Peripheral mRNA expression of pluripotency markers in bipolar disorder and the effect of long-term lithium treatment

• Published in: Pharmacological reports Vol. 68; no. 5; pp. 1042 - 1045
• Main Authors: Ferensztajn-Rochowiak, Ewa, Tarnowski, Maciej, Samochowiec, Jerzy, Michalak, Michal, Ratajczak, Mariusz Z., Rybakowski, Janusz K.
• Format: Journal Article
• Language: English
• Published: Cham Elsevier Urban & Partner Sp. z o.o 01.10.2016; Springer International Publishing
• Subjects: Biomarkers - metabolism; bipolar disorder; Bipolar Disorder - drug therapy; Bipolar Disorder - metabolism; CD3 Complex - metabolism; Drug Safety and Pharmacovigilance; Embryonic Stem Cells - drug effects; Embryonic Stem Cells - metabolism; Female; Humans; lithium; Lithium - therapeutic use; Male; Middle Aged; Nanog; Nanog Homeobox Protein - metabolism; Oct-4; Octamer Transcription Factor-3 - metabolism; Pharmacotherapy; Pharmacy; RNA, Messenger - metabolism; Short Communication; Sox 2; SOXB1 Transcription Factors - metabolism; Oct-4; lithium; bipolar disorder; Sox 2; Nanog
• ISSN: 1734-1140; 2299-5684; 2299-5684
• DOI: 10.1016/j.pharep.2016.06.006

The aim was to evaluate the peripheral mRNA expression of pluripotency master transcriptional factors such as octamer-binding transcription factor 4 (Oct4), sex-determining region Y-box 2 (Sox2) and homeobox protein Nanog, in patients with bipolar disorder (BD), and the effect of long-term lithium treatment. Fifteen BD patients (aged 53±7years) not treated with lithium, with duration of illness>10years, 15 BD patients (aged 55±6years) treated with lithium for 8–40 years (mean 16years) and 15 control subjects (aged 50±5years) were included. Assessment of the mRNA levels of pluripotency markers (Oct-4, Sox 2 and Nanog) was performed, using the Real-time quantitative reverse transcription PCR (RQ-PCR) procedure, and the number of CD34+ very small embryonic-like stem cells (VSELs) was measured by flow cytometric analysis. In those BD patients not treated with lithium the expression of all three pluripotency genes was significantly higher than that in the control subjects. Oct-4, Sox2 and Nanog also positively correlated with the number of CD34+ VSELs/[ul] in this group. In the lithium-treated patients the mRNA levels of Nanog were significantly higher than in the control individuals and correlated with the number and % of CD34+ VSELs. The overexpression of the pluripotency master transcriptional factors in patients with a long duration of BD not treated with lithium, may contribute to the pathogenesis of the illness and make them potential biological markers of BD. Long-term lithium treatment may attenuate these excessive regenerative processes, especially in relation to the transcription factors Oct-4 and Sox2.