Molecular and Cellular Biochemistry

, Volume 244, Issue 1–2, pp 69–76

Restricted neuronal expression of ubiquitous mitochondrial creatine kinase: Changing patterns in development and with increased activity

  • J. Boero
  • W. Qin
  • J. Cheng
  • T.A. Woolsey
  • A.W. Strauss
  • Z. Khuchua
Article

DOI: 10.1023/A:1022409101641

Cite this article as:
Boero, J., Qin, W., Cheng, J. et al. Mol Cell Biochem (2003) 244: 69. doi:10.1023/A:1022409101641

Abstract

Whereas ATP consumption increases with neural activity and is buffered by phosphocreatine (PCr), it is not known whether PCr synthesis by ubiquitous mitochondrial creatine kinase (uMtCK) supports energy metabolism in all neurons. To explore the possibility that uMtCK expression in neurons is modulated by activity and during development, we used immunocytochemistry to detect uMtCK-containing mitochondria. In the adult brain, subsets of neurons including layer Va pyramidal cells, most thalamic nuclei, cerebellar Purkinje cells, olfactory mitral cells and hippocampal interneurons strongly express uMtCK. uMtCK is transiently expressed by a larger group of neurons at birth. Neurons in all cortical layers express uMtCK at birth (P0), but uMtCK is restricted to layer Va by P12. uMtCK is detected in cerebellar Purkinje cells at birth, but localization to dendrites is only observed after P5 and is maximal on P14. Hippocampal CA1 and CA3 pyramidal neurons contain uMtCK-positive mitochondria at birth, but this pattern becomes progressively restricted to interneurons. Seizures induced uMtCK expression in cortical layers II–III and CA1 pyramidal neurons. In the cortex, but not in CA1, blockade of seizures prevented the induction of uMtCK. These findings support the concept that uMtCK expression in neurons is (1) developmentally regulated in post-natal life, (2) constitutively restricted in the adult brain, and (3) regulated by activity in the cortex and hippocampus. This implies that mitochondrial synthesis of PCr is restricted to those neurons that express uMtCK and may contribute to protect these cells during periods of increased energy demands.

brain cerebellum cortex creatine kinase hippocampus interneuron mitochondria olfactory seizures somatosensory 

Copyright information

© Kluwer Academic Publishers 2003

Authors and Affiliations

  • J. Boero
    • 1
  • W. Qin
    • 1
  • J. Cheng
    • 1
  • T.A. Woolsey
    • 2
  • A.W. Strauss
    • 3
  • Z. Khuchua
    • 3
  1. 1.Department of PediatricsWashington University School of MedicineSt. LouisUSA
  2. 2.Department of Neurology and Neurological SurgeryWashington University School of MedicineSt. LouisUSA
  3. 3.Department of PediatricsVanderbilt University Medical CenterNashvilleUSA

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