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Biology subjects

Renner, A.

Publications and source records attributed to Renner, A..

2 recordsLinked to original sources

Head-Direction Cells in Postsubiculum Show Systematic Parallax Errors During Visual Anchoring

The rodent head-direction (HD) system provides an allocentric orientation signal for spatial navigation through integration of self-motion inputs and visual landmarks ( cues). Inferring HD from nearby visual cues faces a fundamental challenge: the direction towards the cue shifts with the animals position. If left uncorrected, this introduces a position-dependent parallax error. Here, we show that the HD signal in freely moving mice indeed exhibits a position-dependent bias consistent with parallax in a single-cue environment. This bias is smaller than predicted by geometric parallax and is further reduced in more natural multi-cue settings. Computational modeling revealed that this reduction of parallactic error can be explained by two averaging operations: multi-view averaging - temporal integration of the same cue viewed from different locations, and multi-cue averaging - concurrent weighting of multiple cues. Thus, averaging without explicit position-dependent correction provides a fast and robust heuristic that the HD system seems to employ for the maintenance of the internal compass. Our findings have broader implications for biological and artificial navigation systems. First, accurate allocentric reference frames are a key component of the cognitive map postulated in the extended hippocampal circuit and used for spatial cognition as well as abstract mental manipulation. Second, the employment of a fast heuristic in the HD system echoes heuristic strategies observed in other behaviors, such as decision making. More broadly, these findings highlight a trade-off in neural coding between computational efficiency and positional accuracy.

neuroscience↗

The biotoxin BMAA promotes mesenchymal transition in neuroblastoma cells

Mesenchymal-like cancer cells are an indicator of malignant tumors as they exhibit tumorigenic properties including downregulation of differentiation markers, and increased colony-forming potential, motility, and chemoresistance. We have previously demonstrated that the cyanobacterial biotoxin beta-methylamino-L-alanine (BMAA) is capable of influencing neural cell differentiation state through mechanisms involving the Wnt signaling pathway, suggesting the possibility that BMAA may play a role in influencing other Wnt related differentiation processes including mesenchymal transition. In this study we present evidence characterizing the effects of BMAA on mesenchymal transition in a human neuroblastoma cell line and provide support for the hypothesis that the biotoxin can promote this process in these cells by altering differentiation state, inducing changes in gene expression, and changing cellular function in manners consistent with cellular mesenchymal transition. Results of this study indicate that BMAA exposure may promote carcinogenesis through its effects on cell differentiation state in certain contexts. These results suggest that exposure to the biotoxin BMAA may be an influencing factor in chemotherapy resistance and cancer relapse in neuroblastoma.

molecular biology↗