학술논문

The Golgi Outpost Protein TPPP Nucleates Microtubules and Is Critical for Myelination
Document Type
article
Source
Cell. 179(1)
Subject
Biochemistry and Cell Biology
Biological Sciences
Brain Disorders
Neurosciences
Underpinning research
1.1 Normal biological development and functioning
Animals
Animals
Newborn
Axons
Carrier Proteins
Cell-Free System
Cells
Cultured
Escherichia coli
Gene Knockdown Techniques
Golgi Apparatus
Humans
Mice
Mice
Inbred C57BL
Mice
Knockout
Microtubule-Organizing Center
Microtubules
Myelin Sheath
Nerve Tissue Proteins
Oligodendrocyte Precursor Cells
Rats
Rats
Sprague-Dawley
Tubulin
Golgi outpost
TPPP
branching
mass spectrometry
microtubule
myelin
nucleation
oligodendrocyte
Medical and Health Sciences
Developmental Biology
Biological sciences
Biomedical and clinical sciences
Language
Abstract
Oligodendrocytes extend elaborate microtubule arbors that contact up to 50 axon segments per cell, then spiral around myelin sheaths, penetrating from outer to inner layers. However, how they establish this complex cytoarchitecture is unclear. Here, we show that oligodendrocytes contain Golgi outposts, an organelle that can function as an acentrosomal microtubule-organizing center (MTOC). We identify a specific marker for Golgi outposts-TPPP (tubulin polymerization promoting protein)-that we use to purify this organelle and characterize its proteome. In in vitro cell-free assays, recombinant TPPP nucleates microtubules. Primary oligodendrocytes from Tppp knockout (KO) mice have aberrant microtubule branching, mixed microtubule polarity, and shorter myelin sheaths when cultured on 3-dimensional (3D) microfibers. Tppp KO mice exhibit hypomyelination with shorter, thinner myelin sheaths and motor coordination deficits. Together, our data demonstrate that microtubule nucleation outside the cell body at Golgi outposts by TPPP is critical for elongation of the myelin sheath.