The goals of the Columbia University Medical Center Skin Disease Research Center are to understand the developmental biology of the skin, and to understand the pathogenic interactions between immune cells and target cells in the skin in humans. These goals require sophisticated processing and analysis of primary human tissues and blood. Since these materials are precious and cell yields are small, it is essential to bring the greatest analytic capacity to bear on each human tissue sample. The Immunophenotype Core (IPC) takes advantage of the ongoing experience of the Clynes and Sykes labs, in applying basic immunological research to translational questions in human diseases to now focus this expertise on inflammatory diseases of the skin. Flow cytometry has become the primary tool for the identification of cell populations according to specific parameters, and is therefore employed by an ever-growing number of biomedical scientists. The ability to design, perform and analyze data from multi-parametric flow cytometric experiments requires technical expertise but also immunological expertise to appropriately design the experiment. The method is technologically complex and the equipment is expensive, necessitating shared instrumentation amongst groups of users to facilitate expert use and availability of these vital and versatile instruments. In the next five years, together with our colleagues in the SDRCCUMC, flow cytometric analysis and sorting strategies will 1) define the inflammatory response in alopecia, specifically the NKG2D positive CDS T cell population in the human and mouse;2) isolate relevant cutaneous rare cellular populations for functional studies (Merkel, epithelial stem cell, myeloid suppressor cells, and 3) analyse phenotypic consequences of skin perturbations on cellular function.

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 #
8499259
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
$155,356
Indirect Cost
$58,860
Name
Columbia University (N.Y.)
Department
Type
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Shen, Yao; Stanislauskas, Milda; Li, Gen et al. (2017) Epigenetic and genetic dissections of UV-induced global gene dysregulation in skin cells through multi-omics analyses. Sci Rep 7:42646
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
Sun, Xiaoyun; Kim, Arianna; Nakatani, Masashi et al. (2016) Distinctive molecular responses to ultraviolet radiation between keratinocytes and melanocytes. Exp Dermatol 25:708-13
Marshall, Kara L; Clary, Rachel C; Baba, Yoshichika et al. (2016) Touch Receptors Undergo Rapid Remodeling in Healthy Skin. Cell Rep 17:1719-1727
Mackay-Wiggan, Julian; Jabbari, Ali; Nguyen, Nhan et al. (2016) Oral ruxolitinib induces hair regrowth in patients with moderate-to-severe alopecia areata. JCI Insight 1:e89790
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
Abaci, Hasan E; Guo, Zongyou; Coffman, Abigail et al. (2016) Human Skin Constructs with Spatially Controlled Vasculature Using Primary and iPSC-Derived Endothelial Cells. Adv Healthc Mater 5:1800-7

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