SPID#: 47 In order to determine whether there are age-related changes in the supragranular layer of the dentate gyrus of the rhesus monkey, we examined this layer in monkeys 4 to 35 years of age, spanning the entire range of adulthood of this species. Electron microscopic analyses of this region were conducted to determine whether there is an age-related change in the number of synapsing axon terminals, in the cross-sectional area of these terminals, or in the length of the postsynaptic density at the synaptic junction. In a subset of our monkeys (n = 6, ages 4 to 31 years), we compared three different approaches to the estimation of synaptic density (1) the conventional method, in which synapse numbers are expressed per unit area of the examined tissue section; (2) the empirical formula of Colonnier and Beaulieu for converting areal densities into number of synapses per unit volume; and (3) the disector method, a stereological approach to the estimation of number of synapses per unit volume that makes no assumption about the shape of the objects. The three methods were highly intercorrelated (r's = .89), and none of the methods revealed an age-related loss of synapses. In addition, the conventional method showed no age-related change in the number of axodendritic or axospinous synapses, the size of cross-sectional area of the synapsing terminals, or the length of the postsynaptic densities of synapses. Thus, since the synapses in the supragranular layer of the dentate gyrus do not change, one has to look somewhere else for structural changes that could be considered responsible for age-related cognitive decline and memory loss. Tissues of all monkeys were shared with other projects.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
2P51RR000165-36
Application #
5219902
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
36
Fiscal Year
1996
Total Cost
Indirect Cost
Fonseca, Jairo A; McCaffery, Jessica N; Caceres, Juan et al. (2018) Inclusion of the murine IgG? signal peptide increases the cellular immunogenicity of a simian adenoviral vectored Plasmodium vivax multistage vaccine. Vaccine 36:2799-2808
Tedesco, Dana; Thapa, Manoj; Chin, Chui Yoke et al. (2018) Alterations in Intestinal Microbiota Lead to Production of Interleukin 17 by Intrahepatic ?? T-Cell Receptor-Positive Cells and Pathogenesis of Cholestatic Liver Disease. Gastroenterology 154:2178-2193
Robinson, Amy A; Abraham, Carmela R; Rosene, Douglas L (2018) Candidate molecular pathways of white matter vulnerability in the brain of normal aging rhesus monkeys. Geroscience 40:31-47
Walker, Lary C (2018) Sabotage by the brain's supporting cells helps fuel neurodegeneration. Nature 557:499-500
Mascaro, Jennifer S; Rentscher, Kelly E; Hackett, Patrick D et al. (2018) Preliminary evidence that androgen signaling is correlated with men's everyday language. Am J Hum Biol 30:e23136
Forger, Nancy G; Ruszkowski, Elara; Jacobs, Andrew et al. (2018) Effects of sex and prenatal androgen manipulations on Onuf's nucleus of rhesus macaques. Horm Behav 100:39-46
Claw, Katrina G; George, Renee D; MacCoss, Michael J et al. (2018) Quantitative evolutionary proteomics of seminal fluid from primates with different mating systems. BMC Genomics 19:488
Adekambi, Toidi; Ibegbu, Chris C; Cagle, Stephanie et al. (2018) High Frequencies of Caspase-3 Expressing Mycobacterium tuberculosis-Specific CD4+ T Cells Are Associated With Active Tuberculosis. Front Immunol 9:1481
Beck, Goichi; Maehara, Shunsuke; Chang, Phat Ly et al. (2018) A Selective Phosphodiesterase 10A Inhibitor Reduces L-Dopa-Induced Dyskinesias in Parkinsonian Monkeys. Mov Disord 33:805-814
Georgieva, Maria; Sia, Jonathan Kevin; Bizzell, Erica et al. (2018) Mycobacterium tuberculosis GroEL2 Modulates Dendritic Cell Responses. Infect Immun 86:

Showing the most recent 10 out of 912 publications