Translocator protein (TSPO 18kDa) is expressed by neural stem and neuronal precursor cells
Abstract
Translocator protein 18 kDa, the peripheral benzodiazepine receptor by its earlier name, is a mitochondrial membrane protein associated with the mitochondrial permeability pore. While the function of the protein is not properly understood, it is known to play roles in necrotic and apoptotic processes of the neural tissue. In the healthy adult brain, TSPO expression is restricted to glial cells. In developing or damaged neural regions, however, TSPO appears in differentiating/regenerating neurons. Using immunocytochemical, molecular biological and cell biological techniques, we demonstrate that TSPO mRNA and protein, while missing from mature neurons, are present in neural stem cells and also in postmitotic neuronal precursors. Investigating some distinct stages of in vitro differentiation of NE-4C neural stem cells, TSPO 18 kDa was found to be repressed in a relatively late phase of neuron formation, when mature neuron-specific features appear. This timing indicates that mitochondria in fully developed neurons display specific characteristics and provides an additional marker for characterising neuronal differentiation.
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TSPO is present in immature neurons.
“Studies have demonstrated the presence of TSPO in immature neurons, as well as in differentiating/regenerating neurons [23, 24, 52].”
From Pharmacological modulation of TSPO in microglia/macrophages and neurons in a chronic neurodegenerative model of prion disease (2023) · cites this paper as [52]
TSPO is present in differentiating/regenerating neurons.
“Studies have demonstrated the presence of TSPO in immature neurons, as well as in differentiating/regenerating neurons [23, 24, 52].”
From Pharmacological modulation of TSPO in microglia/macrophages and neurons in a chronic neurodegenerative model of prion disease (2023) · cites this paper as [52]
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Lacapère, J.-J., & Papadopoulos, V. (2003) · Steroids · doi:10.1016/s0039-128x(03)00101-6 · Cited by 342 · see citing works
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Neuronal activity increases translocator protein (TSPO) levels
Notter, T., Schalbetter, S. M., Clifton, N. E., Mattei, D., Richetto, J., Thomas, K., Meyer, U., & Hall, J. (2021) · Molecular Psychiatry · doi:10.1038/s41380-020-0745-1 · Cited by 118 · see citing works
Vicente-Rodríguez, M., Mancuso, R., Peris-Yague, A., Simmons, C., NIMA Consortium, Wlazly, D., Dickinson, A., Foster, A., Knight, C., Leckey, C., et al. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02769-y · Cited by 17 · see citing works
“Studies have demonstrated the presence of TSPO in immature neurons, as well as in differentiating/regenerating neurons [23, 24, 52].”
Background
- Authors
- Varga, B., Markó, K., Hádinger, N., Jelitai, M., Demeter, K., Tihanyi, K., Vas, Á., & Madarász, E.
- Affiliations
- HUN-REN Institute of Experimental Medicine (HU)
- Gedeon Richter (Hungary) (HU)
- Venue
- Neuroscience Letters
- Publisher
- Elsevier BV
- Published
- 2009-09
- Volume
- 462
- Issue
- 3
- Pages
- 257-262
- ISSN
- 0304-3940 (ISSN-L)
- OpenAlex
- W2064193443
- Cited by
- 52
- References
- 1
- Citations by year
- 2025: 3 · 2024: 5 · 2023: 4 · 2022: 1 · 2021: 6 · 2020: 7 · 2019: 2 · 2018: 3 · 2017: 5 · 2016: 4 · 2015: 6 · 2014: 1 · 2013: 2 · 2012: 1
- FWCI
- 0.31
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience Letters (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Gedeon Richter
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pharmacological Receptor Mechanisms and Effects
- Keywords
- translocator protein (TSPO), neural stem cells, neuronal precursors, neuronal differentiation, mitochondrial proteins, apoptosis, necrosis
- MeSH terms
- Animals, Animals, Newborn, Brain, Cell Differentiation, Cells, Cultured, Embryo, Mammalian, Neurons, RNA, Messenger, Stem Cells, Receptors, GABA, Mice, Neural Plate
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