2021年11月10日
Advances in Two-Photon Imaging in Plants
Plant and Cell Physiology
- 巻
- 62
- 号
- 8
- 開始ページ
- 1224
- 終了ページ
- 1230
- 記述言語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1093/pcp/pcab062
- 出版者・発行元
- Oxford University Press (OUP)
Abstract
Live and deep imaging play a significant role in the physiological and biological study of organisms. Two-photon excitation microscopy (2PEM), also known as multiphoton excitation microscopy, is a fluorescent imaging technique that allows deep imaging of living tissues. Two-photon lasers use near-infrared (NIR) pulse lasers that are less invasive and permit deep tissue penetration. In this review, recent advances in two-photon imaging and their applications in plant studies are discussed. Compared to confocal microscopy, NIR 2PEM exhibits reduced plant-specific autofluorescence, thereby achieving greater depth and high-resolution imaging in plant tissues. Fluorescent proteins with long emission wavelengths, such as orange–red fluorescent proteins, are particularly suitable for two-photon live imaging in plants. Furthermore, deep- and high-resolution imaging was achieved using plant-specific clearing methods. In addition to imaging, optical cell manipulations can be performed using femtosecond pulsed lasers at the single cell or organelle level. Optical surgery and manipulation can reveal cellular communication during development. Advances in in vivo imaging using 2PEM will greatly benefit biological studies in plant sciences.
Live and deep imaging play a significant role in the physiological and biological study of organisms. Two-photon excitation microscopy (2PEM), also known as multiphoton excitation microscopy, is a fluorescent imaging technique that allows deep imaging of living tissues. Two-photon lasers use near-infrared (NIR) pulse lasers that are less invasive and permit deep tissue penetration. In this review, recent advances in two-photon imaging and their applications in plant studies are discussed. Compared to confocal microscopy, NIR 2PEM exhibits reduced plant-specific autofluorescence, thereby achieving greater depth and high-resolution imaging in plant tissues. Fluorescent proteins with long emission wavelengths, such as orange–red fluorescent proteins, are particularly suitable for two-photon live imaging in plants. Furthermore, deep- and high-resolution imaging was achieved using plant-specific clearing methods. In addition to imaging, optical cell manipulations can be performed using femtosecond pulsed lasers at the single cell or organelle level. Optical surgery and manipulation can reveal cellular communication during development. Advances in in vivo imaging using 2PEM will greatly benefit biological studies in plant sciences.
- リンク情報
-
- DOI
- https://doi.org/10.1093/pcp/pcab062
- PubMed
- https://www.ncbi.nlm.nih.gov/pubmed/34019083
- 共同研究・競争的資金等の研究課題
- 細胞運命操作による植物生殖システムのリモデリング(研究代表者:丸山大輔)
- 共同研究・競争的資金等の研究課題
- 1細胞追跡による花粉の精細胞の運命と受精能を決定するメカニズムの解明
- 共同研究・競争的資金等の研究課題
- イメージングと遺伝子発現を基盤とした植物の受精に必須な遺伝子の解析
- URL
- http://academic.oup.com/pcp/advance-article-pdf/doi/10.1093/pcp/pcab062/40325087/pcab062.pdf
- URL
- https://academic.oup.com/pcp/article-pdf/62/8/1224/41119175/pcab062.pdf
- ID情報
-
- DOI : 10.1093/pcp/pcab062
- ISSN : 0032-0781
- eISSN : 1471-9053
- PubMed ID : 34019083