The Tissue Culture and Histology Core was established to facilitate skin-related research by providing a platform that allows access to state of the art experimental human and rodent skin model systems at the tissue and cellular level. For tissue analysis, the TCHC provides a wide array of histological;immunohistochemical;and molecular-based tools to characterize gross and microscopic morphology, functional features, and gene expression in skin of mutant and genetically engineered laboratory animals. The TCHC is also dedicated to assisting Center investigators in the isolation, propagation and manipulation of primary skin cells in two and three-dimensional culture systems and in analysis of genes related to skin diseases by efficient and systematic generation of transgenic tissue models of skin that show either transgene overexpression or suppression. The TCHC is equipped with special technical expertise that includes extensive knowledge of skin and hair follicle morphology essential for understanding the genotype/phenotype correlations;state of the art methods for gene expression studies specifically designed for mouse and human skin and cells;and possession of a battery of original experimental approaches to the study of skin physiology in vivo. The TCHC will also provide Center investigators with proofreading and suggestions for Materials &Methods sections for publications and applications for extramural research funding ufilizing skin and cellular analyses. Finally, the TCHC provides several new areas of innovation to Center investigators. Tissue microarrays of human normal and diseased skin will be generated for Center investigators upon request with the hopes of enriching the interactions between Dermatopathologists and CUMCSDRC basic scientists. In an effort to broaden the appeal of the TCHC within the Columbia research community, we have enhanced our repertoire of skin stem cell services including: in vitro and in vivo functional stem cell assays, induced pluripotent stem cell production from human skin cells, and microRNA profiling of adult skin stem cells. Overall, we feel the TCHC provides a comprehensive catalog of experimental technical expertise and knowledge of skin biology that will fully support the skin-related research of Center investigators, increase clinician-researcher interactions and reduce research costs.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
5P30AR044535-12
Application #
8499258
Study Section
Special Emphasis Panel (ZAR1-HL)
Project Start
Project End
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
12
Fiscal Year
2013
Total Cost
$297,663
Indirect Cost
$112,780
Name
Columbia University (N.Y.)
Department
Type
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
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Harris, John E; Rashighi, Mehdi; Nguyen, Nhan et al. (2016) Rapid skin repigmentation on oral ruxolitinib in a patient with coexistent vitiligo and alopecia areata (AA). J Am Acad Dermatol 74:370-1
Mathew, Grinu; Hannan, Abdul; Hertzler-Schaefer, Kristina et al. (2016) Targeting of Ras-mediated FGF signaling suppresses Pten-deficient skin tumor. Proc Natl Acad Sci U S A 113:13156-13161
Shen, Yao; Kim, Arianna L; Du, Rong et al. (2016) Transcriptome Analysis Identifies the Dysregulation of Ultraviolet Target Genes in Human Skin Cancers. PLoS One 11:e0163054
Dai, Zhenpeng; Xing, Luzhou; Cerise, Jane et al. (2016) CXCR3 Blockade Inhibits T Cell Migration into the Skin and Prevents Development of Alopecia Areata. J Immunol 197:1089-99
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Dainichi, Teruki; Hayden, Matthew S; Park, Sung-Gyoo et al. (2016) PDK1 Is a Regulator of Epidermal Differentiation that Activates and Organizes Asymmetric Cell Division. Cell Rep 15:1615-23
Johnson, Dylan; Mathur, Mohit C; Kobayashi, Tomoyoshi et al. (2016) The Cardiomyopathy Mutation, R146G Troponin I, Stabilizes the Intermediate ""C"" State of Regulated Actin under High- and Low-Free Ca(2+) Conditions. Biochemistry 55:4533-40
Shinkuma, Satoru; Guo, Zongyou; Christiano, Angela M (2016) Site-specific genome editing for correction of induced pluripotent stem cells derived from dominant dystrophic epidermolysis bullosa. Proc Natl Acad Sci U S A 113:5676-81
Kim, Arianna L; Back, Jung Ho; Zhu, Yucui et al. (2016) AKT1 Activation is Obligatory for Spontaneous BCC Tumor Growth in a Murine Model that Mimics Some Features of Basal Cell Nevus Syndrome. Cancer Prev Res (Phila) 9:794-802

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