A novel cytosolic phosphoprotein, DP58 induced in bone marrow-derived dendritic progenitors was found in this study to be constitutively expressed at a very high level in neuronal nuclei. Amplified cDNA confirmed by sequencing to be DP58 was present only in brain tissue, and DP58-like protein was expressed in neurons as a 52 kDa nuclear protein, phosphorylated primarily at the serine residues. In contrast, its isoform in dendritic progenitors appeared as a 58 kDa inducible protein with phosphorylation at serine, threonine and tyrosine residues. Although protein markers common to brain and hematopoietic cells are known, no report was found on constitutive expression in neuronal nuclei of DP58, an inducible Pro-myloid marker. The sequence of DP58 reveals ankyrin repeats present in a wide spectrum of interacting proteins including NF-kappaB-binding BCL3, a predominantly nuclear protein of I-kappaB family. The contrasting phosphorylated forms of DP58 suggest a distinct physiological role in neuronal cells and early dendritic progenitors.
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http://dx.doi.org/10.2741/2284 | DOI Listing |
Pharmaceuticals (Basel)
December 2024
Department of Medical Biosciences, University of the Western Cape, Bellville 7535, South Africa.
Adverse complications like metabolic disorders, neurotoxicity, and low central nervous system (CNS) penetration are associated with the long-term use of tenofovir disoproxil fumarate (TDF). Therefore, some modifications are required to enhance neurological functions using silver nanoparticles (AgNPs). This study aimed to evaluate the neuroprotective impact of silver nanoparticles (AgNPs)-conjugated TDF as AgNPs-TDF on the hippocampal microanatomy and some neuro-biomarkers of diabetic rats.
View Article and Find Full Text PDFJ Neuroendocrinol
January 2025
Department of Psychology, Columbia University, New York, New York, USA.
Among contributors to diffusible signaling are portal systems which join two capillary beds through connecting veins. Portal systems allow diffusible signals to be transported in high concentrations directly from one capillary bed to the other without dilution in the systemic circulation. Two portal systems have been identified in the brain.
View Article and Find Full Text PDFParkinsons disease (PD) is considered one of the most frequent neurological diseases in the world. There is a need to study the early and efficient biomarkers of Parkinsons, such as changes in structural disorders like DNA and chromatin, especially at the subcellular level in the human brain. We used two techniques, Partial wave spectroscopy (PWS) and Inverse Participation Ratio (IPR), to detect the changes in structural disorder in the human brain tissue samples.
View Article and Find Full Text PDFStructural changes involving new neurons can occur through stem cell-driven neurogenesis and late-maturing immature neurons, namely undifferentiated neuronal precursors frozen in a state of arrested maturation. The latter exist in the cerebral cortex, being particularly abundant in large-brained mammals. Similar cells have been described in the amygdala of some species, although their interspecies variation remain poorly understood.
View Article and Find Full Text PDFIt is becoming more broadly accepted that human-based models are needed to better understand the complexities of the human nervous system and its diseases. The recently developed human brain organotypic culture model is one highly promising model that requires the involvement of neurosurgeons and neurosurgical patients. Studies have investigated the electrophysiological properties of neurons in such human tissues, but the maintenance of other cell types within explanted brain remains largely unknown.
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