4.6 Review

Tenascins in CNS lesions

Journal

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
Volume 89, Issue -, Pages 118-124

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2018.09.012

Keywords

Central nervous system; Extracellular matrix; Lesion; Neuroinflammation; Synaptic plasticity; Regeneration; Stem cell niche; Tenascin

Funding

  1. Stem Cell Network North Rhine Westphalia
  2. German Research Foundation (Deutsche Forschungsgemeinschaft, DFG) [SFB 509, SFB 642, SPP-1109, SPP-1172, Fa 159/11-1, Fa 159/16-1, GRK 736, GSC 98/1, SPP-1757, Fa 159/20-1,2, Fa 159/22-1]
  3. German Ministry of Education, Research and Technology (Bundesministerium fur Bildung und Forschung) [BMBF 01GN0503]
  4. Ruhr-University (International Graduate School of Neuroscience and President's special programme call 2008)

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The tenascin family of glycoproteins comprises four members in vertebrates, of which tenascin-C (Tnc) and tenascin-R (Tnr) are particularly important in the context of lesions in the central nervous system (CNS). Tnc is expressed in the developing CNS, before it is down-regulated and mainly restricted to the adult neural stem cell niches. It regulates numerous processes including differentiation, adhesion, migration and neurite outgrowth. These aspects are critical in the developing organism, but also after damage. Interestingly, Tnc is indeed re expressed in the injured CNS. Additionally, Tnc is an activator of the immune response, another important aspect after lesion. Tnr is part of perineuronal nets, a specialized form of extracellular matrix that enwraps subtypes of neurons and limits synaptic plasticity. We summarize the role of tenascins in the context of stem cell niches, barrier formation, synaptic plasticity and immune response in the damaged mammalian CNS.

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