS) JP23K14294MEXT | JST | Core Research for Evolutional Science and Technology (CREST) JPMJCR20E4
6 · The paper itself

Abstract

Two-photon microscopy enables in vivo imaging of neuronal activity in mammalian brains at high resolution. However, two-photon imaging tools for stable, long-term, and simultaneous study of multiple brain regions in same mice are lacking. Here, we propose a method to create large cranial windows covering such as the whole parietal cortex and cerebellum in mice using fluoropolymer nanosheets covered with light-curable resin (termed the 'Nanosheet Incorporated into light-curable REsin' or NIRE method). NIRE method can produce cranial windows conforming the curved cortical and cerebellar surfaces, without motion artifacts in awake mice, and maintain transparency for >5 months. In addition, we demonstrate that NIRE method can be used for in vivo two-photon imaging of neuronal ensembles, individual neurons and subcellular structures such as dendritic spines. The NIRE method can facilitate in vivo large-scale analysis of heretofore inaccessible neural processes, such as the neuroplastic changes associated with maturation, learning and neural pathogenesis.

Indexed as

ArtifactsFluorocarbon PolymersAnimalsBrainCerebellumMammalsMiceNeuroimagingResins, PlantFluorocarbon PolymersResins, Plant

Identifiers

PMID38438546
PMCPMC10912766
OpenAlexW4392375578

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.