Optimization of Fluorescent Labeling for In Vivo Nanoimaging of Sarcomeres in the Mouse Heart.

The present study was conducted to systematically investigate the optimal viral titer as well as the volume of the adenovirus vector (ADV) that expresses α-actinin-AcGFP in the Z-disks of myocytes in the left ventricle (LV) of mice. An injection of 10 μL ADV at viral titers of 2 to 4 × 1011 viral pa...

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Publicado en:BioMed Research International Vol. 2018; pp. 1 - 9
Autores principales: Kobirumaki-Shimozawa, Fuyu, Shimozawa, Togo, Oyama, Kotaro, Kushida, Yasuharu, Terui, Takako, Ishiwata, Shin’ichi, Fukuda, Norio
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 8/23/2018
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 8/23/2018
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2018/4349170
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        atl: Optimization of Fluorescent Labeling for In Vivo Nanoimaging of Sarcomeres in the Mouse Heart.
      aug:
        au:
          Kobirumaki-Shimozawa, Fuyu
          Shimozawa, Togo
          Oyama, Kotaro
          Kushida, Yasuharu
          Terui, Takako
          Ishiwata, Shin’ichi
          Fukuda, Norio
        affil: Department of Cell Physiology, The Jikei University School of Medicine, 3-25-8 Nishi-shinbashi, Minato-ku, Tokyo 105-8461, Japan
      sug:
        subj:
          Nanotechnology
          Muscle Fibers Anatomy and Histology
          Staining and Labeling Methods
          Light
          Viral Load
          DNA Viruses
          Gene Expression
          Muscle Proteins
          Myocytes, Cardiac Analysis
          Heart Ventricle, Left Analysis
          Animal Studies
          Mice
          In Vivo Studies
          Heart Arrest
          Anesthesia
      ab: The present study was conducted to systematically investigate the optimal viral titer as well as the volume of the adenovirus vector (ADV) that expresses α-actinin-AcGFP in the Z-disks of myocytes in the left ventricle (LV) of mice. An injection of 10 μL ADV at viral titers of 2 to 4 × 1011 viral particles per mL (VP/mL) into the LV epicardial surface consistently expressed α-actinin-AcGFP in myocytes in vivo, with the fraction of AcGFP-expressing myocytes at ~10%. Our analysis revealed that SL was ~1.90-2.15 μm upon heart arrest via deep anesthesia. Likewise, we developed a novel fluorescence labeling method of the T-tubular system by treating the LV surface with CellMask Orange (CellMask). We found that the T-tubular distance was ~2.10-2.25 μm, similar to SL, in the healthy heart in vivo. Therefore, the present high-precision visualization method for the Z-disks or the T-tubules is beneficial to unveiling the mechanisms of myocyte contraction in health and disease in vivo.
      pubtype: Academic Journal
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        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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