Molecules and Cells

Cited by CrossRef (36)

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  2. Ayeshah A. Rosdah, Jessica K. Holien, Lea M. D. Delbridge, Gregory J. Dusting, Shiang Y. Lim. Mitochondrial fission – a drug target for cytoprotection or cytodestruction?. Pharmacol Res Perspect 2016;4
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  3. Amy C. Keller, Hussain Badani, P. Mason McClatchey, Nicholas L. Baird, Jacqueline L. Bowlin, Ron Bouchard, Guey-Chuen Perng, Jane E. B. Reusch, Benedikt B. Kaufer, Don Gilden, Aamir Shahzad, Peter G. E. Kennedy, Randall J. Cohrs. Varicella zoster virus infection of human fetal lung cells alters mitochondrial morphology. J. Neurovirol. 2016;22:674
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  4. Rui-Qi Jiang, Qi-Qi Li, Rui Sheng. Mitochondria associated ER membranes and cerebral ischemia: Molecular mechanisms and therapeutic strategies. Pharmacological Research 2023;191:106761
    https://doi.org/10.1016/j.phrs.2023.106761
  5. Laurent Chatel-Chaix, Mirko Cortese, Inés Romero-Brey, Silke Bender, Christopher John Neufeldt, Wolfgang Fischl, Pietro Scaturro, Nicole Schieber, Yannick Schwab, Bernd Fischer, Alessia Ruggieri, Ralf Bartenschlager. Dengue Virus Perturbs Mitochondrial Morphodynamics to Dampen Innate Immune Responses. Cell Host & Microbe 2016;20:342
    https://doi.org/10.1016/j.chom.2016.07.008
  6. Mi Ra Noh, Chang-Hoon Woo, Mae-Ja Park, Jee In Kim, Kwon Moo Park. Ablation of C/EBP homologous protein attenuates renal fibrosis after ureteral obstruction by reducing autophagy and microtubule disruption. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 2018;1864:1634
    https://doi.org/10.1016/j.bbadis.2018.02.001
  7. Komal Panchal, Anand Krishna Tiwari. Mitochondrial dynamics, a key executioner in neurodegenerative diseases. Mitochondrion 2019;47:151
    https://doi.org/10.1016/j.mito.2018.11.002
  8. Liyi Li, Qin Chen, Yaojun Yu, Hui Chen, Mingdong Lu, Yingpeng Huang, Pihong Li, Hong Chang. RKI‐1447 suppresses colorectal carcinoma cell growth via disrupting cellular bioenergetics and mitochondrial dynamics. J Cell Physiol 2020;235:254
    https://doi.org/10.1002/jcp.28965
  9. Vanessa Hertlein, Hector Flores-Romero, Kushal K Das, Sebastian Fischer, Michael Heunemann, Maria Calleja-Felipe, Shira Knafo, Katharina Hipp, Klaus Harter, Julia C Fitzgerald, Ana J García-Sáez. MERLIN: a novel BRET-based proximity biosensor for studying mitochondria–ER contact sites. Life Sci. Alliance 2020;3:e201900600
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  10. Arianna Di Daniele, Luca Simula, Silvia Campello. Mitochondrial Regulation. 2020.
    https://doi.org/10.1007/978-1-0716-1433-4_16
  11. Manuela D’Eletto, Federica Rossin, Luca Occhigrossi, Maria Grazia Farrace, Danilo Faccenda, Radha Desai, Saverio Marchi, Giulia Refolo, Laura Falasca, Manuela Antonioli, Fabiola Ciccosanti, Gian Maria Fimia, Paolo Pinton, Michelangelo Campanella, Mauro Piacentini. Transglutaminase Type 2 Regulates ER-Mitochondria Contact Sites by Interacting with GRP75. Cell Reports 2018;25:3573
    https://doi.org/10.1016/j.celrep.2018.11.094
  12. Joana Sá-Pessoa, Sara López-Montesino, Kornelia Przybyszewska, Isabel Rodríguez-Escudero, Helina Marshall, Adelia Ova, Gunnar N. Schroeder, Peter Barabas, María Molina, Tim Curtis, Víctor J. Cid, José A. Bengoechea. A trans-kingdom T6SS effector induces the fragmentation of the mitochondrial network and activates innate immune receptor NLRX1 to promote infection. Nat Commun 2023;14
    https://doi.org/10.1038/s41467-023-36629-3
  13. Volha I. Summerhill, Vasily N. Sukhorukov, Ali H. Eid, Ludmila V. Nedosugova, Igor A. Sobenin, Alexander N. Orekhov. Pathophysiological Aspects of the Development of Abdominal Aortic Aneurysm with a Special Focus on Mitochondrial Dysfunction and Genetic Associations. 2021;12:55
    https://doi.org/10.1515/bmc-2021-0007
  14. Xingjuan Shi, Xuan Jiang, Congwei Chen, Yu Zhang, Xiaoou Sun. The interconnections between the microtubules and mitochondrial networks in cardiocerebrovascular diseases: Implications for therapy. Pharmacological Research 2022;184:106452
    https://doi.org/10.1016/j.phrs.2022.106452
  15. Yen-Lin Huang, Yi-Jung Chen, Yi-Hsiu Juan, Shang-Gin Wu, Kuei-Pin Chung. Prognostic significance of dynamin-related protein 1 expression in advanced lung adenocarcinoma. Pathology - Research and Practice 2022;234:153931
    https://doi.org/10.1016/j.prp.2022.153931
  16. Orsolya Horvath, Katalin Ordog, Kitti Bruszt, Nikoletta Kalman, Dominika Kovacs, Balazs Radnai, Ferenc Gallyas, Kalman Toth, Robert Halmosi, Laszlo Deres, Hao Zhou. Modulation of Mitochondrial Quality Control Processes by BGP-15 in Oxidative Stress Scenarios: From Cell Culture to Heart Failure. Oxidative Medicine and Cellular Longevity 2021;2021:1
    https://doi.org/10.1155/2021/6643871
  17. Satoru Eguchi, Tatsuo Kawai, Rosario Scalia, Victor Rizzo. Understanding Angiotensin II Type 1 Receptor Signaling in Vascular Pathophysiology. Hypertension 2018;71:804
    https://doi.org/10.1161/HYPERTENSIONAHA.118.10266
  18. Sukrut C. Kamerkar, Felix Kraus, Alice J. Sharpe, Thomas J. Pucadyil, Michael T. Ryan. Dynamin-related protein 1 has membrane constricting and severing abilities sufficient for mitochondrial and peroxisomal fission. Nat Commun 2018;9
    https://doi.org/10.1038/s41467-018-07543-w
  19. Manuel Albert, Martina Bécares, Michela Falqui, Carlos Fernández-Lozano, Susana Guerra. ISG15, a Small Molecule with Huge Implications: Regulation of Mitochondrial Homeostasis. Viruses 2018;10:629
    https://doi.org/10.3390/v10110629
  20. Fan Zheng, Bowen Jia, Fenfen Dong, Ling Liu, Faiz Rasul, Jiajia He, Chuanhai Fu. Glucose starvation induces mitochondrial fragmentation depending on the dynamin GTPase Dnm1/Drp1 in fission yeast. Journal of Biological Chemistry 2019;294:17725
    https://doi.org/10.1074/jbc.RA119.010185
  21. Heidi Zinecker, Djamila Ouaret, Daniel Ebner, Moritz M. Gaidt, Steve Taylor, Anna Aulicino, Marta Jagielowicz, Veit Hornung, Alison Simmons. ICG-001 affects DRP1 activity and ER stress correlative with its anti-proliferative effect. Oncotarget 2017;8:106764
    https://doi.org/10.18632/oncotarget.22264
  22. Thomas J. Krzystek, Rupkatha Banerjee, Layne Thurston, JianQiao Huang, Kelsey Swinter, Saad Navid Rahman, Tomas L. Falzone, Shermali Gunawardena. Differential mitochondrial roles for α-synuclein in DRP1-dependent fission and PINK1/Parkin-mediated oxidation. Cell Death Dis 2021;12
    https://doi.org/10.1038/s41419-021-04046-3
  23. Mohsin Khan, Gulam Hussain Syed, Seong-Jun Kim, Aleem Siddiqui. Mitochondrial dynamics and viral infections: A close nexus. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 2015;1853:2822
    https://doi.org/10.1016/j.bbamcr.2014.12.040
  24. Nicolas Tremblay, Wesley Freppel, Aïssatou Aïcha Sow, Laurent Chatel-Chaix. The Interplay between Dengue Virus and the Human Innate Immune System: A Game of Hide and Seek. Vaccines 2019;7:145
    https://doi.org/10.3390/vaccines7040145
  25. Wan-Ting Jin, Jia-Yin Guan, Xin-Yi Dai, Gong-Ji Wu, Le-Ping Zhang, Kenneth B. Storey, Jia-Yong Zhang, Rong-Quan Zheng, Dan-Na Yu. Mitochondrial gene expression in different organs of Hoplobatrachus rugulosus from China and Thailand under low-temperature stress. BMC Zool 2022;7
    https://doi.org/10.1186/s40850-022-00128-7
  26. Sri Rahavi Boovarahan, Gino A. Kurian. Investigating the role of DNMT1 gene expression on myocardial ischemia reperfusion injury in rat and associated changes in mitochondria. Biochimica et Biophysica Acta (BBA) - Bioenergetics 2022;1863:148566
    https://doi.org/10.1016/j.bbabio.2022.148566
  27. Anna Melkov, Uri Abdu. Regulation of long-distance transport of mitochondria along microtubules. Cell. Mol. Life Sci. 2018;75:163
    https://doi.org/10.1007/s00018-017-2590-1
  28. Jeffrey D. Marshall, Isabel Bazan, Yi Zhang, Wassim H. Fares, Patty J. Lee. Mitochondrial dysfunction and pulmonary hypertension: cause, effect, or both. American Journal of Physiology-Lung Cellular and Molecular Physiology 2018;314:L782
    https://doi.org/10.1152/ajplung.00331.2017
  29. Sreesha Sree, Ilmari Parkkinen, Anna Their, Mikko Airavaara, Eija Jokitalo. Morphological Heterogeneity of the Endoplasmic Reticulum within Neurons and Its Implications in Neurodegeneration. Cells 2021;10:970
    https://doi.org/10.3390/cells10050970
  30. Anthony R. Anzell, Rita Maizy, Karin Przyklenk, Thomas H. Sanderson. Mitochondrial Quality Control and Disease: Insights into Ischemia-Reperfusion Injury. Mol Neurobiol 2018;55:2547
    https://doi.org/10.1007/s12035-017-0503-9
  31. Shanhui Ren, Chan Ding, Yingjie Sun. Morphology Remodeling and Selective Autophagy of Intracellular Organelles during Viral Infections. IJMS 2020;21:3689
    https://doi.org/10.3390/ijms21103689
  32. Michael Schrader, Luis F. Godinho, Joseph L. Costello, Markus Islinger. The different facets of organelle interplay—an overview of organelle interactions. Front. Cell Dev. Biol. 2015;3
    https://doi.org/10.3389/fcell.2015.00056
  33. Samuel Rout, Jon Paulin Zumthor, Elisabeth M. Schraner, Carmen Faso, Adrian B. Hehl, Krishan Kumar. An Interactome-Centered Protein Discovery Approach Reveals Novel Components Involved in Mitosome Function and Homeostasis in Giardia lamblia. PLoS Pathog 2016;12:e1006036
    https://doi.org/10.1371/journal.ppat.1006036
  34. Chinaemere Igwebuike, Julia Yaglom, Leah Huiting, Hui Feng, Joshua D. Campbell, Zhiyong Wang, Andrea Havasi, David Pimentel, Michael Y. Sherman, Steven C. Borkan. Cross organelle stress response disruption promotes gentamicin-induced proteotoxicity. Cell Death Dis 2020;11
    https://doi.org/10.1038/s41419-020-2382-7
  35. Jingjing Jia, Haiqiang Jin, Ding Nan, Weiwei Yu, Yining Huang. New insights into targeting mitochondria in ischemic injury. Apoptosis 2021;26:163
    https://doi.org/10.1007/s10495-021-01661-5
  36. Michael Schrader, Joseph L. Costello, Luis F. Godinho, Afsoon S. Azadi, Markus Islinger. Proliferation and fission of peroxisomes — An update. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 2016;1863:971
    https://doi.org/10.1016/j.bbamcr.2015.09.024