The lesion in a new neurologically mutant mouse, Stumbler, has been studied using a Golgi technique and electron microscopy. Heterozygote Stumbler mice have smaller cerebella than their normal littermates from the earliest age studied (9 days postnatal). Purkinje cells have small immature-looking dendritic trees and retain somatic spines for up to 14 days longer than in normal mice. The Purkinje cells in the mutant also exhibit dark-staining organelles in their cytoplasm, as shown by light microscopy. By electron microscopy these organelles have been identified as mitochondria. Profiles of mitochondria are more abundant in both the Purkinje cell somata and dendrites of Stumbler mice, when compared to the normal. Purkinje cells are reduced in number from the earliest age studied, although degenerating Purkinje cells are not seen before P21. At this age, some of the remaining Purkinje cells in Stumbler begin to look almost normal, both in gross morphology and internal structure. No obvious changes in morphology have been seen in the granule cells but the population is reduced in number from P10 onwards. Some granule cell degeneration has been found in the Stumbler cerebellum, but this also occurs in the normal mouse at the same time, and therefore this has not been considered abnormal. The lesion in the cerebellar cortex of this mutant mouse is discussed with respect to the lesions found in some other mutant mice with cerebellar defects.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/0165-3806(81)90110-3 | DOI Listing |
Mol Biol Cell
January 2025
Department of Cell Biology, Emory University, 615 Michael St, Atlanta, GA, USA, 30322.
Rare inherited diseases caused by mutations in the copper transporters (CTR1) or induce copper deficiency in the brain, causing seizures and neurodegeneration in infancy through poorly understood mechanisms. Here, we used multiple model systems to characterize the molecular mechanisms by which neuronal cells respond to copper deficiency. Targeted deletion of CTR1 in neuroblastoma cells produced copper deficiency that produced a metabolic shift favoring glycolysis over oxidative phosphorylation.
View Article and Find Full Text PDFSTAR Protoc
January 2025
Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA; Initiative for Columbia Ataxia and Tremor, Columbia University, New York, NY 10032, USA. Electronic address:
As Purkinje cells of the cerebellum have a very fast firing rate, techniques with high temporal resolution are required to capture cerebellar physiology. Here, we present a protocol to record physiological signals in humans using cerebellar electroencephalography (cEEG). We describe steps for electrode placement and recording.
View Article and Find Full Text PDFBackground: Christianson syndrome (CS) is an x-linked recessive neurodevelopmental and neurodegenerative condition characterized by severe intellectual disability, cerebellar degeneration, ataxia, and epilepsy. Mutations to the gene encoding NHE6 are responsible for CS, and we recently demonstrated that a mutation to the rat gene causes a similar phenotype in the spontaneous rat model, which exhibits cerebellar degeneration with motor dysfunction. In previous work, we used the PhP.
View Article and Find Full Text PDFJ Clin Med
January 2025
Department of Clinical Therapeutics, Alexandra General Hospital, School of Medicine, National and Kapodistrian University of Athens, 11528 Athens, Greece.
Paraneoplastic cerebellar degeneration (PCD) is an inflammatory autoimmune process caused by onconeural antibodies directed against cerebellar Purkinje cells. In most cases, prognosis is poor as disease progression leads to pancerebellar dysfunction and permanent neurological damage. Through this case report, we aim to highlight the clinical presentation, diagnostic process, and therapeutic implications associated with PCD secondary to SCLC.
View Article and Find Full Text PDFInt J Mol Sci
January 2025
Department of Neuroregeneration, Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Meibergdreef 47, 1105 BA Amsterdam, The Netherlands.
Semaphorin 3A (Sema3A) is an axon guidance molecule, which is also abundant in the adult central nervous system (CNS), particularly in perineuronal nets (PNNs). PNNs are extracellular matrix structures that restrict plasticity. The cellular sources of Sema3A in PNNs are unknown.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!