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Two-Photon Excitation Imaging of Pancreatic Islets With Various Fluorescent Probes

¹ Department of Cell Physiology, National Institute for Physiological Sciences, Okazaki, Japan
² University of Tokyo, School of Medicine, Bunkyo-ku, Tokyo, Japan
³ Department of Molecular Physiology, Tokyo Metropolitan Institute for Neuroscience, Fuchu, Tokyo, Japan
⁴ Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Corporation (JST), Hongo, Bunkyo-ku, Japan
⁵ CREST of JST, Kawaguchi, Saitama, Japan

Various fluorescent probes were assessed for investigating intact islets of Langerhans using two-photon excitation imaging. Polar fluorescent tracers applied on the outside rapidly (within 3 min) penetrated deep into the islets via microvessels. Likewise, an adenovirus carrying a Ca²⁺-sensitive green fluorescent protein mutant gene, yellow cameleon 2.1, was successfully transfected and enabled ratiometric cytosolic Ca²⁺ measurement of cells in the deep layers of the islets. Interestingly, FM1-43, which is lipophilic and does not permeate the plasma membrane, also rapidly reached deep cell layers of the islets. In contrast, lipophilic fluorescent probes that permeate the plasma membrane (for example, fura-2-acetoxymethyl and BODIPY-forskolin) accumulated in the superficial cell layers of the islets, even 30 min after application. Thus, two-photon excitation imaging of pancreatic islets is a promising method for clarifying signaling mechanisms of islet cells, particularly when it is combined with membrane-impermeable probes. In addition, our data suggest that membrane-permeable antagonists may affect only the superficial cell layers of islets, and so their negative effects should be interpreted with caution.

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