Astrocyte-derived tissue Transglutaminase affects fibronectin deposition, but not aggregation, during cuprizone-induced demyelinationEspitia Pinzon, N., Sanz-Morello, B., Breve, J. J. P., Bol, J. G. J. M., Drukarch, B., Bauer, J., Baron, W. & van Dam, A-M., 27-Jan-2017, In : Scientific Reports. 7, 13 p., 40995.
Research output: Contribution to journal › Article › Academic › peer-review
Astrogliosis as seen in Multiple Sclerosis (MS) develops into astroglial scarring, which is beneficial because it seals off the site of central nervous system (CNS) damage. However, astroglial scarring also forms an obstacle that inhibits axon outgrowth and (re) myelination in brain lesions. This is possibly an important cause for incomplete remyelination in the CNS of early stage MS patients and for failure in remyelination when the disease progresses. In this study we address whether under demyelinating conditions in vivo, tissue Transglutaminase (TG2), a Ca2+-dependent enzyme that catalyses posttranslational modification of proteins, contributes to extracellular matrix (ECM) deposition and/or aggregation. We used the cuprizone model for de- and remyelination. TG2 immunoreactivity and enzymatic activity time-dependently appeared in astrocytes and ECM, respectively, in the corpus callosum of cuprizone-treated mice. Enhanced presence of soluble monomeric and multimeric fibronectin was detected during demyelination, and fibronectin immunoreactivity was slightly decreased in cuprizone-treated TG2(-/-) mice. In vitro TG2 overexpression in astrocytes coincided with more, while knock-down of TG2 with less fibronectin production. TG2 contributes, at least partly, to fibronectin production, and may play a role in fibronectin deposition during cuprizone-induced demyelination. Our observations are of interest in understanding the functional implications of TG2 during astrogliosis.
|Number of pages||13|
|Publication status||Published - 27-Jan-2017|
- MULTIPLE-SCLEROSIS LESIONS, CENTRAL-NERVOUS-SYSTEM, BLOOD-BRAIN-BARRIER, EXTRACELLULAR-MATRIX, GLIAL SCAR, CELL-ADHESION, CROSS-LINKING, GROWTH-FACTOR, AXONAL LOSS, REMYELINATION