語系:
繁體中文
English
說明(常見問題)
回圖書館首頁
手機版館藏查詢
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
The signals that regulate cytokine p...
~
Nagarajan, Niranjana Aditi.
FindBook
Google Book
Amazon
博客來
The signals that regulate cytokine production by natural killer T cells.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
The signals that regulate cytokine production by natural killer T cells./
作者:
Nagarajan, Niranjana Aditi.
面頁冊數:
192 p.
附註:
Source: Dissertation Abstracts International, Volume: 66-08, Section: B, page: 4150.
Contained By:
Dissertation Abstracts International66-08B.
標題:
Health Sciences, Immunology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3187820
ISBN:
9780542293580
The signals that regulate cytokine production by natural killer T cells.
Nagarajan, Niranjana Aditi.
The signals that regulate cytokine production by natural killer T cells.
- 192 p.
Source: Dissertation Abstracts International, Volume: 66-08, Section: B, page: 4150.
Thesis (Ph.D.)--University of California, San Diego, 2005.
Natural Killer T (NKT) cells influence many immune processes through the production of cytokines, and the research described in this dissertation is directed towards elucidating the signals that regulate cytokine production by these cells. Antigen presentation is a known regulator of T cell responses and the requirements for CD1d-mediated antigen presentation were investigated. These studies demonstrate that CD1d requires lysosomal trafficking in order to present glycosphingolipid (GSL) antigens to NKT cells, and that this trafficking is mediated by the interaction of the cytoplasmic tail of CD1d with the adaptor protein complex AP-3. The nature of the GSL antigen used is also known to affect NKT cell cytokine production, and structurally modified altered glycolipid ligands were used to characterize effect of altering antigen avidity and affinity on cytokine production. The model antigen used to stimulate NKT cells, alpha-galactosylceramide (alphaGalCer), induces an unbiased TH0 response, with equivalent production of interferon-gamma (IFNgamma) and interleukin (IL)-4 by these cells. OCH, a variant of alphaGalCer that induces a TH2-biased systemic response, activates NKT cells to a similar degree as alphaGalCer. The mechanism of this altered activation is unclear, as OCH induces a similar degree of early signaling as alphaGalCer although it associates with the TCR with lesser avidity, suggesting that while OCH may not alter NKT cell activation, it affects the downstream activation of other cells. C-glycoside, a variant of alphaGalCer that induces a TH1-biased response, is a poor early activator of NKT cells, inducing low early signaling and binding the TCR with low affinity and avidity, probably inducing low, sustained signaling that results in a systemic TH1 response. These studies also demonstrate that NKT cells respond to bacterial lipopolysaccharide (LPS), and that their response to LPS is polarized, with exclusively IFNgamma and no IL-4 being produced. NKT cells do not express toll-like receptor-4 and respond indirectly, to IL-12 and IL-18 produced in response to LPS. NKT cells are also critical for the systemic response to LPS, and mice that are genetically deficient for NKT cells exhibit severely impaired production of pro-inflammatory cytokines.
ISBN: 9780542293580Subjects--Topical Terms:
1017716
Health Sciences, Immunology.
The signals that regulate cytokine production by natural killer T cells.
LDR
:03280nmm 2200301 4500
001
1826118
005
20061218074246.5
008
130610s2005 eng d
020
$a
9780542293580
035
$a
(UnM)AAI3187820
035
$a
AAI3187820
040
$a
UnM
$c
UnM
100
1
$a
Nagarajan, Niranjana Aditi.
$3
1915090
245
1 4
$a
The signals that regulate cytokine production by natural killer T cells.
300
$a
192 p.
500
$a
Source: Dissertation Abstracts International, Volume: 66-08, Section: B, page: 4150.
500
$a
Chairs: Mitchell Kronenberg; Suresh Subramani.
502
$a
Thesis (Ph.D.)--University of California, San Diego, 2005.
520
$a
Natural Killer T (NKT) cells influence many immune processes through the production of cytokines, and the research described in this dissertation is directed towards elucidating the signals that regulate cytokine production by these cells. Antigen presentation is a known regulator of T cell responses and the requirements for CD1d-mediated antigen presentation were investigated. These studies demonstrate that CD1d requires lysosomal trafficking in order to present glycosphingolipid (GSL) antigens to NKT cells, and that this trafficking is mediated by the interaction of the cytoplasmic tail of CD1d with the adaptor protein complex AP-3. The nature of the GSL antigen used is also known to affect NKT cell cytokine production, and structurally modified altered glycolipid ligands were used to characterize effect of altering antigen avidity and affinity on cytokine production. The model antigen used to stimulate NKT cells, alpha-galactosylceramide (alphaGalCer), induces an unbiased TH0 response, with equivalent production of interferon-gamma (IFNgamma) and interleukin (IL)-4 by these cells. OCH, a variant of alphaGalCer that induces a TH2-biased systemic response, activates NKT cells to a similar degree as alphaGalCer. The mechanism of this altered activation is unclear, as OCH induces a similar degree of early signaling as alphaGalCer although it associates with the TCR with lesser avidity, suggesting that while OCH may not alter NKT cell activation, it affects the downstream activation of other cells. C-glycoside, a variant of alphaGalCer that induces a TH1-biased response, is a poor early activator of NKT cells, inducing low early signaling and binding the TCR with low affinity and avidity, probably inducing low, sustained signaling that results in a systemic TH1 response. These studies also demonstrate that NKT cells respond to bacterial lipopolysaccharide (LPS), and that their response to LPS is polarized, with exclusively IFNgamma and no IL-4 being produced. NKT cells do not express toll-like receptor-4 and respond indirectly, to IL-12 and IL-18 produced in response to LPS. NKT cells are also critical for the systemic response to LPS, and mice that are genetically deficient for NKT cells exhibit severely impaired production of pro-inflammatory cytokines.
590
$a
School code: 0033.
650
4
$a
Health Sciences, Immunology.
$3
1017716
650
4
$a
Biology, Cell.
$3
1017686
650
4
$a
Biology, Animal Physiology.
$3
1017835
690
$a
0982
690
$a
0379
690
$a
0433
710
2 0
$a
University of California, San Diego.
$3
1018093
773
0
$t
Dissertation Abstracts International
$g
66-08B.
790
1 0
$a
Kronenberg, Mitchell,
$e
advisor
790
1 0
$a
Subramani, Suresh,
$e
advisor
790
$a
0033
791
$a
Ph.D.
792
$a
2005
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3187820
筆 0 讀者評論
館藏地:
全部
電子資源
出版年:
卷號:
館藏
1 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
借閱狀態
預約狀態
備註欄
附件
W9216981
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
評論
新增評論
分享你的心得
Export
取書館
處理中
...
變更密碼
登入