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
Glycolytic Metabolism Plays a Functi...
~
Gu, Wen.
FindBook
Google Book
Amazon
博客來
Glycolytic Metabolism Plays a Functional Role in Regulating Human Pluripotent Stem Cell State.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Glycolytic Metabolism Plays a Functional Role in Regulating Human Pluripotent Stem Cell State./
作者:
Gu, Wen.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2017,
面頁冊數:
132 p.
附註:
Source: Dissertation Abstracts International, Volume: 78-06(E), Section: B.
Contained By:
Dissertation Abstracts International78-06B(E).
標題:
Developmental biology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10255331
ISBN:
9781369532036
Glycolytic Metabolism Plays a Functional Role in Regulating Human Pluripotent Stem Cell State.
Gu, Wen.
Glycolytic Metabolism Plays a Functional Role in Regulating Human Pluripotent Stem Cell State.
- Ann Arbor : ProQuest Dissertations & Theses, 2017 - 132 p.
Source: Dissertation Abstracts International, Volume: 78-06(E), Section: B.
Thesis (Ph.D.)--University of California, Los Angeles, 2017.
The rate of glycolytic metabolism changes during differentiation of human embryonic stem cells (hESCs) and reprogramming of somatic cells to pluripotent stem cells. However, the functional contribution of glycolytic metabolism to pluripotency is unclear. Here we show that the degree of pluripotency is associated with glycolytic rate, whereby naive hESCs exhibit increased glycolytic flux, MYC transcriptional activity, and nuclear localization of N-MYC relative to primed hESCs. This is consistent with the inner cell mass of human blastocysts which exhibit increased MYC transcriptional activity relative primed hESCs and elevated nuclear N-MYC levels. Reduction of glycolysis decreases self-renewal of naive hESCs and feeder-free cultured primed hESCs, but not primed hESCs grown in feeder-supported conditions. Reduction of glycolysis in feeder-free primed hESCs also enhances neural specification. These findings reveal associations between glycolytic metabolism and the state of pluripotency, differences in the metabolism of feeder- versus feeder-free cultured hESCs, and identify methods for regulating self-renewal and initial cell fate specification of hESCs.
ISBN: 9781369532036Subjects--Topical Terms:
592588
Developmental biology.
Glycolytic Metabolism Plays a Functional Role in Regulating Human Pluripotent Stem Cell State.
LDR
:02139nmm a2200301 4500
001
2124070
005
20171023101707.5
008
180830s2017 ||||||||||||||||| ||eng d
020
$a
9781369532036
035
$a
(MiAaPQ)AAI10255331
035
$a
AAI10255331
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Gu, Wen.
$3
3286043
245
1 0
$a
Glycolytic Metabolism Plays a Functional Role in Regulating Human Pluripotent Stem Cell State.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2017
300
$a
132 p.
500
$a
Source: Dissertation Abstracts International, Volume: 78-06(E), Section: B.
500
$a
Adviser: Heather R. Christofk.
502
$a
Thesis (Ph.D.)--University of California, Los Angeles, 2017.
520
$a
The rate of glycolytic metabolism changes during differentiation of human embryonic stem cells (hESCs) and reprogramming of somatic cells to pluripotent stem cells. However, the functional contribution of glycolytic metabolism to pluripotency is unclear. Here we show that the degree of pluripotency is associated with glycolytic rate, whereby naive hESCs exhibit increased glycolytic flux, MYC transcriptional activity, and nuclear localization of N-MYC relative to primed hESCs. This is consistent with the inner cell mass of human blastocysts which exhibit increased MYC transcriptional activity relative primed hESCs and elevated nuclear N-MYC levels. Reduction of glycolysis decreases self-renewal of naive hESCs and feeder-free cultured primed hESCs, but not primed hESCs grown in feeder-supported conditions. Reduction of glycolysis in feeder-free primed hESCs also enhances neural specification. These findings reveal associations between glycolytic metabolism and the state of pluripotency, differences in the metabolism of feeder- versus feeder-free cultured hESCs, and identify methods for regulating self-renewal and initial cell fate specification of hESCs.
590
$a
School code: 0031.
650
4
$a
Developmental biology.
$3
592588
650
4
$a
Biochemistry.
$3
518028
650
4
$a
Cellular biology.
$3
3172791
690
$a
0758
690
$a
0487
690
$a
0379
710
2
$a
University of California, Los Angeles.
$b
Molecular and Medical Pharmacology.
$3
3286001
773
0
$t
Dissertation Abstracts International
$g
78-06B(E).
790
$a
0031
791
$a
Ph.D.
792
$a
2017
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10255331
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
W9334682
電子資源
01.外借(書)_YB
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