The Tissue Procurement Core Facility is designed as a central tissue acquisition and distribution facility which will provide tissues to all Program Project investigators. The purpose of this facility is to enable the efficient collection and use of tissues from patients undergoing surgery. The facility will combine under one umbrella, the patient contact and clinical evaluation aspects of tissue collection with the initial processing of tissues so that efforts are not duplicated by different investigators. Tissues for the Program Project will be obtained from reproductive tract organs of patients undergoing hysterectomy. The Core Facility will be responsible for identification and enrollment of patients. This function will include evaluating the appropriateness of clinical cases, overseeing informed consent, and providing the evaluation of tissue samples for endocrine condition and gross pathology. The second function of the Core Facility will be to coordinate tissue processing and distribution. This function will ensure that maximal use is made of available tissues by all investigators. The third function of this Core will include preparation of cell suspensions. Epithelial, immune cells and stromal cells will be prepared from the Fallopian tube, uterus, cervix, and vagina. In addition, Core B will be responsible for collating patient data on selected clinical parameters. This will enable investigators to evaluate hypotheses as they arise in the course of Program Project research. The Core Facility combines the expertise of its members which include a Core Director, Medical Coordinator, Microbiologist, Pathologist and Biostatistician. These individuals will provide consultation and support for all of the Core services. In addition, the Core will have the services of a Nurse Coordinator who will meet with patients, and two highly trained technicians who will participate in tissue dissection, fixation, and disruption. The biostatistical shared service at DHMC will provide consultation for the statistical evaluations to be made as part of this section.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI034478-04S1
Application #
2755628
Study Section
Project Start
Project End
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
4
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Dartmouth College
Department
Type
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
Haddad, Severina N; Wira, Charles R (2014) Estradiol regulation of constitutive and keratinocyte growth factor-induced CCL20 and CXCL1 secretion by mouse uterine epithelial cells. Am J Reprod Immunol 72:34-44
Wira, Charles R; Rossoll, Richard M; Young, Roger C (2005) Polarized uterine epithelial cells preferentially present antigen at the basolateral surface: role of stromal cells in regulating class II-mediated epithelial cell antigen presentation. J Immunol 175:1795-804
Fahey, John V; Rossoll, Richard M; Wira, Charles R (2005) Sex hormone regulation of anti-bacterial activity in rat uterine secretions and apical release of anti-bacterial factor(s) by uterine epithelial cells in culture. J Steroid Biochem Mol Biol 93:59-66
Asin, Susana N; Fanger, Michael W; Wildt-Perinic, Dunja et al. (2004) Transmission of HIV-1 by primary human uterine epithelial cells and stromal fibroblasts. J Infect Dis 190:236-45
Yeaman, Grant R; Asin, Susana; Weldon, Sally et al. (2004) Chemokine receptor expression in the human ectocervix: implications for infection by the human immunodeficiency virus-type I. Immunology 113:524-33
Yeaman, Grant R; Howell, Alexandra L; Weldon, Sally et al. (2003) Human immunodeficiency virus receptor and coreceptor expression on human uterine epithelial cells: regulation of expression during the menstrual cycle and implications for human immunodeficiency virus infection. Immunology 109:137-46
Wira, Charles R; Fahey, John V; Abrahams, Vikki M et al. (2003) Influence of stage of the reproductive cycle and estradiol on thymus cell antigen presentation. J Steroid Biochem Mol Biol 84:79-87
Wira, Charles R; Rossoll, Richard M (2003) Oestradiol regulation of antigen presentation by uterine stromal cells: role of transforming growth factor-beta production by epithelial cells in mediating antigen-presenting cell function. Immunology 109:398-406
Abrahams, Vikki M; Collins, Jane E; Wira, Charles R et al. (2003) Inhibition of human polymorphonuclear cell oxidative burst by 17-beta-estradiol and 2,3,7,8-tetrachlorodibenzo-p-dioxin. Am J Reprod Immunol 50:463-72
Wira, Charles R; Roche, Marcie A; Rossoll, Richard M (2002) Antigen presentation by vaginal cells: role of TGFbeta as a mediator of estradiol inhibition of antigen presentation. Endocrinology 143:2872-9

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