Bioinformatic Approaches for Understanding Macrophage Plasticity and Microbiome in Oral Diseases
项目来源
美国卫生和人类服务部基金(HHS)
项目主持人
FRIEDEN, LESLIE A
项目受资助机构
STATE UNIVERSITY OF NEW YORK AT BUFFALO
立项年度
2020
立项时间
未公开
项目编号
1K18DE029526-01
项目级别
国家级
研究期限
未知 / 未知
受资助金额
94393.00美元
学科
Aging; Dental/Oral and Craniofacial Disease; Genetics; Human Genome; Infectious Diseases; Microbiome;
学科代码
未公开
基金类别
Other Research Related
关键词
未公开
参与者
KIRKWOOD, KEITH L
参与机构
NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH
项目标书摘要:PROJECT SUMMARY Research: With advancing age, the immune system undergoes dynamic changes characterized by both impairment of adaptive immunity and activation of low-grade chronic inflammation. This chronic activation of inflammation associated with aging or `inflammaging'. Tristetraprolin (TTP) is an RNA binding protein that post- translationally binds to adenylate-uridylate?rich elements in the 3?-UTR of target mRNAs (including key pro- inflammatory mRNAs e.g. TNF?, COX-2 and IL-6) to promote their rapid turnover. Importantly, the project laboratory has demonstrated that failure to regulate expression of cytokines at the posttranscriptional level contributes to chronic inflammation and spontaneous alveolar bone loss with age in TTP-/- mice compared to age/sex match controls. Thus, TTP expression appears to be essential for alveolar bone homeostasis in an age- dependent manner. Data in this application and recently published data strongly support the concept that macrophages and myeloid-derived suppressor cell (MDSC) populations are expanded with age in TTP-/- mice, with concomitant reduction in lymphocyte populations. Taken together, these results support the notion that TTP may be a critical intrinsic factor of inflammaging and myeloid lineage expansion/differentiation that contributes towards skeletal homeostasis. For this K18 application, it is proposed to use data sets generated already under 5R01DE028258, to examine the role of the microbiome in contributing towards the TTP null hyperinflammatory phenotype and understand if MDSC populations from oral and non-oral sources have different expression profiles by single cell RNA sequencing. Fellowship training plan/environment: The applicant has assembled a strong mentoring team who have a long history of working together and training scientists to become successful independent investigators. The proposed project will allow the applicant to integrate his translation research portfolio with bioinformatics, which will foster the perspectives and skills necessary to continue to be a successful oral biologist.