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1 "Jee Youn Lee"
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Original Article
Ghrelin Inhibits Oligodendrocyte Cell Death by Attenuating Microglial Activation
Jee Youn Lee, Tae Young Yune
Endocrinol Metab. 2014;29(3):371-378.   Published online September 25, 2014
DOI: https://doi.org/10.3803/EnM.2014.29.3.371
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  • 25 Web of Science
  • 23 Crossref
AbstractAbstract PDFPubReader   
Background

Recently, we reported the antiapoptotic effect of ghrelin in spinal cord injury-induced apoptotic cell death of oligodendrocytes. However, how ghrelin inhibits oligodendrocytes apoptosis, is still unknown. Therefore, in the present study, we examined whether ghrelin inhibits microglia activation and thereby inhibits oligodendrocyte apoptosis.

Methods

Using total cell extracts prepared from BV-2 cells activated by lipopolysaccharide (LPS) with or without ghrelin, the levels of p-p38 phosphor-p38 mitogen-activated protein kinase (p-p38MAPK), phospho-c-Jun N-terminal kinase (pJNK), p-c-Jun, and pro-nerve growth factor (proNGF) were examined by Western blot analysis. Reactive oxygen species (ROS) production was investigated by using dichlorodihydrofluorescein diacetate. To examine the effect of ghrelin on oligodendrocyte cell death, oligodendrocytes were cocultured in transwell chambers of 24-well plates with LPS-stimulated BV-2 cells. After 48 hours incubation, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and terminal deoxynucleotidyl transferase 2'-deoxyuridine, 5'-triphosphate nick end labeling staining were assessed.

Results

Ghrelin treatment significantly decreased levels of p-p38MAPK, p-JNK, p-c-Jun, and proNGF in LPS-stimulated BV-2 cells. ROS production increased in LPS-stimulated BV-2 cells was also significantly inhibited by ghrelin treatment. In addition, ghrelin significantly inhibited oligodendrocyte cell death when cocultured with LPS-stimulated BV-2 cells.

Conclusion

Ghrelin inhibits oligodendrocyte cell death by decreasing proNGF and ROS production as well as p38MAPK and JNK activation in activated microglia as an anti-inflammatory hormone.

Citations

Citations to this article as recorded by  
  • Ghrelin Represses Thymic Stromal Lymphopoietin Gene Expression through Activation of Glucocorticoid Receptor and Protein Kinase C Delta in Inflamed Skin Keratinocytes
    Hayan Jeong, Hyo-Jin Chong, Jangho So, Yejin Jo, Tae-Young Yune, Bong-Gun Ju
    International Journal of Molecular Sciences.2022; 23(7): 3977.     CrossRef
  • Inflammation: A Target for Treatment in Spinal Cord Injury
    Ximena Freyermuth-Trujillo, Julia J. Segura-Uribe, Hermelinda Salgado-Ceballos, Carlos E. Orozco-Barrios, Angélica Coyoy-Salgado
    Cells.2022; 11(17): 2692.     CrossRef
  • The Interplay between Ghrelin and Microglia in Neuroinflammation: Implications for Obesity and Neurodegenerative Diseases
    Cristina Russo, Maria Stella Valle, Antonella Russo, Lucia Malaguarnera
    International Journal of Molecular Sciences.2022; 23(21): 13432.     CrossRef
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  • Ghrelin-Mediated Regeneration and Plasticity After Nervous System Injury
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    Frontiers in Cell and Developmental Biology.2021;[Epub]     CrossRef
  • Microglial Lipid Biology in the Hypothalamic Regulation of Metabolic Homeostasis
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  • Acylated Ghrelin as a Multi-Targeted Therapy for Alzheimer's and Parkinson's Disease
    Niklas Reich, Christian Hölscher
    Frontiers in Neuroscience.2020;[Epub]     CrossRef
  • Effects of Ghrelin on the Apoptosis of Rheumatoid Arthritis Fibroblast-Like Synoviocyte MH7A Cells
    Junxian Ma, Xinbo Wang, Tingting Lv, Jie Liu, Ying Ren, Jinshan Zhang, Yan Zhang
    Biological and Pharmaceutical Bulletin.2019; 42(2): 158.     CrossRef
  • Direct and indirect effects of lipids on microglia function
    Q. Leyrolle, S. Layé, A. Nadjar
    Neuroscience Letters.2019; 708: 134348.     CrossRef
  • Dopamine neuronal protection in the mouse Substantia nigra by GHSR is independent of electric activity
    Bernardo Stutz, Carole Nasrallah, Mariana Nigro, Daniel Curry, Zhong-Wu Liu, Xiao-Bing Gao, John D. Elsworth, Liat Mintz, Tamas L. Horvath
    Molecular Metabolism.2019; 24: 120.     CrossRef
  • MK-0677, a Ghrelin Agonist, Alleviates Amyloid Beta-Related Pathology in 5XFAD Mice, an Animal Model of Alzheimer’s Disease
    Yu-on Jeong, Soo Shin, Jun Park, Bo Ku, Ji Song, Jwa-Jin Kim, Seong Jeon, Sang Lee, Minho Moon
    International Journal of Molecular Sciences.2018; 19(6): 1800.     CrossRef
  • Involvement of Astrocytes in Mediating the Central Effects of Ghrelin
    Laura Frago, Julie Chowen
    International Journal of Molecular Sciences.2017; 18(3): 536.     CrossRef
  • The neurological effects of ghrelin in brain diseases: Beyond metabolic functions
    Qian Jiao, Xixun Du, Yong Li, Bing Gong, Limin Shi, Tingting Tang, Hong Jiang
    Neuroscience & Biobehavioral Reviews.2017; 73: 98.     CrossRef
  • Neuropeptides and Microglial Activation in Inflammation, Pain, and Neurodegenerative Diseases
    Lila Carniglia, Delia Ramírez, Daniela Durand, Julieta Saba, Juan Turati, Carla Caruso, Teresa N. Scimonelli, Mercedes Lasaga
    Mediators of Inflammation.2017; 2017: 1.     CrossRef
  • Non-Neuronal Cells in the Hypothalamic Adaptation to Metabolic Signals
    Alejandra Freire-Regatillo, Pilar Argente-Arizón, Jesús Argente, Luis Miguel García-Segura, Julie A. Chowen
    Frontiers in Endocrinology.2017;[Epub]     CrossRef
  • The Ghrelin/GOAT System Regulates Obesity-Induced Inflammation in Male Mice
    Rebecca E. Harvey, Victor G. Howard, Moyra B. Lemus, Tara Jois, Zane B. Andrews, Mark W. Sleeman
    Endocrinology.2017; 158(7): 2179.     CrossRef
  • Central Modulation of Neuroinflammation by Neuropeptides and Energy-Sensing Hormones during Obesity
    Roger Maldonado-Ruiz, Lizeth Fuentes-Mera, Alberto Camacho
    BioMed Research International.2017; 2017: 1.     CrossRef
  • Lifestyle Shapes the Dialogue between Environment, Microglia, and Adult Neurogenesis
    Jorge Valero, Iñaki Paris, Amanda Sierra
    ACS Chemical Neuroscience.2016; 7(4): 442.     CrossRef
  • Signaling of ghrelin and its functional receptor, the growth hormone secretagogue receptor, promote tumor growth in glioblastomas
    Yousuke Okada, Yasuo Sugita, Koichi Ohshima, Motohiro Morioka, Satoru Komaki, Junko Miyoshi, Hideyuki Abe
    Neuropathology.2016; 36(6): 535.     CrossRef
  • Ghrelin-AMPK Signaling Mediates the Neuroprotective Effects of Calorie Restriction in Parkinson's Disease
    Jacqueline A. Bayliss, Moyra B. Lemus, Romana Stark, Vanessa V. Santos, Aiysha Thompson, Daniel J. Rees, Sandra Galic, John D. Elsworth, Bruce E. Kemp, Jeffrey S. Davies, Zane B. Andrews
    The Journal of Neuroscience.2016; 36(10): 3049.     CrossRef
  • MMP-3 secreted from endothelial cells of blood vessels after spinal cord injury activates microglia, leading to oligodendrocyte cell death
    Jee Y. Lee, Hae Y. Choi, Tae Y. Yune
    Neurobiology of Disease.2015; 82: 141.     CrossRef
  • Role of Non-Neuronal Cells in Body Weight and Appetite Control
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  • Articles in 'Endocrinology and Metabolism' in 2014
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