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020 ▼a 9780438125902
035 ▼a (MiAaPQ)AAI10902984
035 ▼a (MiAaPQ)umichrackham:001101
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 247004
0820 ▼a 616.01
1001 ▼a Ting, Hung-An.
24510 ▼a Notch Ligand Delta-like 4 (Dll4) Induces Epigenetic Mechanism in Regulatory T Cell Function During Pulmonary Viral Infection.
260 ▼a [S.l.]: ▼b University of Michigan., ▼c 2018.
260 1 ▼a Ann Arbor: ▼b ProQuest Dissertations & Theses, ▼c 2018.
300 ▼a 152 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
500 ▼a Adviser: Nicholas W. Lukacs.
5021 ▼a Thesis (Ph.D.)--University of Michigan, 2018.
520 ▼a Respiratory Syncytial Virus (RSV) infects more than 90% of children under two years of age. It is the number one leading cause of hospitalizations for infants and young children. Inpatients suffer from RSV-induced moderate to severe bronchioliti
520 ▼a The current dissertation demonstrates that Dll4 was up-regulated by RSV infection especially on CD11b+ pulmonary dendritic cells (DC). Using systemic Dll4 neutralization and a Dll4 knockdown DC transfer model, we found that Dll4 enhanced Foxp3 e
520 ▼a Using an epigenetic enzyme PCR array, we found that Dll4 and Notch signaling enhanced the expression of a novel histone methyltransferase-SET and MYND domain containing protein 3 (SMYD3) in vitro and in vivo during RSV infection. SMYD3 catalyze
520 ▼a Collectively, the studies in this dissertation suggest that Notch and its ligand Dll4 augment immunomodulatory Treg cell programs to ameliorate RSV immunopathology in part through an epigenetic mechanism-SMYD3. The results presented herein lay t
590 ▼a School code: 0127.
650 4 ▼a Pathology.
690 ▼a 0571
71020 ▼a University of Michigan. ▼b Molecular and Cellular Pathology.
7730 ▼t Dissertation Abstracts International ▼g 79-12B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0127
791 ▼a Ph.D.
792 ▼a 2018
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T15000492 ▼n KERIS ▼z 이 자료의 원문은 한국교육학술정보원에서 제공합니다.
980 ▼a 201812 ▼f 2019
990 ▼a ***1012033