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Martinez-Garcia, F.

Publications and source records attributed to Martinez-Garcia, F..

2 recordsLinked to original sources

Doublecortin-immunoreactive immature neurons in the olfactory system across pregnancy and lactation in female mice

Motherhood is a critical period modulating behavioural changes to favour survival in mammals. In mice, olfaction is a key driver of social behaviours, and adult neurogenesis in the olfactory bulb is modulated at this stage, contributing to pup recognition. However, whether motherhood would also promote changes in the population of immature neurons of the piriform cortex is unknown. To investigate this question, we analysed the expression of doublecortin (DCX), a marker of immature neurons, in prepubescent vs young adults, in virgin vs pregnant and in pup-sensitized virgins vs lactating female mice. We found that the density of DCX cells sharply decreased in the piriform cortex with age, but pregnancy and lactation failed to significantly alter the density of these cells. To further analyse how motherhood could affect DCX-ir cells, we co-labelled DCX cells with NeuN, an archetypical marker of mature neurons. We did not find significant differences in the percentage of double-labelled cells nor in features related to maturation like number of neurites or main diameter in lactating dams as compared to pup-sensitized virgin females. Our results suggest that the first pregnancy does not significantly affect the differentiation of immature neurons of the piriform cortex.

neuroscience↗

Proteomic characterization of GSK3β knockout shows altered cell adhesion and metabolic pathway utilisation in colorectal cancer cells

Glycogen-specific kinase (GSK3{beta}) is an integral regulator of the Wnt signalling pathway as well as many other diverse signalling pathways and processes. Dys-regulation of GSK3{beta} is implicated in many different pathologies, including neurodegenerative disorders as well as many different tumour types. In the context of tumour development, GSK3{beta} has been shown to play both oncogenic and tumour suppressor roles, depending upon tissue, signalling environment or disease progression. Although multiple substrates of the GSK3{beta} kinase have been identified, the wider protein networks within which GSK3{beta} participates are not well known, and the consequences of these interactions not well understood. In this study, LC-MS/MS expression analysis was performed using knockout GSK3{beta} colorectal cancer cells and isogenic controls in colorectal cancer cell lines carrying dominant stabilizing mutations of {beta}-Catenin. Consistent with the role GSK3{beta}, we found that {beta}-Catenin levels and canonical Wnt activity are unaffected by knockout of GSK3{beta} and therefore use this knockout cell model to identify other processes in which GSK3{beta} is implicated. Quantitative proteomic analysis revealed perturbation of proteins involved in cell-cell adhesion, and we characterize the phenotype and altered proteomic profiles associated with this. We also characterize the perturbation of metabolic pathways resulting from GSK3{beta} knockout and identify defects in glycogen metabolism. In summary, using a precision colorectal cancer cell-line knockout model with constitutively activated {beta}-Catenin we are able to identify several of the diverse pathways and processes associated with GSK3{beta} function.

cancer biology↗