Omega-3 polyunsaturated Fatty acids enhance neuronal differentiation in cultured rat neural stem cells.

Polyunsaturated fatty acids (PUFAs) can induce neurogenesis and recovery from brain diseases. However, the exact mechanisms of the beneficial effects of PUFAs have not been conclusively described. We recently reported that docosahexaenoic acid (DHA) induced neuronal differentiation by decreasing Hes1 expression and increasing p27(kip1) expression, which causes cell cycle arrest in neural stem cells (NSCs). In the present study, we examined the effect of eicosapentaenoic acid (EPA) and arachidonic acid (AA) on differentiation, expression of basic helix-loop-helix transcription factors (Hes1, Hes6, and NeuroD), and the cell cycle of cultured NSCs. EPA also increased mRNA levels of Hes1, an inhibitor of neuronal differentiation, Hes6, an inhibitor of Hes1, NeuroD, and Map2 mRNA and Tuj-1-positive cells (a neuronal marker), indicating that EPA induced neuronal differentiation. EPA increased the mRNA levels of p21(cip1) and p27(kip1), a cyclin-dependent kinase inhibitor, which indicated that EPA induced cell cycle arrest. Treatment with AA decreased Hes1 mRNA but did not affect NeuroD and Map2 mRNA levels. Furthermore, AA did not affect the number of Tuj-1-positive cells or cell cycle progression. These results indicated that EPA could be involved in neuronal differentiation by mechanisms alternative to those of DHA, whereas AA did not affect neuronal differentiation in NSCs.

Cis-9,trans-11-conjugated linoleic acid promotes neuronal differentiation through regulation of Hes6 mRNA and cell cycle in cultured neural stem cells.

Conjugated linoleic acids (CLAs) are positional and geometrical isomers of linoleic acid (LA). Cis-9,trans-11-CLA (CLA), the main isomer of CLAs in foods derived from ruminants, has several beneficial effects for humans and animals; however, its effects on the central nervous system are largely unknown. In this study, we investigated the effects of LA and CLA on neuronal differentiation of neural stem cells (NSCs). NSCs cultured with or without LA and CLA were assessed by immunofluorescence staining, mRNA measurement of basic helix-loop-helix transcription factors and cyclin-dependent kinase inhibitors by real-time PCR, BrdU incorporation analysis and flow cytometry analysis. In NSCs treated with CLA, the number of Tuj-1-positive cells (neurons) and the mRNA expression levels of Hes6, MAP2, p21(cip1) and p27(kip1) increased, while the proportion of S-phase cells decreased; compared with the control, no change was demonstrated in NSCs treated with LA. These results suggest that CLA promotes neuronal differentiation by increasing, in part, the expression of Hes6 mRNA and by activating p21(cip1) and p27(kip1) to arrest cell cycle.