The Morphology Core (A) is an integrated cellular, histological and pathological laboratory focusing on providing tissue processing and histological expertise, state of the art microscopy and image analyses, whole animal imaging technologies and skin specific pathological interpretation. The Morphology Core has expanded its focus and has added new areas of technology to reflect the shift in projects undertaken by SDRC faculty utilizing the Morphology Core. There has been a very high demand for sophisticated high throughput confocal imaging as well as live cell imaging capabilities, computer-assisted image analysis, preparation of tissue for laser capture microdissection and flow cytometry. As a consequence, the Morphology Core has maintained resources for high-demand services and committed resources to these new demand areas, as reflected in the Specific Aims.
Specific Aim I. Provide cost effective state-of-the-art skin specific histological, microscopic, morphometric and analytic imaging services and expertise to promote skin-related research including (i) embedding, sectioning, and staining facilities, routine histology services for human and murine samples;(ii) immunolocalization methods for morphological studies;(iii) expert microscopy and photo-microscopy with hands-on training in a range of microscopic technologies;(iv) expert pathology consultation of human and mouse tissue, (v) experimental design assistance for experiments requiring morphological analysis, including macro development, statistical planning and analysis;(vi) quantitative image analysis;(vii) confocal laser microscopy;(viii) laser capture microdissection;and (ix) flow cytometry. Included in this application are new resource(s) for SDRC members including (i) spinning disk confocal microscopy, including live cell imaging and high throughput screening technologies;(ii) small animal imaging and (iii) in house flow cytometry.
Specific Aim II. Provide expertise in morphologic techniques that facilitate a "pipeline" of translational research and interdisciplinary projects involving skin research. The Morphology Core promotes novel bidirectional research that benefits patients with skin disease by supporting projects that lead from bedside to bench and bench to bedside {translational research). Additional goals include disseminating technical information among SDRC members, encouraging resource sharing, providing mentorship, and enhancing collaborations that promote interdisciplinary exchange of ideas and expertise.

Public Health Relevance

The Morphology Core provides expert knowledge for skin-specific tissue analyses, protocol development and morphological and pathological analyses, and provides expertise and training in microscopy and image analyses and evolves and changes to meet the needs of new SDRC investigators and new research directions. The Morphology core is heavily utilized and is integral to the success of the SDRC.

National Institute of Health (NIH)
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Center Core Grants (P30)
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Special Emphasis Panel (ZAR1-HL)
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Case Western Reserve University
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Santilli, S; Kast, D R; Grozdev, I et al. (2016) Visualization of atherosclerosis as detected by coronary artery calcium and carotid intima-media thickness reveals significant atherosclerosis in a cross-sectional study of psoriasis patients in a tertiary care center. J Transl Med 14:217
Fritz, Yi; Klenotic, Philip A; Swindell, William R et al. (2016) Induction of Alternative Proinflammatory Cytokines Accounts for Sustained Psoriasiform Skin Inflammation in IL-17C+IL-6KO Mice. J Invest Dermatol :
Bhaskaran, N; Quigley, C; Weinberg, A et al. (2016) Transforming growth factor-β1 sustains the survival of Foxp3(+) regulatory cells during late phase of oropharyngeal candidiasis infection. Mucosal Immunol 9:1015-26
Hatter, Alyn D; Soler, David C; Curtis, Christine et al. (2016) Case report of individual with cutaneous immunodeficiency and novel 1p36 duplication. Appl Clin Genet 9:1-4
Hoarau, G; Mukherjee, P K; Gower-Rousseau, C et al. (2016) Bacteriome and Mycobiome Interactions Underscore Microbial Dysbiosis in Familial Crohn's Disease. MBio 7:
Monin, Leticia; Gudjonsson, Johann E; Childs, Erin E et al. (2016) MCPIP1/Regnase-1 Restricts IL-17A- and IL-17C-Dependent Skin Inflammation. J Immunol :
Das, Lopa M; Binko, Amy M; Traylor, Zachary P et al. (2016) Early indicators of survival following exposure to mustard gas: Protective role of 25(OH)D. Toxicol Lett 248:9-15
Wang, Yunmei; Golden, Jackelyn B; Fritz, Yi et al. (2016) Interleukin 6 regulates psoriasiform inflammation-associated thrombosis. JCI Insight 1:e89384
Zhang, Ling-Juan; Sen, George L; Ward, Nicole L et al. (2016) Antimicrobial Peptide LL37 and MAVS Signaling Drive Interferon-β Production by Epidermal Keratinocytes during Skin Injury. Immunity 45:119-30
Li, Yong; Stoll, Stefan W; Sekhon, Sahil et al. (2016) Transgenic expression of human amphiregulin in mouse skin: inflammatory epidermal hyperplasia and enlarged sebaceous glands. Exp Dermatol 25:187-93

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