Fluorescence microscopy and correlative brightfield videos of mitochondria and vesicles in H9c2 cardiomyoblasts

被引:0
|
作者
Ida S. Opstad
Åsa B. Birgisdottir
Krishna Agarwal
机构
[1] UiT The Arctic University of Norway,Department of Physics and Technology
[2] UiT The Arctic University of Norway,Department of Clinical Medicine
[3] University Hospital of North Norway,Division of Cardiothoracic and Respiratory Medicine
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
This paper presents data acquired to study the dynamics and interactions of mitochondria and subcellular vesicles in living cardiomyoblasts. The study was motivated by the importance of mitochondrial quality control and turnover in cardiovascular health. Although fluorescence microscopy is an invaluable tool, it presents several limitations. Correlative fluorescence and brightfield images (label-free) were therefore acquired with the purpose of achieving virtual labelling via machine learning. In comparison with the fluorescence images of mitochondria, the brightfield images show vesicles and subcellular components, providing additional insights about sub-cellular components. A large part of the data contains correlative fluorescence images of lysosomes and/or endosomes over a duration of up to 400 timepoints (>30 min). The data can be reused for biological inferences about mitochondrial and vesicular morphology, dynamics, and interactions. Furthermore, virtual labelling of mitochondria or subcellular vesicles can be achieved using these datasets. Finally, the data can inspire new imaging experiments for cellular investigations or computational developments. The data is available through two large, open datasets on DataverseNO.
引用
收藏
相关论文
共 50 条
  • [41] Aldosterone induces circadian gene expression of clock genes in H9C2 rat cardiomyoblasts
    Tanaka, K.
    Kawano, H.
    Ashizawa, N.
    Seto, S.
    Yano, K.
    JOURNAL OF HYPERTENSION, 2006, 24 : S339 - S339
  • [42] The role of tenascin C under hyperglycaemic and hypertrophic conditions - In vitro H9c2 rat cardiomyoblasts model
    Goncalves, I. Fonseca
    Acar, E.
    Tretter, E. V.
    Klein, U.
    Kiss, A.
    Podesser, B. K.
    CARDIOVASCULAR RESEARCH, 2018, 114 : S67 - S67
  • [43] Araloside C protects H9c2 cardiomyoblasts against oxidative stress via the modulation of mitochondrial function
    Wang, Min
    Wang, Ruiying
    Xie, Xueheng
    Sun, Guibo
    Sun, Xiaobo
    BIOMEDICINE & PHARMACOTHERAPY, 2019, 117
  • [44] Comparative analysis of stress responses of H9c2 rat cardiomyoblasts following treatment with doxorubicin and tBOOH
    Doehrmann, Mareike
    Schorr, Anne
    Huelsenbeck, Johannes
    Rasmussen, Tine L.
    Issinger, Olaf-Georg
    Fritz, Gerhard
    EXPERIMENTAL CELL RESEARCH, 2012, 318 (06) : 779 - 788
  • [45] Formation of reactive oxygen species (ROS), mitochondrial dysfunction and cell death in H9c2 cardiomyoblasts
    Dodoni, G
    Alexandre, A
    Di Lisa, F
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2004, 36 (05) : 724 - 725
  • [46] Elevated Phosphate Levels Trigger Autophagy-Mediated Cellular Apoptosis in H9c2 Cardiomyoblasts
    Liu, Yao-Lung
    Lin, Kuan-Ho
    Tamilselvi, Shanmugam
    Chen, Wei-Kung
    Shen, Chia-Yao
    Chen, Ray-Jade
    Day, Cecilia Hsuan
    Wu, Hsi-Chin
    Viswanadha, Vijaya Padma
    Huang, Chih-Yang
    CARDIORENAL MEDICINE, 2018, 8 (01) : 31 - 40
  • [47] Single nanomolar treatment with doxorubicin triggers mitochondrial adaptative responses in rat H9c2 cardiomyoblasts
    Ferreira, L. L.
    Cunha-Oliveira, T.
    Oliveira, P. J.
    EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2017, 47 : 20 - 20
  • [48] Proteomic investigation of acute and chronic hypoxia/reoxygenation responsive proteins and pathways in H9C2 cardiomyoblasts
    Oztug, Merve
    Kilinc, Evren
    Durer, Zeynep A. Oztug
    Baloglu, Emel
    TURKISH JOURNAL OF BIOLOGY, 2024, 48 (03) : 192 - 202
  • [49] Formation of reactive oxygen species (ROS), mitochondrial dysfunction and cell death in H9c2 cardiomyoblasts
    Dodoni, G
    Alexandre, A
    Di Lisa, F
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2004, 1658 : 220 - 220
  • [50] Maladaptive response following glucose overload in GLUT4-overexpressing H9C2 cardiomyoblasts
    Stratmann, Bernd
    Eggers, Britta
    Mattern, Yvonne
    de Carvalho, Tayana Silva
    Marcus-Alic, Katrin
    Tschoepe, Diethelm
    DIABETES OBESITY & METABOLISM, 2024, 26 (06): : 2379 - 2389