Microperoxisomes in the central nervous system of the postnatal rat
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Peroxisome and pexophagy in neurological diseases
2024, Fundamental ResearchImpaired neurogenesis and associated gliosis in mouse brain with PEX13 deficiency
2018, Molecular and Cellular NeuroscienceCitation Excerpt :These abnormalities are believed to reflect the importance of peroxisomes in brain development (Faust et al., 2005; Baes et al., 1997). In support of this premise, peroxisome abundance is high at neurite terminals of differentiating neurons during development, suggesting a role in neurite growth and synapse formation (McKenna et al., 1976; Arnold and Holtzman, 1978). Peroxisomes play a role in the synthesis of plasmalogens, and therefore contribute to membrane stability and second messenger function, as well as being a major component of myelin sheaths (Brites et al., 2004), and docosahexaenoic acid (DHA), which has a significant role in neurotransmission, fine synaptic remodeling, and calcium homeostasis (Salem et al., 2001; Chapkin et al., 2009).
Peroxisomes in brain development and function
2016, Biochimica et Biophysica Acta - Molecular Cell ResearchCitation Excerpt :Moreover, the abundance of brain peroxisomes differs between brain areas. Although single membrane-bound structures – detectable with different methods to stain peroxisomes – can be found in most regions, some brain areas were reported to contain only modest numbers of peroxisomes [22]. However, peroxisome abundance also changes during development.
Be different-The diversity of peroxisomes in the animal kingdom
2010, Biochimica et Biophysica Acta - Molecular Cell ResearchCitation Excerpt :Besides brain, the peroxisomal enzymes involved in ether lipid synthesis predominate in tissues known to synthesize wax esters and ether lipids (e. g. sebaceous glands such as uropygial glands of birds, preputial, meibomian or perianal glands). Generally, peroxisomes are found in developing neurons in higher concentrations than in differentiated ones and are enriched at axon and dendrite terminals, a localization that is not prominent in adult neurons [222]. With respect to their distribution among different brain regions, immunostaining against catalase as standard marker enzyme was used for localization [223,224].
Peroxisomal multifunctional protein-2 deficiency causes motor deficits and glial lesions in the adult central nervous system
2006, American Journal of Pathology