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Differential responses to lithium in hyperexcitable neurons from patients with bipolar disorder

  • Jerome Mertens
  • , Qiu Wen Wang
  • , Yongsung Kim
  • , Diana X. Yu
  • , Son Pham
  • , Bo Yang
  • , Yi Zheng
  • , Kenneth E. Diffenderfer
  • , Jian Zhang
  • , Sheila Soltani
  • , Tameji Eames
  • , Simon T. Schafer
  • , Leah Boyer
  • , Maria C. Marchetto
  • , John I. Nurnberger
  • , Joseph R. Calabrese
  • , Ketil J. Ødegaard
  • , Michael J. McCarthy
  • , Peter P. Zandi
  • , Martin Alba
  • Caroline M. Nievergelt, Shuangli Mi, Kristen J. Brennand, John R. Kelsoe, Fred H. Gage, Jun Yao
  • Tsinghua University
  • Salk Institute for Biological Studies
  • Beijing Institute of Genomics Chinese Academy of Sciences (China National Center for Bioinformation)
  • Indiana U. Purdue U. (IUPUI)
  • Case Western Reserve University
  • University of Bergen
  • Veterans Affairs San Diego Healthcare System San Diego
  • Department of Psychiatry
  • Johns Hopkins School of Medicine
  • Dalhousie University, Faculty of Medicine
  • Mount Sinai School of Medicine
  • Jiangsu Normal University

Research output: Contribution to journalArticlepeer-review

460 Scopus citations

Abstract

Bipolar disorder is a complex neuropsychiatric disorder that is characterized by intermittent episodes of mania and depression; without treatment, 15% of patients commit suicide. Hence, it has been ranked by the World Health Organization as a top disorder of morbidity and lost productivity. Previous neuropathological studies have revealed a series of alterations in the brains of patients with bipolar disorder or animal models, such as reduced glial cell number in the prefrontal cortex of patients, upregulated activities of the protein kinase A and C pathways and changes in neurotransmission. However, the roles and causation of these changes in bipolar disorder have been too complex to exactly determine the pathology of the disease. Furthermore, although some patients show remarkable improvement with lithium treatment for yet unknown reasons, others are refractory to lithium treatment. Therefore, developing an accurate and powerful biological model for bipolar disorder has been a challenge. The introduction of induced pluripotent stem-cell (iPSC) technology has provided a new approach. Here we have developed an iPSC model for human bipolar disorder and investigated the cellular phenotypes of hippocampal dentate gyrus-like neurons derived from iPSCs of patients with bipolar disorder. Guided by RNA sequencing expression profiling, we have detected mitochondrial abnormalities in young neurons from patients with bipolar disorder by using mitochondrial assays; in addition, using both patch-clamp recording and somatic Ca 2+ imaging, we have observed hyperactive action-potential firing. This hyperexcitability phenotype of young neurons in bipolar disorder was selectively reversed by lithium treatment only in neurons derived from patients who also responded to lithium treatment. Therefore, hyperexcitability is one early endophenotype of bipolar disorder, and our model of iPSCs in this disease might be useful in developing new therapies and drugs aimed at its clinical treatment.

Original languageEnglish
Pages (from-to)95-99
Number of pages5
JournalNature
Volume527
Issue number7576
DOIs
StatePublished - 5 Nov 2015
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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