A predominantly glial origin of axonal ribosomes after nerve injury
Axonal mRNA transport and local protein synthesis are crucial for peripheral axon regeneration. To date, it remains unclear how ribosomes localize to axons. They may be co‐transported with mRNAs or, as suggested by recent studies, transferred from Schwann cells (SC). Here, we generated transgenic “R...
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Published in | Glia Vol. 66; no. 8; pp. 1591 - 1610 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.08.2018
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Subjects | |
Online Access | Get full text |
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Summary: | Axonal mRNA transport and local protein synthesis are crucial for peripheral axon regeneration. To date, it remains unclear how ribosomes localize to axons. They may be co‐transported with mRNAs or, as suggested by recent studies, transferred from Schwann cells (SC). Here, we generated transgenic “RiboTracker” mice expressing tdTomato‐tagged ribosomal protein L4 in specific cell types when crossed with Cre lines. Two neuronal RiboTracker‐Cre lines displayed extremely low levels of axonal L4‐tdTomato‐positive ribosomes. In contrast, two glial RiboTracker‐Cre lines revealed tagged ribosomes in sciatic nerve (SN) axons with increasing amounts after injury. Furthermore, non‐RiboTracker dorsal root ganglia co‐cultured with L4‐tdTomato‐expressing SCs displayed tagged ribosomes in axons. These data provide unequivocal evidence that SN axons receive ribosomes from SCs upon injury and indicate that glial cells are the main source of axonal ribosomes.
Main Points
The “RiboTracker” mouse allows in vivo tracking of the origin of axonal ribosomes.
Ribosomes are transferred from Schwann cells to axons in culture.
Sciatic nerve injury increases axonal localization of predominantly Schwann cell‐derived ribosomes. |
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Bibliography: | Funding information Kerstin Müller and Andrea Schnatz contributed equally to this work. Deutsche Forschungsgemeinschaft (DFG), Grant/Award Number: CRC TRR128; Focus Program Translational Neuroscience (FTN, Mainz); intramural funding from the JGU Mainz ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0894-1491 1098-1136 |
DOI: | 10.1002/glia.23327 |