Lactoferrin Modulates Induction of Transcription Factor c-Fos in Neuronal Cultures.
Marina Yu KopaevaAsya M AzievaAnton B CherepovIrina Yu ZarayskayaPublished in: International journal of molecular sciences (2023)
Lactoferrin (Lf) is a multifunctional protein from the transferrin family. Of particular interest is the ability of Lf to affect a wide range of neuronal processes by modulating the expression of genes involved in long-term neuroplasticity. The expression of the immediate early gene c-fos that is rapidly activated in response to external influences, and its product, transcription factor c-Fos, is widely used as a marker of long-term neuronal plasticity. The present study aims to examine the effect of human Lf on the induction of transcription factor c-Fos in the primary mouse neuronal cultures after stimulation and to determine the cellular localization of human Lf and its colocalization with induced c-Fos protein. Primary dissociated cultures of hippocampal cells were obtained from the brains of newborn C57BL/6 mice (P0-P1). On day 7 of culturing, human Lf was added to the medium. After 24 h (day 8 in culture), c-Fos protein was induced in cells by triple application of 50 mM KCl. c-Fos content was analyzed using the immunofluorescent method 2 h after stimulation. Stimulation promoted exogenous Lf translocation into the nuclei of cultured neuronal cells, which correlated with increased induction of transcription factor c-Fos and was accompanied by nuclear colocalization of these proteins. These results attest to the potential of Lf as a modulator of neuronal processes and open up new prospects in studying the mechanisms of the regulatory effects of lactoferrin on cell function.
Keyphrases
- transcription factor
- endothelial cells
- induced apoptosis
- cerebral ischemia
- cell cycle arrest
- high glucose
- dna binding
- poor prognosis
- binding protein
- pluripotent stem cells
- signaling pathway
- induced pluripotent stem cells
- gene expression
- blood brain barrier
- climate change
- cell death
- dna methylation
- drug delivery
- brain injury
- risk assessment
- genome wide
- drug induced
- cell proliferation