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Microglial cell activation and senescence are characteristic of the pathology FXTAS.
Martínez Cerdeño, Verónica; Hong, Tiffany; Amina, Sarwat; Lechpammer, Mirna; Ariza, Jeanelle; Tassone, Flora; Noctor, Stephen C; Hagerman, Paul; Hagerman, Randi.
Afiliación
  • Martínez Cerdeño V; Department of Pathology and Laboratory Medicine, UC Davis School of Medicine, Sacramento, California, USA.
  • Hong T; Institute for Pediatric Regenerative Medicine and Shriners Hospitals for Children of Northern California, Sacramento, California, USA.
  • Amina S; MIND Institute, UC Davis Medical Center, Sacramento, California, USA.
  • Lechpammer M; Department of Pathology and Laboratory Medicine, UC Davis School of Medicine, Sacramento, California, USA.
  • Ariza J; Institute for Pediatric Regenerative Medicine and Shriners Hospitals for Children of Northern California, Sacramento, California, USA.
  • Tassone F; Institute for Pediatric Regenerative Medicine and Shriners Hospitals for Children of Northern California, Sacramento, California, USA.
  • Noctor SC; MIND Institute, UC Davis Medical Center, Sacramento, California, USA.
  • Hagerman P; Department of Pathology and Laboratory Medicine, UC Davis School of Medicine, Sacramento, California, USA.
  • Hagerman R; Department of Pathology and Laboratory Medicine, UC Davis School of Medicine, Sacramento, California, USA.
Mov Disord ; 33(12): 1887-1894, 2018 12.
Article en En | MEDLINE | ID: mdl-30537011
BACKGROUND: Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder associated with premutation alleles of the FMR1 gene. Expansions of more than 200 CGG repeats give rise to fragile X syndrome, the most common inherited form of cognitive impairment. Fragile X-associated tremor/ataxia syndrome is characterized by cerebellar tremor and ataxia, and the presence of ubiquitin-positive inclusions in neurons and astrocytes. It has been previously suggested that fragile X-associated tremor/ataxia syndrome is associated with an inflammatory state based on signs of oxidative stress-mediated damage and iron deposition. OBJECTIVE: Determine whether the pathology of fragile X-associated tremor/ataxia syndrome involves microglial activation and an inflammatory state. METHODS: Using ionized calcium binding adaptor molecule 1 and cluster differentiation 68 antibodies to label microglia, we examined the number and state of activation of microglial cells in the putamen of 13 fragile X-associated tremor/ataxia syndrome and 9 control postmortem cases. RESULTS: Nearly half of fragile X-associated tremor/ataxia syndrome cases (6 of 13) presented with dystrophic senescent microglial cells. In the remaining fragile X-associated tremor/ataxia syndrome cases (7 of 13), the number of microglial cells and their activation state were increased compared to controls. CONCLUSIONS: The presence of senescent microglial cells in half of fragile X-associated tremor/ataxia syndrome cases suggests that this indicator could be used, together with the presence of intranuclear inclusions and the presence of iron deposits, as a biomarker to aid in the postmortem diagnosis of fragile X-associated tremor/ataxia syndrome. An increased number and activation indicate that microglial cells play a role in the inflammatory state present in the fragile X-associated tremor/ataxia syndrome brain. Anti-inflammatory treatment of patients with fragile X-associated tremor/ataxia syndrome may be indicated to slow neurodegeneration. © 2018 International Parkinson and Movement Disorder Society.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ataxia / Temblor / Encéfalo / Astrocitos / Enfermedades Neurodegenerativas / Síndrome del Cromosoma X Frágil Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ataxia / Temblor / Encéfalo / Astrocitos / Enfermedades Neurodegenerativas / Síndrome del Cromosoma X Frágil Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos