| Literature DB >> 29199072 |
Bojana Zupan1, Bingfang Liu2, Faten Taki2, Judit Gal Toth2, Miklos Toth3.
Abstract
Tumor necrosis factor alpha (TNF-α) is a cytokine that not only coordinates local and systemic immune responses [1, 2] but also regulates neuronal functions. Most prominently, glia-derived TNF-α has been shown to regulate homeostatic synaptic scaling [3-6], but TNF-α-null mice exhibited no apparent cognitive or emotional abnormalities. Instead, we found a TNF-α-dependent intergenerational effect, as mothers with a deficit in TNF-α programmed their offspring to exhibit low innate fear. Cross-fostering and conditional knockout experiments indicated that a TNF-α deficit in the maternal brain, rather than in the hematopoietic system, and during gestation was responsible for the low-fear offspring phenotype. The level of innate fear governs the balance between exploration/foraging and avoidance of predators and is thus fundamentally important in adaptation, fitness, and survival [7]. Because maternal exercise and activity are known to reduce both brain TNF-α [8] and offspring innate fear [9], whereas maternal stress has been reported to increase brain TNF-α [10] and offspring fear and anxiety [11, 12], maternal brain TNF-α may report environmental conditions to promote offspring behavioral adaptation to their anticipated postnatal environment.Entities:
Keywords: TNF; anxiety; behavioral adaptation; conditional knockout; cross-fostering; evolution; fear; maternal effect; maternal programming
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Year: 2017 PMID: 29199072 PMCID: PMC6170164 DOI: 10.1016/j.cub.2017.10.071
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834