Differential loss of synaptic proteins in Alzheimer's disease: Implications for synaptic dysfunction

Article type: Research Article

Authors: Reddy, P. Hemachandra^{a; *} | Mani, Geethalakshmi^a | Park, Byung S.^b | Jacques, Joline^a | Murdoch, Geoffrey^c | Whetsell Jr., William^d | Kaye, Jeffrey^e | Manczak, Maria^a

Affiliations: [a] Neurogenetics Laboratory, Neurological Sciences Institute, Oregon Health & Science University, 505 N.W. 185th Avenue, Beaverton, OR 97006, USA | [b] Biostatistics and Bioinformatics Core, Oregon Health & Science University, 3181 S.W. Sam Jackson Park Rd, Portland, Oregon 97201, USA | [c] Department of Pathology, Oregon Health & Science University, 3181 S.W. Sam Jackson Park Rd, Portland, OR 97201, USA | [d] Department of Pathology, Vanderbilt University Medical Center, Nashville, TN 37232, USA | [e] Department of Neurology, Oregon Health & Science University, 3181 S.W. Sam Jackson Park Rd, Portland, OR 97201, USA

Correspondence: [*] Correspondind author: P. Hemachandra Reddy, Ph.D., Neurogenetics Laboratory, Neurological Sciences Institute, Oregon Health & Science University, 505 N.W. 185th Avenue, Beaverton, OR 97006, USA. Tel.: +1 503 418 2625; Fax: +1 503 418 2501; E-mail: [email protected].

Abstract: The objective of our research was to determine synaptic protein levels in brain specimens from AD subjects and age-matched control subjects. Further, to determine whether presynaptic or postsynaptic compartments of neurons are preferentially affected in AD patients, we studied 3 presynaptic vesicle proteins (synaptotagmin, synaptophysin, and Rab 3A), 2 synaptic membrane proteins (Gap 43 and synaptobrevin), and 2 postsynaptic proteins (neurogranin and synaptopodin) in specimens from AD and age-matched control brains. Two brain regions – the frontal and parietal cortices – were assessed for protein levels by immunoblotting analysis. We found a loss of both presynaptic vesicle proteins and postsynaptic proteins in all brain specimens from AD patients compared to those from age-matched control subjects. Further, we found that the loss of synaptic proteins was more severe in the frontal cortex brain specimens than in the parietal cortex brain specimens from the AD subjects compared to those from the control subjects, suggesting that the frontal brain may be critical for synaptic function in AD. Using immunohistochemistry techniques, we also determined the distribution pattern of all synaptic proteins in both the frontal and parietal cortices brain specimens from control subjects. Of the 7 synaptic proteins studied, the presynaptic proteins synaptophysin and rab 3A and the postsynaptic protein synaptopodin were the most down-regulated. Our study suggests that postsynaptic proteins and presynaptic proteins are important for synaptic function and may be related to cognitive impairments in AD.

Keywords: synaptopodin, synaptophysin, Alzheimer's disease, synaptic protein, cognitive decline

DOI: 10.3233/JAD-2005-7203

Journal: Journal of Alzheimer's Disease, vol. 7, no. 2, pp. 103-117, 2005