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Melatonin increases proliferation of cultured neural stem cells obtained from adult mouse subventricular zone
Author(s) -
Sotthibundhu Areechun,
PhansuwanPujito Pansiri,
Govitrapong Piyarat
Publication year - 2010
Publication title -
journal of pineal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 131
eISSN - 1600-079X
pISSN - 0742-3098
DOI - 10.1111/j.1600-079x.2010.00794.x
Subject(s) - melatonin , subventricular zone , luzindole , neurogenesis , biology , neural stem cell , endocrinology , medicine , stem cell , microbiology and biotechnology , pineal gland , pinealocyte , melatonin receptor , receptor , biochemistry
Melatonin, a circadian rhythm–promoting molecule secreted mainly by the pineal gland, has a variety of biological functions and neuroprotective effects including control of sleep–wake cycle, seasonal reproduction, and body temperature as well as preventing neuronal cell death induced by neurotoxic substances. Melatonin also modulates neural stem cell (NSC) function including proliferation and differentiation in embryonic brain tissue. However, the involvement of melatonin in adult neurogenesis is still not clear. Here, we report that precursor cells from adult mouse subventricular zone (SVZ) of the lateral ventricle, the main neurogenic area of the adult brain, express melatonin receptors. In addition, precursor cells derived from this area treated with melatonin exhibited increased proliferative activity. However, when cells were treated with luzindole, a competitive inhibitor of melatonin receptors, or pertussis toxin, an uncoupler of Gi from adenylate cyclase, melatonin‐induced proliferation was reduced. Under these conditions, melatonin induced the differentiation of precursor cells to neuronal cells without an upregulation of the number of glia cells. Because stem cell replacement is thought to play an important therapeutic role in neurodegenerative diseases, melatonin might be beneficial for stimulating endogenous neural stem cells.