Literature DB >> 31165281

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

Antonia G Vitalo1, Iulian Ilieş2, Günther K H Zupanc3.   

Abstract

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-D28k when their somata have reached diameters of approximately 10 μm, and they continue expression after they have grown to a final size of about 50 μm. Calbindin-D28k 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-D28k 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.

Entities:  

Keywords:  Apoptosis; Apteronotus leptorhynchus; Calbindin-D28k; Electromotoneuron; Neuroprotection

Year:  2019        PMID: 31165281     DOI: 10.1007/s00359-019-01343-3

Source DB:  PubMed          Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol        ISSN: 0340-7594            Impact factor:   1.836


  28 in total

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Authors:  G D Pappas; S G Waxman; M V Bennett
Journal:  J Neurocytol       Date:  1975-08

2.  Calbindin-D28k is expressed in osteoblastic cells and suppresses their apoptosis by inhibiting caspase-3 activity.

Authors:  T Bellido; M Huening; M Raval-Pandya; S C Manolagas; S Christakos
Journal:  J Biol Chem       Date:  2000-08-25       Impact factor: 5.157

3.  Locally reduced levels of acidic FGF lead to decreased expression of 28-kda calbindin and contribute to the selective vulnerability of the neurons in the entorhinal cortex in Alzheimer's disease.

Authors:  V Thorns; F Licastro; E Masliah
Journal:  Neuropathology       Date:  2001-09       Impact factor: 1.906

4.  Executioner caspase-3, -6, and -7 perform distinct, non-redundant roles during the demolition phase of apoptosis.

Authors:  E A Slee; C Adrain; S J Martin
Journal:  J Biol Chem       Date:  2000-10-31       Impact factor: 5.157

5.  Loss of calbindin-D28k from aging human cholinergic basal forebrain: relation to neuronal loss.

Authors:  Changiz Geula; Jing Bu; Nicholas Nagykery; Leonard F M Scinto; Jennifer Chan; Jeffrey Joseph; Robert Parker; Chuang-Kuo Wu
Journal:  J Comp Neurol       Date:  2003-01-06       Impact factor: 3.215

6.  Upregulation of calbindin-D28k expression during regeneration in the adult fish cerebellum.

Authors:  Marianne M Zupanc; Günther K H Zupanc
Journal:  Brain Res       Date:  2006-05-18       Impact factor: 3.252

7.  Pretreatment with PTD-calbindin D 28k alleviates rat brain injury induced by ischemia and reperfusion.

Authors:  Yongfeng Fan; Langfeng Shi; Yuehua Gu; Yanxin Zhao; Jun Xie; Jian Qiao; Guo-Yuan Yang; Yang Wang; Chuan-Zhen Lu
Journal:  J Cereb Blood Flow Metab       Date:  2006-07-26       Impact factor: 6.200

8.  Calbindin d28k overexpression protects striatal neurons from transient focal cerebral ischemia.

Authors:  M A Yenari; M Minami; G H Sun; T J Meier; D M Kunis; J R McLaughlin; D Y Ho; R M Sapolsky; G K Steinberg
Journal:  Stroke       Date:  2001-04       Impact factor: 7.914

9.  Age-related changes in calbindin-D28k, calretinin, and parvalbumin-immunoreactive neurons in the human cerebral cortex.

Authors:  Jing Bu; Vikram Sathyendra; Nicholas Nagykery; Changiz Geula
Journal:  Exp Neurol       Date:  2003-07       Impact factor: 5.330

10.  Calbindin-D28K-containing neurons in animal models of neurodegeneration: possible protection from excitotoxicity.

Authors:  A Iacopino; S Christakos; D German; P K Sonsalla; C A Altar
Journal:  Brain Res Mol Brain Res       Date:  1992-04
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