Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Sci. Signal., 17 August 2010
Vol. 3, Issue 135, p. ec249
[DOI: 10.1126/scisignal.3135ec249]


Neuroscience More Than a Building Block

Elizabeth M. Adler

Science Signaling, AAAS, Washington, DC 20005, USA

The growth of neurites during the process of neuronal differentiation is associated with an increase in surface area that requires substantial membrane biosynthesis. Phosphatidylcholine (PtdCho), the major membrane phospholipid, can be synthesized from choline through a pathway in which choline is phosphorylated by choline kinase (CK), phosphocholine is converted to cytidine diphosphocholine (CDP-Cho) by CTP:phosphocholine cytidylyltransferase (CCT), and CDP-Cho is converted into PtdCho by CPT (CDP-choline:1,2-diacylglycerol cholinephosphotransferase). Marcucci et al. used radiolabeled choline together with lipid extraction to evaluate changes in the abundance of choline metabolites in Neuro-2a mouse neuroblastoma cells undergoing retinoic acid (RA)–induced neuronal differentiation. They found an initial increase in the abundance of CDP-Cho and PtdCho and only later (after 24 hours) saw an increase in the amounts of choline and phosphocholine. A combination of microarray analysis, real-time RT-qPCR, promoter-reporter assays, and analyses of the effects of inhibitors of RNA or protein synthesis indicated that the early increase in PtdCho production likely resulted from an increase in the activity of CCT{alpha}. This was followed by an increase in the stability of the mRNA encoding CK{alpha} and then by the transcriptional activation of the genes encoding both CK{alpha} and CCT{alpha}. Clonal cell lines with stable expression of constitutively active CK{alpha} or CCT{alpha} showed increased PtdCho production in the absence of RA along with an increase in neurite formation. Moreover, they showed an increase in the abundance of βIII-tubulin, a neurite marker, and in the expression of various neuronal genes. RA stimulated the phosphorylation of extracellular signal–regulated kinase (ERK), whereas pharmacological inhibition of the ERK signaling pathway blocked the RA-dependent transcriptional activation of the genes encoding CK{alpha} and CCT{alpha}, the increase in PtdCho biosynthesis, and the stimulation of neurite outgrowth. ERK phosphorylation was also increased in the cell lines expressing constitutively active CK{alpha} or CCT{alpha}. The authors conclude that enhanced PtdCho biosynthesis, which is stimulated by RA, can itself promote neurite formation and neuronal differentiation.

H. Marcucci, L. Paoletti, S. Jackowski, C. Banchio, Phosphatidylcholine biosynthesis during neuronal differentiation and its role in cell fate determination. J. Biol. Chem. 285, 25382–25393 (2010). [Abstract] [Full Text]

Citation: E. M. Adler, More Than a Building Block. Sci. Signal. 3, ec249 (2010).

To Advertise     Find Products

Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882