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Morante-Redolat, J. M.

Publications and source records attributed to Morante-Redolat, J. M..

2 recordsLinked to original sources

AimSeg: a machine-learning-aided tool for axon, inner tongue and myelin segmentation

Electron microscopy (EM) images of axons and their ensheathing myelin from both the central and peripheral nervous system are used for assessing myelin formation, degeneration (demyelination) and regeneration (remyelination). The g-ratio is the gold standard measure of assessing myelin thickness and quality, and traditionally is determined from measurements done manually from EM images - a time-consuming endeavour with limited reproducibility. These measurements have also historically neglected the innermost uncompacted myelin sheath, known as the inner myelin tongue. Nonetheless, the inner tongue has been shown to be important for myelin growth and some studies have reported that certain conditions can elicit its enlargement. Ignoring this fact may bias the standard g-ratio analysis, whereas quantifying the uncompacted myelin has the potential to provide novel insights in the myelin field. In this regard, we have developed AimSeg, a bioimage analysis tool for axon, inner tongue and myelin segmentation. Aided by machine learning classifiers trained on tissue undergoing remyelination, AimSeg can be used either as an automated workflow or as a user-assisted segmentation tool. Validation results show good performance segmenting all three fibre components, with the assisted segmentation showing the potential for further improvement with minimal user intervention. This results in a considerable reduction in time for analysis compared with manual annotation. AimSeg could also be used to build larger, high quality ground truth datasets to train novel deep learning models. Implemented in Fiji, AimSeg can use machine learning classifiers trained in ilastik. This, combined with a user-friendly interface and the ability to quantify uncompacted myelin, makes AimSeg a unique tool to assess myelin growth. Author SummaryMyelin is formed by specialised cells that wrap themselves around axons and has a major role in the function, protection, and maintenance of nerves. These functions are disturbed by demyelinating diseases, such as multiple sclerosis. In this work we present AimSeg, a new tool based on artificial intelligence algorithms (machine learning) to assess myelin growth on electron microscopy images. Whereas standard metrics and previous computational methods focus on quantifying compact myelin, AimSeg also quantifies the inner myelin tongue (uncompacted myelin). This structure has been largely overlooked despite the fact that it has an important role in the process of myelin growth (both during development and in the adult brain) and recent studies have reported morphological changes associated with some diseases. We report the performance of AimSeg, both as a fully automated approach and in an assisted segmentation workflow that enables the user to curate the results on-the-fly while reducing human intervention to the minimum. Therefore, AimSeg stands as a novel bioimage analysis tool that meets the challenges of assessing myelin growth by supporting both standard metrics for myelin evaluation and the quantification of the uncompacted myelin in different conditions.

bioinformatics↗

The rates of adult neurogenesis and oligodendrogenesis are linked to cell cycle regulation through p27-dependent gene repression of SOX2

Cell differentiation involves profound changes in global gene expression that often have to occur in coordination with cell cycle exit. Because cyclin-dependent kinase inhibitor p27 reportedly regulates proliferation of neural progenitor cells in the subependymal neurogenic niche of the adult mouse brain, but can also have effects on gene expression, we decided to molecularly analyze its role in adult neurogenesis and oligodendrogenesis. At the cell level, we show that p27 restricts residual cyclin-dependent kinase activity after mitogen withdrawal to antagonize cycling, but it is not essential for cell cycle exit. Contrasting gene expression with chromatin accessibility, we find that p27 is coincidentally necessary to globally repress many genes involved in the transit from multipotentiality to differentiation, including those coding for neural progenitor transcription factors SOX2, OLIG2, and ASCL1. Our data reveal both direct association of p27 with regulatory sequences in the three genes and an additional hierarchical relationship where p27 repression of the Sox2 gene leads to reduced levels of SOX2-downstream targets Olig2 and Ascl1. In vivo, p27 is also required for the regulation of the proper level of SOX2 necessary for neuroblasts and oligodendroglial progenitor cells to timely exit cell cycle in a lineage-dependent manner.

neuroscience↗