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Tales of metabolic regulation: Adipo...

Krumm, Christopher Steven.

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Tales of metabolic regulation: Adiponectin in the cow and Sel1l in the mouse.

Record Type:	Electronic resources : Monograph/item
Title/Author:	Tales of metabolic regulation: Adiponectin in the cow and Sel1l in the mouse./
Author:	Krumm, Christopher Steven.
Published:	Ann Arbor : ProQuest Dissertations & Theses, : 2017,
Description:	185 p.
Notes:	Source: Dissertation Abstracts International, Volume: 78-05(E), Section: B.
Contained By:	Dissertation Abstracts International78-05B(E).
Subject:	Animal sciences. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10250853
ISBN:	9781369437959

Tales of metabolic regulation: Adiponectin in the cow and Sel1l in the mouse.
Krumm, Christopher Steven.

Tales of metabolic regulation: Adiponectin in the cow and Sel1l in the mouse. - Ann Arbor : ProQuest Dissertations & Theses, 2017 - 185 p.

Source: Dissertation Abstracts International, Volume: 78-05(E), Section: B.

Thesis (Ph.D.)--Cornell University, 2017.

The first part of this dissertation assessed factors regulating the insulin sensitizing hormone adiponectin in dairy cows. Plasma adiponectin is reduced during the transition from late pregnancy (LP) to early lactation (EL) in parallel with rapid changes in the plasma concentration of metabolic hormones [i.e. insulin, leptin, and growth hormone (GH)] and non-esterified fatty acids (NEFA). The first study of this dissertation showed that none of these factors contribute to the regulation of plasma adiponectin. The second study tested the possibility that altered endoplasmic reticulum (ER) chaperone expression is involved. This was motivated by the following observations: 1) Plasma adiponectin variation in transition dairy cows occurs in absence of changes in adiponectin mRNA. 2) In rodents, the master regulator of ER homeostasis x-box binding protein 1 (Xbp1) regulates adiponectin production by increasing ER chaperone expression. We showed that Xbp1 expression decreased from LP to EL in the dairy cow. Using a primary bovine adipocyte system, overexpression of Xbp1 had no effect on adiponectin, despite increasing expression of several ER chaperone proteins. The factors regulating plasma adiponectin in the transition dairy cow remain unknown.

ISBN: 9781369437959Subjects--Topical Terms:

3174829
Animal sciences.

Tales of metabolic regulation: Adiponectin in the cow and Sel1l in the mouse.
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100 1 $a Krumm, Christopher Steven. $3 3286031
245 1 0 $a Tales of metabolic regulation: Adiponectin in the cow and Sel1l in the mouse.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 2017
300 $a 185 p.
500 $a Source: Dissertation Abstracts International, Volume: 78-05(E), Section: B.
500 $a Adviser: Yves R. Boisclair.
502 $a Thesis (Ph.D.)--Cornell University, 2017.
520 $a The first part of this dissertation assessed factors regulating the insulin sensitizing hormone adiponectin in dairy cows. Plasma adiponectin is reduced during the transition from late pregnancy (LP) to early lactation (EL) in parallel with rapid changes in the plasma concentration of metabolic hormones [i.e. insulin, leptin, and growth hormone (GH)] and non-esterified fatty acids (NEFA). The first study of this dissertation showed that none of these factors contribute to the regulation of plasma adiponectin. The second study tested the possibility that altered endoplasmic reticulum (ER) chaperone expression is involved. This was motivated by the following observations: 1) Plasma adiponectin variation in transition dairy cows occurs in absence of changes in adiponectin mRNA. 2) In rodents, the master regulator of ER homeostasis x-box binding protein 1 (Xbp1) regulates adiponectin production by increasing ER chaperone expression. We showed that Xbp1 expression decreased from LP to EL in the dairy cow. Using a primary bovine adipocyte system, overexpression of Xbp1 had no effect on adiponectin, despite increasing expression of several ER chaperone proteins. The factors regulating plasma adiponectin in the transition dairy cow remain unknown.
520 $a The second part of this dissertation addressed the role of sel-1 suppressor of lin-12-like protein (Sel1l) in lipid metabolism. Sel1l is a critical component of the endoplasmic reticulum associated degradation (ERAD) system required for translocation and degradation of misfolded or aggregated proteins. Adipose-specific deletion of Sel1l in mice has implicated an ERAD-independent role for Sel1l in lipid metabolism. To this end, we generated liver-specific Sel1l knockout mice (DeltaSel1lLiver) to assess whether Sel1l plays a similar role in lipid homeostasis in liver. Lipid metabolism was nearly normal in DeltaSel1l Liver mice fed chow or high fat diet. DeltaSel1lLiver mice on an atherogenic diet (AD) showed increased hyperlipidemia, hypercholesterolemia, liver damage, and occasional death compared to wildtype (WT) mice. This phenotype was associated with increased 3-hydroxy-3-methylglutaryl-CoA reductase (Hmgcr) and decreased low-density lipoprotein receptor (Ldlr) in liver of DeltaSel1l Liver mice. Together, our results reveal a previously unknown role for Sel1l in lipid homeostasis in liver, but further studies are needed to elucidate the mechanism.
590 $a School code: 0058.
650 4 $a Animal sciences. $3 3174829
650 4 $a Biology. $3 522710
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690 $a 0306
710 2 $a Cornell University. $b Animal Science. $3 3286032
773 0 $t Dissertation Abstracts International $g 78-05B(E).
790 $a 0058
791 $a Ph.D.
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793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10250853