{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,30]],"date-time":"2025-08-30T16:50:56Z","timestamp":1756572656534,"version":"3.41.0"},"reference-count":32,"publisher":"Baishideng Publishing Group Inc.","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["World J Psychiatry"],"abstract":"<jats:p>BACKGROUND<\/jats:p>\n          <jats:p>Alzheimer\u2019s disease (AD) is a progressive neurodegenerative disorder currently lacking effective therapeutic interventions. Pathological hallmarks of AD include intracellular neurofibrillary tangles (NFTs) and extracellular amyloid beta (A\u03b2) plaques. Neuroplastin 65 (NP65), highly expressed in the brain, has been previously shown to mitigate cognitive impairments and decrease A\u03b2 plaques in the AD mouse model, suggesting that NP65 is involved in AD neuropathology. However, direct evidence linking NP65 expression to AD pathogenesis in human brain remains absent.<\/jats:p>\n          <jats:p>AIM<\/jats:p>\n          <jats:p>To quantify NP65 isoform expression gradients across distinct neuroanatomical regions in the healthy brain and investigate the alterations of NP65 expression in the AD brain.<\/jats:p>\n          <jats:p>METHODS<\/jats:p>\n          <jats:p>Immunohistochemical, immunofluorescent and western blot analyses were used to investigate NP65 expression in 19 postmortem brains (AD = 10, controls = 9). Double immunostaining with 6E10 and or phosphorylated-microtubule-associated protein tau (AT-8, a marker for NFT) markers was performed to assess NP65 colocalization with A\u03b2 plaques and NFTs.<\/jats:p>\n          <jats:p>RESULTS<\/jats:p>\n          <jats:p>In controls, NP65 was highly expressed in a wide-range of brain areas. AD cases showed significantly increased NP65 immunoreactivity across multiple brain regions, including the frontal and temporal cortex, hippocampus, and cerebellum, compared to controls. Western blot analysis consistently confirmed significantly elevated NP65 expression in the hippocampus of AD patients relative to controls. Double immunostaining demonstrated partial colocalization of NP65 with NFTs and A\u03b2 plaques in AD brain tissue.<\/jats:p>\n          <jats:p>CONCLUSION<\/jats:p>\n          <jats:p>Our findings demonstrate a significant increase of NP65 protein, which colocalizes with NFTs and A\u03b2 plaques in AD brains, providing direct evidence supporting a critical role of NP65 expression in the neuropathological mechanisms of this disease.<\/jats:p>","DOI":"10.5498\/wjp.v15.i6.105751","type":"journal-article","created":{"date-parts":[[2025,5,29]],"date-time":"2025-05-29T02:07:01Z","timestamp":1748484421000},"source":"Crossref","is-referenced-by-count":1,"title":["Increased expression of the neuroplastin 65 protein is involved in neurofibrillary tangles and amyloid beta plaques in Alzheimer\u2019s disease"],"prefix":"10.5498","volume":"15","author":[{"given":"Ya-Ni","family":"Zheng","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yan","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ling","family":"Chen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Li-Zhang","family":"Xu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lei","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jia-Lu","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Juan","family":"Liu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Qi-Lei","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Qiong-Lan","family":"Yuan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"2060","published-online":{"date-parts":[[2025,6,19]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(20)32205-4"},{"key":"B2","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(15)01124-1"},{"key":"B3","doi-asserted-by":"publisher","DOI":"10.1097\/NEN.0b013e3181919a48"},{"key":"B4","doi-asserted-by":"publisher","DOI":"10.3390\/ijms241813900"},{"key":"B5","doi-asserted-by":"publisher","DOI":"10.1038\/s41573-022-00391-w"},{"key":"B6","doi-asserted-by":"publisher","DOI":"10.1016\/j.nbd.2013.04.014"},{"key":"B7","doi-asserted-by":"publisher","DOI":"10.3390\/biomedicines12081726"},{"key":"B8","doi-asserted-by":"publisher","DOI":"10.3389\/fncel.2023.1129773"},{"key":"B9","doi-asserted-by":"publisher","DOI":"10.1074\/jbc.272.2.821"},{"key":"B10","doi-asserted-by":"publisher","DOI":"10.1016\/j.brainres.2006.11.090"},{"key":"B11","doi-asserted-by":"publisher","DOI":"10.1016\/s0014-5793(98)00616-4"},{"key":"B12","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.080389297"},{"key":"B13","unstructured":"Kreutz MR, Langnaese K, Dieterich DC, Seidenbecher CI, Zuschratter W, Beesley PW, Gundelfinger ED. 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