4.3 Article

Calbindin-D28k expression in spinal electromotoneurons of the weakly electric fish Apteronotus leptorhynchus during adult development and regeneration

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SPRINGER HEIDELBERG
DOI: 10.1007/s00359-019-01343-3

关键词

Electromotoneuron; Calbindin-D-28k; Apoptosis; Neuroprotection; Apteronotus leptorhynchus

资金

  1. Northeastern University
  2. National Science Foundation [1538505]
  3. Div Of Civil, Mechanical, & Manufact Inn
  4. Directorate For Engineering [1538505] Funding Source: National Science Foundation

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Additive neurogenesis, the net increase in neuronal numbers by addition of new nerve cells to existing tissue, forms the basis for indeterminate spinal cord growth in brown ghost knifefish (Apteronotus leptorhynchus). Among the cells generated through the activity of adult neural stem cells are electromotoneurons, whose axons constitute the electric organ of this weakly electric fish. Electromotoneuron development is organized along a caudo-rostral gradient, with the youngest and smallest of these cells located near the caudal end of the spinal cord. Electromotoneurons start expressing calbindin-D-28k when their somata have reached diameters of approximately 10 mu m, and they continue expression after they have grown to a final size of about 50 mu m. Calbindin-D-28k expression is significantly increased in young neurons generated in response to injury. Immunohistochemical staining against caspase-3 revealed that electromotoneurons in both intact and regenerating spinal cord are significantly less likely to undergo apoptosis than the average spinal cord cell. We hypothesize that expression of calbindin-D-28k protects electromotoneurons from cell death; and that the evolutionary development of such a neuroprotective mechanism has been driven by the indispensability of electromotoneurons in the fish's electric behavior, and by the high size-dependent costs associated with their production or removal upon cell death.

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