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1.
Nat Neurosci ; 22(10): 1731-1742, 2019 10.
Artículo en Inglés | MEDLINE | ID: mdl-31501572

RESUMEN

Mitochondria vary in morphology and function in different tissues; however, little is known about their molecular diversity among cell types. Here we engineered MitoTag mice, which express a Cre recombinase-dependent green fluorescent protein targeted to the outer mitochondrial membrane, and developed an isolation approach to profile tagged mitochondria from defined cell types. We determined the mitochondrial proteome of the three major cerebellar cell types (Purkinje cells, granule cells and astrocytes) and identified hundreds of mitochondrial proteins that are differentially regulated. Thus, we provide markers of cell-type-specific mitochondria for the healthy and diseased mouse and human central nervous systems, including in amyotrophic lateral sclerosis and Alzheimer's disease. Based on proteomic predictions, we demonstrate that astrocytic mitochondria metabolize long-chain fatty acids more efficiently than neuronal mitochondria. We also characterize cell-type differences in mitochondrial calcium buffering via the mitochondrial calcium uniporter (Mcu) and identify regulator of microtubule dynamics protein 3 (Rmdn3) as a determinant of endoplasmic reticulum-mitochondria proximity in Purkinje cells. Our approach enables exploring mitochondrial diversity in many in vivo contexts.


Asunto(s)
Encéfalo/citología , Mitocondrias/metabolismo , Neuronas/metabolismo , Enfermedad de Alzheimer/metabolismo , Enfermedad de Alzheimer/patología , Esclerosis Amiotrófica Lateral/metabolismo , Esclerosis Amiotrófica Lateral/patología , Animales , Astrocitos/metabolismo , Señalización del Calcio/genética , Señalización del Calcio/fisiología , Células Cultivadas , Cerebelo/citología , Ácidos Grasos/metabolismo , Humanos , Ratones , Ratones Transgénicos , Membranas Mitocondriales/metabolismo , Proteómica , Células de Purkinje/metabolismo
2.
Nat Commun ; 10(1): 3223, 2019 07 19.
Artículo en Inglés | MEDLINE | ID: mdl-31324793

RESUMEN

It is widely assumed that inositol trisphosphate (IP3) and ryanodine (Ry) receptors share the same Ca2+ pool in central mammalian neurons. We now demonstrate that in hippocampal CA1 pyramidal neurons IP3- and Ry-receptors are associated with two functionally distinct intracellular Ca2+ stores, respectively. While the IP3-sensitive Ca2+ store refilling requires Orai2 channels, Ry-sensitive Ca2+ store refilling involves voltage-gated Ca2+ channels (VGCCs). Our findings have direct implications for the understanding of function and plasticity in these central mammalian neurons.


Asunto(s)
Calcio/metabolismo , Hipocampo/metabolismo , Proteína ORAI2/metabolismo , Células Piramidales/metabolismo , Animales , Canales de Calcio , Regulación de la Expresión Génica , Fosfatos de Inositol/metabolismo , Iones , Ratones , Ratones Noqueados , Modelos Animales , Proteína ORAI2/genética , Canal Liberador de Calcio Receptor de Rianodina/metabolismo
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