? PATHOLOGY CORE The pathological assessment of old animals is important to determine whether the changes observed as animals age are associated with or independent of underlying pathological conditions. It is, therefore, essential to obtain accurate and thorough pathological assessments of aging animals. The Pathology Core will play a key role in the San Antonio Nathan Shock Aging Center because pathology increases exponentially with advancing age and is largely responsible for age-related morbidity and mortality. Knowledge of the pathological lesions associated with interventions used to study aging is essential to interpreting the impact of these interventions on the aging process(es). This knowledge will also provide insight into the underlying mechanism(s) behind the interventions' effects. The Pathology Core will build on the extensive experience of researchers at San Antonio and the expertise of the Core Leaders in pathological analyses of experimental animal models. Thus, the Specific Aims of the Pathology Core are: 1. To conduct comprehensive end-of-life and cross-sectional pathological analyses of established and new rodent models as well as other species used in aging research that die spontaneously or are sacrificed at specific age points in colonies maintained by the Aging Animal Models and Longevity Assessment Core. 2. To conduct immunohistochemical, molecular, and quantitative morphometric analyses of the tissues/organs of rodent models and other species by performing a) morphometric and immunohistochemical analyses on several lesions and age-related histological changes and b) in situ hybridization to further analyze the histological changes at the molecular level. 3. To continue to a) accrue a comprehensive database of histopathological data and images as a resource for analyses by investigators, b) provide basic pathological information for new investigations, and c) create a tissue archive by collecting and storing tissue samples (paraffin and frozen blocks) as a resource for analyses of samples as requested and for new morphological research. 4. To provide histopathology services for investigators by preparing paraffin and frozen blocks, making unstained slides, and performing various staining (including special staining). New services include (a) making tissue array slides for histological/morphological experiments, and (b) performing laser capture microdissection for further molecular analyses. 5. To assist faculty and students interested in the basic biology of animal models with the pathological analyses needed for grant applications and manuscript preparation.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
2P30AG013319-21
Application #
8959555
Study Section
Special Emphasis Panel (ZAG1-ZIJ-2 (M1))
Project Start
Project End
Budget Start
2015-07-15
Budget End
2016-06-30
Support Year
21
Fiscal Year
2015
Total Cost
$114,227
Indirect Cost
$39,078
Name
University of Texas Health Science Center
Department
Type
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Gelfond, Jonathan; Goros, Martin; Hernandez, Brian et al. (2018) A System for an Accountable Data Analysis Process in R. R J 10:6-21
Sills, Aubrey M; Artavia, Joselyn M; DeRosa, Brian D et al. (2018) Long-term treatment with the mTOR inhibitor rapamycin has minor effect on clinical laboratory markers in middle-aged marmosets. Am J Primatol :e22927
Xu, Ming; Pirtskhalava, Tamar; Farr, Joshua N et al. (2018) Senolytics improve physical function and increase lifespan in old age. Nat Med 24:1246-1256
Unnikrishnan, Archana; Hadad, Niran; Masser, Dustin R et al. (2018) Revisiting the genomic hypomethylation hypothesis of aging. Ann N Y Acad Sci 1418:69-79
Van Skike, Candice E; Jahrling, Jordan B; Olson, Angela B et al. (2018) Inhibition of mTOR protects the blood-brain barrier in models of Alzheimer's disease and vascular cognitive impairment. Am J Physiol Heart Circ Physiol 314:H693-H703
Mao, Kai; Quipildor, Gabriela Farias; Tabrizian, Tahmineh et al. (2018) Late-life targeting of the IGF-1 receptor improves healthspan and lifespan in female mice. Nat Commun 9:2394
Lee, Hak Joo; Feliers, Denis; Barnes, Jeffrey L et al. (2018) Hydrogen sulfide ameliorates aging-associated changes in the kidney. Geroscience 40:163-176
Kang, Donghoon; Kirienko, Daniel R; Webster, Phillip et al. (2018) Pyoverdine, a siderophore from Pseudomonas aeruginosa, translocates into C. elegans, removes iron, and activates a distinct host response. Virulence 9:804-817
Hook, Michael; Roy, Suheeta; Williams, Evan G et al. (2018) Genetic cartography of longevity in humans and mice: Current landscape and horizons. Biochim Biophys Acta Mol Basis Dis 1864:2718-2732
Van Skike, Candice E; Galvan, Veronica (2018) A Perfect sTORm: The Role of the Mammalian Target of Rapamycin (mTOR) in Cerebrovascular Dysfunction of Alzheimer's Disease: A Mini-Review. Gerontology 64:205-211

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