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Preparation of Rat Oligodendrocyte Progenitor Cultures and Quantification of Oligodendrogenesis Using Dual-infrared Fluorescence Scanning
Published on: February 17, 2016
Myelin basic protein functions as a microtubule stabilizing protein in differentiated oligodendrocytes
M R Galiano1, A Andrieux, J C Deloulme
1CIQUIBIC-Dpto. Química Biológica, Facultad Ciencias Químicas, Haya de la Torre S/N, Córdoba, Argentina.
Abstract:
Myelin basic protein (MBP) is an oligodendrocyte-specific protein essential for oligodendrocyte morphogenesis at late stages of cell differentiation. There is evidence that the morphogenetic function of MBP is mediated by MBP interaction with the cytoskeleton. Thus, an MBP/cytoplasmic microtubule association has been reported, and MBP has Ca(2+)/calmodulin-regulated microtubule cold-stabilizing activity in vitro. However, the unambiguous demonstration of a microtubule-stabilizing activity for MBP in cells has been difficult because oligodendrocytes contain variants of STOP (stable tubule only polypeptide) proteins, which are responsible for microtubule cold stability in different cell types. Herein, we have used genetic mouse models and RNA interference to assay independently the microtubule cold-stabilizing activities of MBP and of STOP in developing oligodendrocytes. In wild-type oligodendrocytes, microtubules were cold stable throughout maturation, which is consistent with the presence of STOP proteins from early stages of differentiation. In contrast, in oligodendrocytes from STOP-deficient mice, microtubules were cold labile in the absence of MBP expression or when MBP expression was restricted to the cell body and became stable in fully differentiated oligodendrocytes, where MBP is expressed in cell extensions. The suppression of MBP by RNA interference in STOP-deficient oligodendrocytes suppressed microtubule cold stability. Additionally, STOP suppression in oligodendrocytes derived from shiverer mice that lack MBP led to the complete suppression of microtubule cold stability at all stages of cell differentiation. These results demonstrate that both STOP and MBP function as microtubule-stabilizing proteins in differentiating oligodendrocytes and could be important for the morphogenetic function of MBP.
Insights
Myelin basic protein (MBP) and stable tubule only polypeptide (STOP) proteins stabilize microtubules in developing oligodendrocytes. This dual stabilization is crucial for oligodendrocyte morphogenesis and cell differentiation.
Area of Science:
- Neuroscience
- Cell Biology
- Molecular Biology
Background:
- Myelin basic protein (MBP) is vital for oligodendrocyte morphogenesis, potentially via cytoskeleton interaction.
- Microtubule cold-stabilizing activity of MBP has been observed in vitro but difficult to demonstrate in cells.
- Oligodendrocytes express stable tubule only polypeptide (STOP) proteins, which also affect microtubule stability.
Purpose of the Study:
- To independently assess the microtubule cold-stabilizing activities of MBP and STOP in developing oligodendrocytes.
- To elucidate the roles of MBP and STOP in oligodendrocyte differentiation and morphogenesis.
Main Methods:
- Utilized genetic mouse models (STOP-deficient and shiverer mice lacking MBP).
- Employed RNA interference (RNAi) to suppress MBP and STOP expression.
- Assessed microtubule cold stability in oligodendrocytes at different differentiation stages.
Main Results:
- Microtubules were cold stable in wild-type oligodendrocytes throughout maturation.
- In STOP-deficient oligodendrocytes, microtubules were cold labile without MBP or with cell-body restricted MBP, becoming stable upon MBP expression in cell extensions.
- MBP suppression in STOP-deficient oligodendrocytes reduced microtubule stability.
- STOP suppression in MBP-deficient (shiverer) oligodendrocytes abolished microtubule cold stability at all stages.
Conclusions:
- Both STOP and MBP function as critical microtubule-stabilizing proteins in differentiating oligodendrocytes.
- The combined action of STOP and MBP is essential for microtubule cold stability and likely contributes to MBP's morphogenetic function.
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