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L-Serine-Mediated Neuroprotection Includes the Upregulation of the ER Stress Chaperone Protein Disulfide Isomerase (PDI).
Dunlop, R A; Powell, J T; Metcalf, J S; Guillemin, G J; Cox, P A.
Afiliación
  • Dunlop RA; Brain Chemistry Labs, Institute for Ethnomedicine, Jackson Hole, WY, USA.
  • Powell JT; Neuroinflammation Group, MND and Neurodegenerative Diseases Research Center, Macquarie University, Sydney, Australia.
  • Metcalf JS; Brain Chemistry Labs, Institute for Ethnomedicine, Jackson Hole, WY, USA.
  • Guillemin GJ; Brain Chemistry Labs, Institute for Ethnomedicine, Jackson Hole, WY, USA.
  • Cox PA; Neuroinflammation Group, MND and Neurodegenerative Diseases Research Center, Macquarie University, Sydney, Australia.
Neurotox Res ; 33(1): 113-122, 2018 Jan.
Article en En | MEDLINE | ID: mdl-28975502
The unfolded protein response (UPR) is a highly evolutionarily conserved response to endoplasmic reticulum (ER) stress, which functions to return cells to homeostasis or send them into apoptosis, depending on the degree of cellular damage. ß-N-methylamino-L-alanine (L-BMAA) has been shown to induce ER stress in a variety of models and has been linked to several types of neurodegenerative disease including Guamanian amyotrophic lateral sclerosis/Parkinsonism dementia complex (ALS/PDC). L-Serine, an amino acid critical for cellular metabolism and neurological signaling, has been shown to be protective against L-BMAA-induced neurotoxicity in both animal and cell culture models. While the mechanisms of L-BMAA neurotoxicity have been well characterized, less is known about L-serine neuroprotection. We recently reported that L-serine and L-BMAA generate similar differential expression profiles in a human ER stress/UPR array, despite L-serine being neuroprotective and L-BMAA being linked to neurodegenerative disease. Here, we further investigate the mechanism(s) of L-serine-induced UPR dysregulation by examining key genes and proteins in the ER stress/UPR pathways. We report that L-serine selectively increased protein disulfide isomerase (PDI) protein translation, an ER chaperone involved in refolding misfolded proteins, suggesting it may be modulating the UPR to favor recovery from ER stress. This constitutes a new mechanism for L-serine-mediated neuroprotection and has implications for its use as a therapy for neurodegenerative illnesses.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Serina / Regulación hacia Arriba / Proteína Disulfuro Isomerasas / Estrés del Retículo Endoplásmico / Neuroprotección Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Neurotox Res Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Serina / Regulación hacia Arriba / Proteína Disulfuro Isomerasas / Estrés del Retículo Endoplásmico / Neuroprotección Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Neurotox Res Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos