Language:
English
繁體中文
Help
回圖書館首頁
手機版館藏查詢
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
Regulatory Roles of Adipocyte Glucoc...
~
Amatya, Shripa.
Linked to FindBook
Google Book
Amazon
博客來
Regulatory Roles of Adipocyte Glucocorticoid Receptor Signaling in Adipose Tissue.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Regulatory Roles of Adipocyte Glucocorticoid Receptor Signaling in Adipose Tissue./
Author:
Amatya, Shripa.
Published:
Ann Arbor : ProQuest Dissertations & Theses, : 2023,
Description:
198 p.
Notes:
Source: Dissertations Abstracts International, Volume: 85-06, Section: B.
Contained By:
Dissertations Abstracts International85-06B.
Subject:
Physiology. -
Online resource:
https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30813729
ISBN:
9798380945189
Regulatory Roles of Adipocyte Glucocorticoid Receptor Signaling in Adipose Tissue.
Amatya, Shripa.
Regulatory Roles of Adipocyte Glucocorticoid Receptor Signaling in Adipose Tissue.
- Ann Arbor : ProQuest Dissertations & Theses, 2023 - 198 p.
Source: Dissertations Abstracts International, Volume: 85-06, Section: B.
Thesis (Ph.D.)--Louisiana State University Health Sciences Center - Shreveport, 2023.
Glucocorticoids acting via the glucocorticoid receptors (GR) are known to be key regulators of metabolism and stress response. However, uncontrolled, or excess GR signaling adversely can inflame adipose tissue to impact function of systemic endocrine, immune, and metabolic systems. Adipose tissue inflammation promotes systemic metabolic dysfunctions; however, the molecular mechanisms underlying the role of adipocyte GR in the regulation of genes associated with adipose tissue inflammation remain poorly understood. We performed in vivo studies using adipocyte-specific GR knockout mice (Adipo GRKO) in conjunction with in vitro studies to understand the contribution of adipocyte GR in regulating adipose tissue immune homeostasis. To examine the effect of systemic stress signaling on immune regulatory gene expression in adipose tissue, we performed studies where mice underwent acute psychogenic stress. We used both male and female mice to observe potential sex differences in adipocyte GR regulation of adipose tissue functions. Our findings showed that adipocyte specific GR signaling regulated adipokines at both mRNA and plasma levels, and immune regulatory (Coch, Pdcd1, Cemip, Cxcr2, Tnfa, Il6, and Il12a) mRNA gene expression, which affected myeloid immune cell presence in white adipose tissue. We found that in adipocytes, GR directly downregulated Cxcr2 whereas in non-adipocytes or stromal cells, adipocyte GR indirectly affected Pdcd1, Cemip and Il6 gene expression. Our findings suggest that adipocyte GR signaling suppresses inflammatory signals, maintaining immune homeostasis. We also found sex-specific differences in GR signaling in adipose tissue in response to stress. Elucidating physiological roles of adipocyte GR in maintaining endocrine, immune and metabolic homeostasis in adipose tissue will help explain pathologies associated with adipose tissue dysfunction.
ISBN: 9798380945189Subjects--Topical Terms:
518431
Physiology.
Subjects--Index Terms:
Acute stress
Regulatory Roles of Adipocyte Glucocorticoid Receptor Signaling in Adipose Tissue.
LDR
:03161nmm a2200421 4500
001
2401146
005
20241015112543.5
006
m o d
007
cr#unu||||||||
008
251215s2023 ||||||||||||||||| ||eng d
020
$a
9798380945189
035
$a
(MiAaPQ)AAI30813729
035
$a
AAI30813729
035
$a
2401146
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Amatya, Shripa.
$3
3771214
245
1 0
$a
Regulatory Roles of Adipocyte Glucocorticoid Receptor Signaling in Adipose Tissue.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2023
300
$a
198 p.
500
$a
Source: Dissertations Abstracts International, Volume: 85-06, Section: B.
500
$a
Advisor: Cruz-Topete, Diana.
502
$a
Thesis (Ph.D.)--Louisiana State University Health Sciences Center - Shreveport, 2023.
520
$a
Glucocorticoids acting via the glucocorticoid receptors (GR) are known to be key regulators of metabolism and stress response. However, uncontrolled, or excess GR signaling adversely can inflame adipose tissue to impact function of systemic endocrine, immune, and metabolic systems. Adipose tissue inflammation promotes systemic metabolic dysfunctions; however, the molecular mechanisms underlying the role of adipocyte GR in the regulation of genes associated with adipose tissue inflammation remain poorly understood. We performed in vivo studies using adipocyte-specific GR knockout mice (Adipo GRKO) in conjunction with in vitro studies to understand the contribution of adipocyte GR in regulating adipose tissue immune homeostasis. To examine the effect of systemic stress signaling on immune regulatory gene expression in adipose tissue, we performed studies where mice underwent acute psychogenic stress. We used both male and female mice to observe potential sex differences in adipocyte GR regulation of adipose tissue functions. Our findings showed that adipocyte specific GR signaling regulated adipokines at both mRNA and plasma levels, and immune regulatory (Coch, Pdcd1, Cemip, Cxcr2, Tnfa, Il6, and Il12a) mRNA gene expression, which affected myeloid immune cell presence in white adipose tissue. We found that in adipocytes, GR directly downregulated Cxcr2 whereas in non-adipocytes or stromal cells, adipocyte GR indirectly affected Pdcd1, Cemip and Il6 gene expression. Our findings suggest that adipocyte GR signaling suppresses inflammatory signals, maintaining immune homeostasis. We also found sex-specific differences in GR signaling in adipose tissue in response to stress. Elucidating physiological roles of adipocyte GR in maintaining endocrine, immune and metabolic homeostasis in adipose tissue will help explain pathologies associated with adipose tissue dysfunction.
590
$a
School code: 0786.
650
4
$a
Physiology.
$3
518431
650
4
$a
Genetics.
$3
530508
650
4
$a
Cellular biology.
$3
3172791
650
4
$a
Molecular biology.
$3
517296
653
$a
Acute stress
653
$a
Adipocyte
653
$a
Adipokine
653
$a
Glucocorticoid receptors
653
$a
Homeostasis
653
$a
Immune homeostasis
690
$a
0719
690
$a
0369
690
$a
0379
690
$a
0307
710
2
$a
Louisiana State University Health Sciences Center - Shreveport.
$b
Molecular and Cellular Physiology.
$3
3771215
773
0
$t
Dissertations Abstracts International
$g
85-06B.
790
$a
0786
791
$a
Ph.D.
792
$a
2023
793
$a
English
856
4 0
$u
https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30813729
based on 0 review(s)
Location:
ALL
電子資源
Year:
Volume Number:
Items
1 records • Pages 1 •
1
Inventory Number
Location Name
Item Class
Material type
Call number
Usage Class
Loan Status
No. of reservations
Opac note
Attachments
W9509466
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
On shelf
0
1 records • Pages 1 •
1
Multimedia
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login