en Experimental Neurobiology

Cited by CrossRef (30)

  1. Hyung-Joo Chung, Muwoong Kim, Junyang Jung, Na Young Jeong. Inhibition of Neuronal Nitric Oxide Synthase by Ethyl Pyruvate in Schwann Cells Protects Against Peripheral Nerve Degeneration. Neurochem Res 2019;44:1964
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  2. Seung Baek Han, Hyukmin Kim, Hyunkyoung Lee, Matthew Grove, George M. Smith, Young-Jin Son. Postinjury Induction of Activated ErbB2 Selectively Hyperactivates Denervated Schwann Cells and Promotes Robust Dorsal Root Axon Regeneration. J. Neurosci. 2017;37:10955
    https://doi.org/10.1523/JNEUROSCI.0903-17.2017
  3. Maria Domenica Sanna, Carla Ghelardini, Nicoletta Galeotti. Spinal astrocytic c-Jun N-terminal kinase (JNK) activation as counteracting mechanism to the amitriptyline analgesic efficacy in painful peripheral neuropathies. European Journal of Pharmacology 2017;798:85
    https://doi.org/10.1016/j.ejphar.2017.01.025
  4. J Cao, J-s Wang, X-h Ren, W-d Zang. Spinal sample showing p-JNK and P38 associated with the pain signaling transduction of glial cell in neuropathic pain. Spinal Cord 2015;53:92
    https://doi.org/10.1038/sc.2014.188
  5. Jennifer Soto, Paula V. Monje. Axon contact-driven Schwann cell dedifferentiation. Glia 2017;65:864
    https://doi.org/10.1002/glia.23131
  6. Jinkun Wen, Dandan Tan, Lixia Li, Xianghai Wang, Mengjie Pan, Jiasong Guo. RhoA regulates Schwann cell differentiation through JNK pathway. Experimental Neurology 2018;308:26
    https://doi.org/10.1016/j.expneurol.2018.06.013
  7. Victoria J. Horak, Abby Mishory, Shivani Baisiwala, Atique U. Ahmed. Comprehensive Pharmacology. 2018.
    https://doi.org/10.1016/B978-0-12-820472-6.00062-1
  8. Angélique Boerboom, Valérie Dion, Alain Chariot, Rachelle Franzen. Molecular Mechanisms Involved in Schwann Cell Plasticity. Front. Mol. Neurosci. 2017;10
    https://doi.org/10.3389/fnmol.2017.00038
  9. L. R. Galieva, Y. O. Mukhamedshina, E. R. Akhmetzyanova, Z. E. Gilazieva, S. S. Arkhipova, E. E. Garanina, A. A. Rizvanov. Influence of Genetically Modified Human Umbilical Cord Blood Mononuclear Cells on the Expression of Schwann Cell Molecular Determinants in Spinal Cord Injury. Stem Cells International 2018;2018:1
    https://doi.org/10.1155/2018/4695275
  10. Afonso Malheiro, Adrián Seijas-Gamardo, Abhishek Harichandan, Carlos Mota, Paul Wieringa, Lorenzo Moroni. Development of an In Vitro Biomimetic Peripheral Neurovascular Platform. ACS Appl. Mater. Interfaces 2022;14:31567
    https://doi.org/10.1021/acsami.2c03861
  11. Hwan Tae Park, Jong Kuk Kim, Nicolas Tricaud. The conceptual introduction of the “demyelinating Schwann cell” in peripheral demyelinating neuropathies. Glia 2019;67:571
    https://doi.org/10.1002/glia.23509
  12. Aseer Intisar, Hanwoong Woo, Hyun Gyu Kang, Woon-Hae Kim, Hyun Young Shin, Min Young Kim, Yu Seon Kim, Yun Jeoung Mo, Yun-Il Lee, Minseok S. Kim. Electroceutical approach ameliorates intracellular PMP22 aggregation and promotes pro-myelinating pathways in a CMT1A in vitro model. Biosensors and Bioelectronics 2023;224:115055
    https://doi.org/10.1016/j.bios.2022.115055
  13. Renzo Mancuso, Anna Martínez-Muriana, Tatiana Leiva, David Gregorio, Lorena Ariza, Marta Morell, Jesús Esteban-Pérez, Alberto García-Redondo, Ana C. Calvo, Gabriela Atencia-Cibreiro, Gabriel Corfas, Rosario Osta, Assumpció Bosch, Xavier Navarro. Neuregulin-1 promotes functional improvement by enhancing collateral sprouting in SOD1G93A ALS mice and after partial muscle denervation. Neurobiology of Disease 2016;95:168
    https://doi.org/10.1016/j.nbd.2016.07.023
  14. Nicolas Tricaud, Hwan Tae Park. Wallerian demyelination: chronicle of a cellular cataclysm. Cell. Mol. Life Sci. 2017;74:4049
    https://doi.org/10.1007/s00018-017-2565-2
  15. Jun Yang, Jun Cao, Su Min, Ping Li, Feng Lv, Li Ren. Recombinant human neuregulin-1 alleviates immobilization-induced neuromuscular dysfunction via neuregulin-1/ErbB signaling pathway in rat. Archives of Biochemistry and Biophysics 2023;743:109631
    https://doi.org/10.1016/j.abb.2023.109631
  16. William M. Valentine. Toxic Peripheral Neuropathies: Agents and Mechanisms. Toxicol Pathol 2020;48:152
    https://doi.org/10.1177/0192623319854326
  17. Emilia Manole, Alexandra Eugenia Bastian, Ana Maria Oproiu, Monica Teodora Neagu, Carolina Constantin, Gheorghita Isvoranu. Demyelination Disorders. 2020.
    https://doi.org/10.5772/intechopen.91805
  18. So Young Jang, Yoon Kyung Shin, So Young Park, Joo Youn Park, Hye Jeong Lee, Young Hyun Yoo, Jong Kuk Kim, Hwan Tae Park. Autophagic myelin destruction by schwann cells during wallerian degeneration and segmental demyelination. Glia 2016;64:730
    https://doi.org/10.1002/glia.22957
  19. Ting Liu, Yang Wang, Laijin Lu, Yi Liu. SPIONs mediated magnetic actuation promotes nerve regeneration by inducing and maintaining repair-supportive phenotypes in Schwann cells. J Nanobiotechnol 2022;20
    https://doi.org/10.1186/s12951-022-01337-5
  20. Gang Chen, Xiaohe Luo, Wenjin Wang, Yimei Wang, Fei Zhu, Wei Wang. Interleukin-1β Promotes Schwann Cells De-Differentiation in Wallerian Degeneration via the c-JUN/AP-1 Pathway. Front. Cell. Neurosci. 2019;13
    https://doi.org/10.3389/fncel.2019.00304
  21. Kristjan R Jessen, Peter Arthur‐Farraj. Repair Schwann cell update: Adaptive reprogramming, EMT, and stemness in regenerating nerves. Glia 2019;67:421
    https://doi.org/10.1002/glia.23532
  22. Yoo Lim Chun, Sumin Lee, Ki-Hoon Park, Chan Park, Youngbuhm Huh, Na Young Jeong, Junyang Jung. Protective and therapeutic effect of (S)-ginsenoside F1 on peripheral nerve degeneration targeting Schwann cells: a pharmaco-neuroanatomical approach. Anat Sci Int 2022;97:79
    https://doi.org/10.1007/s12565-021-00630-x
  23. Jianwei Lv, Xiaolei Sun, Jianxiong Ma, Xinlong Ma, Yang Zhang, Fengbo Li, Yanjun Li, Zhihu Zhao. Netrin-1 induces the migration of Schwann cells via p38 MAPK and PI3K-Akt signaling pathway mediated by the UNC5B receptor. Biochemical and Biophysical Research Communications 2015;464:263
    https://doi.org/10.1016/j.bbrc.2015.06.140
  24. Xiumei Fu, Zhaoxue Tong, Qi Li, Qingfei Niu, Zhe Zhang, Xiaojie Tong, Lei Tong, Xu Zhang. Induction of adipose-derived stem cells into Schwann-like cells and observation of Schwann-like cell proliferation. 2016;14:1187
    https://doi.org/10.3892/mmr.2016.5367
  25. Giuseppe Musumeci, Gian Leggio, Rubina Marzagalli, Ghaith Al-Badri, Filippo Drago, Alessandro Castorina. Identification of Dysregulated microRNA Networks in Schwann Cell-Like Cultures Exposed to Immune Challenge: Potential Crosstalk with the Protective VIP/PACAP Neuropeptide System. IJMS 2018;19:981
    https://doi.org/10.3390/ijms19040981
  26. Nicolas Tricaud, Benoit Gautier, Jade Berthelot, Sergio Gonzalez, Gerben Van Hameren. Traumatic and Diabetic Schwann Cell Demyelination Is Triggered by a Transient Mitochondrial Calcium Release through Voltage Dependent Anion Channel 1. Biomedicines 2022;10:1447
    https://doi.org/10.3390/biomedicines10061447
  27. Andrii Klymenko, David Lutz. Melatonin signalling in Schwann cells during neuroregeneration. Front. Cell Dev. Biol. 2022;10
    https://doi.org/10.3389/fcell.2022.999322
  28. Hozo Matsuoka, Kosuke Ebina, Hiroyuki Tanaka, Makoto Hirao, Toru Iwahashi, Takaaki Noguchi, Koji Suzuki, Shunsuke Nishimoto, Tsuyoshi Murase, Hideki Yoshikawa. Administration of Oxygen Ultra-Fine Bubbles Improves Nerve Dysfunction in a Rat Sciatic Nerve Crush Injury Model. IJMS 2018;19:1395
    https://doi.org/10.3390/ijms19051395
  29. Sergio Gonzalez, Jade Berthelot, Jennifer Jiner, Claire Perrin-Tricaud, Ruani Fernando, Roman Chrast, Guy Lenaers, Nicolas Tricaud. Blocking mitochondrial calcium release in Schwann cells prevents demyelinating neuropathies. 2016;126:1023
    https://doi.org/10.1172/JCI84505
  30. Hozo Matsuoka, Hiroyuki Tanaka, Junichi Sayanagi, Toru Iwahashi, Koji Suzuki, Shunsuke Nishimoto, Kiyoshi Okada, Tsuyoshi Murase, Hideki Yoshikawa. Neurotropin® Accelerates the Differentiation of Schwann Cells and Remyelination in a Rat Lysophosphatidylcholine-Induced Demyelination Model. IJMS 2018;19:516
    https://doi.org/10.3390/ijms19020516