[Myelinosomes: A new pathway of protein quality control].

Med Sci (Paris)

Laboratoire STIM, Équipe 4CS, ERL CNRS 7003. 1 rue Georges Bonnet 86022 Poitiers Cedex, France - CHU de Poitiers, Poitiers F-86021, France.

Published: November 2020

AI Article Synopsis

  • Maintenance of cell proteostasis involves two main pathways: the proteasome and autophagy, which typically aim to degrade abnormal proteins.
  • A new mechanism has been identified that prevents the degradation of these abnormal proteins by packaging them into nanovesicles called myelinosomes, which are released from the cell.
  • Myelinosomes are formed under stressful conditions or due to genetic factors and play a crucial role in removing dysfunctional proteins in diseases like Huntington's and cystic fibrosis, thus helping to maintain cellular health.

Article Abstract

Maintenance of cell proteostasis relies on two degradation pathways: proteasome and autophagy. Here we describe a new proteostasis pathway avoiding degradation of abnormal proteins yet carrying them outside the cell using nanovesicles called myelinosomes. These myelinosomes are produced in pathological or stress situations in relation with genetic or environmental factors. Myelinosome vesicles are nano-sized multi-stacked membrane structures, resembling myelin sheath. It has recently been shown in two models of genetic diseases (Huntington's disease and cystic fibrosis) that myelinosomes are important for eliminating mutant proteins in an unusual secretory process, thus preventing their accumulation and aggregation in cells.

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http://dx.doi.org/10.1051/medsci/2020173DOI Listing

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[Myelinosomes: A new pathway of protein quality control].

Med Sci (Paris)

November 2020

Laboratoire STIM, Équipe 4CS, ERL CNRS 7003. 1 rue Georges Bonnet 86022 Poitiers Cedex, France - CHU de Poitiers, Poitiers F-86021, France.

Article Synopsis
  • Maintenance of cell proteostasis involves two main pathways: the proteasome and autophagy, which typically aim to degrade abnormal proteins.
  • A new mechanism has been identified that prevents the degradation of these abnormal proteins by packaging them into nanovesicles called myelinosomes, which are released from the cell.
  • Myelinosomes are formed under stressful conditions or due to genetic factors and play a crucial role in removing dysfunctional proteins in diseases like Huntington's and cystic fibrosis, thus helping to maintain cellular health.
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Objective: To define the composition of cytoplasmic inclusions forming stacks and concentric whorls in histiocytes and mesothelial cells of serous fluids, imparting to them a resemblance to Gaucher cells, and to draw conclusions on the mechanism of their formation.

Study Design: Three serous fluids (one pleural and two pericardial) containing a fair number of the cells referred to were progressively subjected to the following studies: (1) cytochemistry for mucopolysaccharides, proteins, phospholipids and hemoglobin; (2) immunocytochemistry for immunoglobulins IgA, IgG, IgM and lysozyme; (3) transmission electron microscopy (TEM), and (4) scanning electron microscopy-based energy dispersive X-ray microanalysis (SEM-EDAX).

Results: All three specimens were blood stained and contained large numbers of histiocytes and mesothelial cells, arranged singly and in groups, with abundant cytoplasmic inclusions.

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