新しいイメージング手法で脳全体の詳細なRNA解析が可能に(New imaging method enables detailed RNA analysis of the whole brain)

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2024-11-22 カロリンスカ研究所(KI)

カロリンスカ研究所とカロリンスカ大学病院の研究者たちは、新しい顕微鏡技術「TRISCO」を開発し、マウスの全脳を切片化せずに三次元でRNAを詳細に解析することに成功しました。この手法により、脳の複雑な構造を高解像度で観察でき、正常な脳機能や疾患状態の理解が深まります。現在は同時に3種類のRNA分子を解析していますが、今後は「マルチプレックスRNA解析」を用いて約100種類のRNA分子を同時に解析することを目指しています。さらに、TRISCOはマウス脳だけでなく、モルモットの脳や腎臓、心臓、肺などの組織にも適用可能であり、脳疾患の新たな治療法開発に貢献することが期待されています。

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細胞分解能での全脳空間転写解析 Whole-brain spatial transcriptional analysis at cellular resolution

Shigeaki Kanatani, Judith C. Kreutzmann, Yue Li, Zoe West, […], and Per Uhlén
Science  Published:21 Nov 2024
DOI:https://doi.org/10.1126/science.adn9947

新しいイメージング手法で脳全体の詳細なRNA解析が可能に(New imaging method enables detailed RNA analysis of the whole brain)

Editor’s summary

Spatial transcriptomics is a powerful method that measures the localization of mRNA molecules. When applying this approach in tissues, analysis is typically limited to thin sections rather than full volumes. Kanatani et al. developed a brain tissue–clearing method called TRISCO that enables three-dimensional in situ hybridization on the whole brain, allowing the visualization of specific mRNAs in the complete brain at cellular resolution. Using TRISCO, the authors monitored the expression of immediate early genes after administration of the antiobesity drug semaglutide in mice, finding increased expression in brain regions associated with obesity. TRISCO thus enables the study of intricate gene expression patterns spanning the whole brain at single-cell resolution. —Mattia Maroso

Abstract

Recent advances in RNA analysis have deepened our understanding of cellular states in biological tissues. However, a substantial gap remains in integrating RNA expression data with spatial context across organs, primarily owing to the challenges associated with RNA detection within intact tissue volumes. Here, we developed Tris buffer–mediated retention of in situ hybridization chain reaction signal in cleared organs (TRISCO), an effective tissue-clearing method designed for whole-brain spatial three-dimensional (3D) RNA imaging. TRISCO resolved several crucial issues, including the preservation of RNA integrity, achieving uniform RNA labeling, and enhancing tissue transparency. We tested TRISCO using a broad range of cell-identity markers, noncoding and activity-dependent RNAs, within diverse organs of varying sizes and species. TRISCO thus emerges as a powerful tool for single-cell, whole-brain, 3D imaging that enables comprehensive transcriptional spatial analysis across the entire brain.

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