Immunorthodontics: in vivo gene expression of orthodontic tooth movement

被引:0
作者
Yehuda Klein
Omer Fleissig
David Polak
Yechezkel Barenholz
Ofer Mandelboim
Stella Chaushu
机构
[1] Institute of Dental Sciences,Department of Orthodontics
[2] Faculty of Dental Medicine,Department of Periodontics
[3] The Hebrew University and Hadassah Medical Center,Department of Biochemistry
[4] Faculty of Dental Medicine,undefined
[5] The Hebrew University and Hadassah Medical Center,undefined
[6] Faculty of Dental Medicine,undefined
[7] The Hebrew University and Hadassah Medical Center,undefined
[8] Lautenberg Center for Cancer Immunology,undefined
[9] Faculty of Medicine,undefined
[10] The Hebrew University and Hadassah Medical Center,undefined
[11] Institute for Medical Research Israel-Canada,undefined
[12] Hebrew University and Hadassah Medical Center,undefined
来源
Scientific Reports | / 10卷
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摘要
Orthodontic tooth movement (OTM) is a “sterile” inflammatory process. The present study aimed to reveal the underlying biological mechanisms, by studying the force associated-gene expression changes, in a time-dependent manner. Ni-Ti springs were set to move the upper 1st-molar in C57BL/6 mice. OTM was measured by μCT. Total-RNA was extracted from tissue blocks at 1,3,7 and 14-days post force application, and from two control groups: naïve and inactivated spring. Gene-expression profiles were generated by next-generation-RNA-sequencing. Gene Set Enrichment Analysis, K-means algorithm and Ingenuity pathway analysis were used for data interpretation. Genes of interest were validated with qRT-PCR. A total of 3075 differentially expressed genes (DEGs) were identified, with the greatest number at day 3. Two distinct clusters patterns were recognized: those in which DEGs peaked in the first days and declined thereafter (tissue degradation, phagocytosis, leukocyte extravasation, innate and adaptive immune system responses), and those in which DEGs were initially down-regulated and increased at day 14 (cell proliferation and migration, cytoskeletal rearrangement, tissue homeostasis, angiogenesis). The uncovering of novel innate and adaptive immune processes in OTM led us to propose a new term “Immunorthodontics”. This genomic data can serve as a platform for OTM modulation future approaches.
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