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020 ▼a 9780438310261
035 ▼a (MiAaPQ)AAI10970789
035 ▼a (MiAaPQ)OhioLINK:osu1468501949
040 ▼a MiAaPQ ▼c MiAaPQ ▼d 248032
0820 ▼a 616
1001 ▼a Church, Jamie Stoddard.
24510 ▼a Toll-like Receptor 4 Regulates Intraspinal and Peripheral Responses after Spinal Cord Injury.
260 ▼a [S.l.] : ▼b The Ohio State University., ▼c 2016
260 1 ▼a Ann Arbor : ▼b ProQuest Dissertations & Theses, ▼c 2016
300 ▼a 256 p.
500 ▼a Source: Dissertation Abstracts International, Volume: 80-01(E), Section: B.
500 ▼a Adviser: Dana McTigue.
5021 ▼a Thesis (Ph.D.)--The Ohio State University, 2016.
520 ▼a Traumatic spinal cord injury (SCI) disrupts not only tissue within the central nervous system (CNS), but homeostatic processes in the periphery as well. Macrophages are immune cells that accumulate in the spinal cord lesion site and in periphera
520 ▼a In the damaged spinal cord DAMPs initiate secondary injury processes including apoptosis and inflammation. Acutely, cells of the oligodendrocyte (OL) lineage (OLs and their progenitor cells, OPCs) are lost, but this extensive glial cell loss is
520 ▼a Anemia and pressure ulcers are two common iron-related comorbidities with SCI. Because TLR4 is an innate immune receptor and its signaling in macrophages regulates systemic iron during pathogen invasion we investigated whether TLR4 signaling inf
520 ▼a In conclusion, my graduate work shows that intraspinal TLR4 signaling alters macrophage iron regulation and myelin debris phagocytosis, and influences each stage of OL lineage cell progression in the healthy adult CNS and/or after SCI and lysole
590 ▼a School code: 0168.
650 4 ▼a Neurosciences.
650 4 ▼a Immunology.
690 ▼a 0317
690 ▼a 0982
71020 ▼a The Ohio State University. ▼b Neuroscience.
7730 ▼t Dissertation Abstracts International ▼g 80-01B(E).
773 ▼t Dissertation Abstract International
790 ▼a 0168
791 ▼a Ph.D.
792 ▼a 2016
793 ▼a English
85640 ▼u http://www.riss.kr/pdu/ddodLink.do?id=T15001367 ▼n KERIS
980 ▼a 201812 ▼f 2019
990 ▼a 관리자