Your browser doesn't support javascript.
loading
Distinct proteomic profiles in prefrontal subareas of elderly major depressive disorder and bipolar disorder patients.
Qi, Yang-Jian; Lu, Yun-Rong; Shi, Li-Gen; Demmers, Jeroen A A; Bezstarosti, Karel; Rijkers, Erikjan; Balesar, Rawien; Swaab, Dick; Bao, Ai-Min.
Afiliación
  • Qi YJ; NHC and CAMS key laboratory of Medical Neurobiology, School of Brain Science and Brain Medicine, Department of Neurology of the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, PR China.
  • Lu YR; Department of Psychiatry, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Shi LG; Department of Neurosurgery, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Demmers JAA; Proteomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Bezstarosti K; Proteomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Rijkers E; Proteomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Balesar R; Netherlands Institute for Neuroscience, an Institute of the Royal Netherlands Academy of Arts and Sciences, Meibergdreef 47, 1105, BA, Amsterdam, The Netherlands.
  • Swaab D; NHC and CAMS key laboratory of Medical Neurobiology, School of Brain Science and Brain Medicine, Department of Neurology of the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, PR China. d.swaab@nin.knaw.nl.
  • Bao AM; Netherlands Institute for Neuroscience, an Institute of the Royal Netherlands Academy of Arts and Sciences, Meibergdreef 47, 1105, BA, Amsterdam, The Netherlands. d.swaab@nin.knaw.nl.
Transl Psychiatry ; 12(1): 275, 2022 07 11.
Article en En | MEDLINE | ID: mdl-35821008
ABSTRACT
We investigated for the first time the proteomic profiles both in the dorsolateral prefrontal cortex (DLPFC) and anterior cingulate cortex (ACC) of major depressive disorder (MDD) and bipolar disorder (BD) patients. Cryostat sections of DLPFC and ACC of MDD and BD patients with their respective well-matched controls were used for study. Proteins were quantified by tandem mass tag and high-performance liquid chromatography-mass spectrometry system. Gene Ontology terms and functional cluster alteration were analyzed through bioinformatic analysis. Over 3000 proteins were accurately quantified, with more than 100 protein expressions identified as significantly changed in these two brain areas of MDD and BD patients as compared to their respective controls. These include OGDH, SDHA and COX5B in the DLPFC in MDD patients; PFN1, HSP90AA1 and PDCD6IP in the ACC of MDD patients; DBN1, DBNL and MYH9 in the DLPFC in BD patients. Impressively, depending on brain area and distinct diseases, the most notable change we found in the DLPFC of MDD was 'suppressed energy metabolism'; in the ACC of MDD it was 'suppressed tissue remodeling and suppressed immune response'; and in the DLPFC of BD it was differentiated 'suppressed tissue remodeling and suppressed neuronal projection'. In summary, there are distinct proteomic changes in different brain areas of the same mood disorder, and in the same brain area between MDD and BD patients, which strengthens the distinct pathogeneses and thus treatment targets.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno Bipolar / Trastorno Depresivo Mayor Límite: Aged / Humans Idioma: En Revista: Transl Psychiatry Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno Bipolar / Trastorno Depresivo Mayor Límite: Aged / Humans Idioma: En Revista: Transl Psychiatry Año: 2022 Tipo del documento: Article