杰森·霍顿的头像
315 464-5540

杰森·霍顿博士.D.

3119 Institute For Human Performance (IHP)
欧文大道505号
锡拉丘兹,纽约州13210
Jason Horton's email address generated as an image

当前预约

大学助理教授 整形外科手术
大学助理教授 细胞与发育生物学
大学助理教授 放射肿瘤学

语言

英语

RESEARCH PROGRAMS AND AFFILIATIONS

生物医学科学专业
神经科学与生理学
整形外科手术

研究兴趣

骨骼发育, maturation and maintenance;  Mesenchymal stem cell biology;  Radiobiology of skeletal tissues; Radiosensitization of pediatric musculoskeletal sarcoma.

协会/会员

American Association for the Advancement of Science (AAAS)
American Society for Bone and Mineral 研究 (ASBMR)

教育

奖学金: National Institutes of Health, 2015, Craniofacial and Skeletal Development
奖学金: National Cancer Institute, NIH, Bethesda, MD, 2014, 放射肿瘤学
博士: SUNY 上州医科大学, 2011, Physiology
BS: Oswego State University, 2000, Biology, Bio-cultural Anthropology

研究抽象

骨骼发育, maturation and maintenance: The structures that form the skeleton arise very early in embryonic development, continue to grow during childhood, and are actively remodeled throughout our lives. My research in this area focuses on how intercellular signaling between bone forming osteoblasts, 骨吸收破骨细胞, hematopoietic and vascular cells, along with input from systemic endocrine stimuli, collaboratively regulate bone integrity. Perturbation of these signaling circuits can lead to variety of structural and metabolic bone diseases, 比如骨质疏松症, 并可能导致骨折. Greater understanding of signaling within this bone microenvironment may translate to new strategies to prevent or correct bone disease.

间充质干细胞生物学: Mesenchymal stem cells (MSCs) derive from the embryonic mesoderm and give rise to the connective tissues throughout the body. Lineage restricted derivatives of these cells persist through post-natal growth, and function in maintenance and repair of connective tissues throughout our life span. Whether these MSC's persist post-natally as truly, multipotent 'stem cells' is unresolved due to a lack of sufficiently specific molecular markers, which identify these cells in situ. My research in this area focuses on identifying the factors that specify differentiation of MSC and their post-natal derivatives, 朝向骨头, 软骨, 还有脂肪血统. Better understanding of the biology of these cells will enhance our ability to identify these cells, and may facilitate the use of such cells in therapeutic applications.

Radiobiology of skeletal tissues: Ionizing radiation is used in the treatment of many solid cancers, but can cause collateral damage to healthy tissues surrounding the targeted tumor. 偶尔, irradiation of skeletal structures is unavoidable, and can result in localized radiation-induced bone disease, and elevated susceptibility to atraumatic fracture. My research in this area will study the radiobiologic response of the bone microenvironment, to determine the mechanisms that result in persistent osteogenitor depletion and replacement of hematopoietic marrow with adipose tissue. The goal of this line of research is to develop strategies which prevent or repair bone damage resulting from radiation exposure, and minimize the impact of radiation-induced bone disease on the quality of life of cancer survivors.

Radiosensitization of pediatric musculoskeletal sarcoma: Sarcomas are a family of cancers that develop in connective tissues such as the muscle or bone. Ewing's sarcoma and rhabdomyosarcoma, which develop in bone and muscle respectively, are pediatric cancers with a tendency to occur adjacent to areas of active bone growth. In addition to surgery and chemotherapy, ionizing radiation is used to treat these cancers, but may result in permanent damage to growing bone including asymmetric growth arrest, angular deformity and increased susceptibility to fracture. The severity of bone injury is largely determined by the dose of radiation that the bone receives. Therefore it is reasoned that strategies which selectively sensitize tumor tissue to radiation could lower the dose of radiation needed to achieve local control, and minimize collateral injury of adjacent healthy tissue.

 

出版物

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