Hyperactivation of BDNF-TrkB signaling cascades in human hypothalamic hamartoma (HH): A potential mechanism contributing to epileptogenesis

Suzan Semaan, Jie Wu, Yan Gan, Yu Jin, Guo Hui Li, John F. Kerrigan, Yong Chang Chang, Yao Huang

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Aims: Although compelling evidence suggests that human hypothalamic hamartoma (HH) is intrinsically epileptogenic for gelastic seizures, the molecular mechanisms responsible for epileptogenesis within HH remain to be elucidated. The aim of this study was to test the hypothesis that hyperactivation of BDNF-TrkB signaling pathways in surgically resected HH tissue is a possible mechanism for downregulation of KCC2 expression, which in turn underlies GABA-mediated excitation within HH. Methods: Activation of three major BDNF-TrkB signaling pathways including MAPKs, Akt, and PLCγ1 were evaluated in surgically resected HH tissue (n = 14) versus human hypothalamic control tissue (n = 8) using combined methodologies of biochemistry, molecular biology, cell biology, and electrophysiology. Results: Our data show that compared with hypothalamic control tissue, in HH tissue, (i) activation of TrkB and expression of mature BDNF are elevated; (ii) MAPKs (including ERK1/2, p38, and JNK), Akt, and PLCγ1 are highly activated; (iii) KCC2 expression is downregulated; and (iv) pharmacological manipulation of TrkB signaling alters HH neuronal firing rate. Conclusion: Our findings suggest that multiple BDNF-TrkB signaling pathways are activated in HH. They act independently or collaboratively to downregulate KCC2 expression, which is the key component for GABA-mediated excitation associated with gelastic seizures.

Original languageEnglish (US)
Pages (from-to)164-172
Number of pages9
JournalCNS Neuroscience and Therapeutics
Volume21
Issue number2
DOIs
StatePublished - Feb 1 2015
Externally publishedYes

Keywords

  • Brain-derived neurotrophic factor
  • Epileptogenesis
  • Human hypothalamic hamartoma
  • Signal transduction
  • Tropomysin-related kinase B

ASJC Scopus subject areas

  • Pharmacology
  • Psychiatry and Mental health
  • Physiology (medical)
  • Pharmacology (medical)

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