<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-21T11:46:56Z</responseDate><request verb="GetRecord" identifier="oai:wakespace.lib.wfu.edu:10339/38589" metadataPrefix="dim">https://wakespace.lib.wfu.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:null:10339/38589</identifier><datestamp>2026-09-18T10:55:11Z</datestamp><setSpec>com_10339_14934</setSpec><setSpec>col_10339_38132</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">MacArthur, Philip Scott</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2013-06-06T21:19:41Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2015-06-06T08:30:09Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2013</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://wakespace.lib.wfu.edu/handle/10339/38589</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Microsomal triglyceride transfer protein (MTP) is a multifunctional protein necessary for conversion of apolipoprotein B into precursor lipoproteins and bulk triglyceride (TG) movement into the endoplasmic reticulum (ER) for precursor lipoprotein expansion. Invertebrate forms of MTP (e.g. Drosophila; dMTP) are capable of phospholipid (PL) transfer, whereas vertebrate forms (e.g. human; hMTP) engage in PL and TG transfer. We hypothesized that PL transfer is the primordial activity of MTP necessary for precursor lipoprotein particle formation, whereas TG transfer is a vertebrate adaptation necessary for trafficking of TG into the ER for 2nd-step assembly. Hence, we assessed hMTP&amp;apos;s ability to promote TG trafficking into the ER of transiently transfected or stable, Dox-inducible, non-hepatic cell lines. In cell lines that expressed hMTP, a 2.5 - 5.0-fold increase in microsomal TG content was observed. The lipid-transfer activity of MTP was necessary for this function as in the presence of a potent MTP inhibitor, BMS-212122, microsomal TG content was similar to mock-transfected cells. To determine if the TG-transfer activity of MTP facilitated TG translocation we compared the TG content of microsomes from hMTP and dMTP expressing cells. Compared to mock-transfected cells, hMTP increased microsomal TG content by ~2.5-fold while cells transfected with dMTP demonstrated no increase in microsomal TG content. These data indicate that MTP promotes TG trafficking into the ER and that the TG-transfer activity of MTP is essential for this function.</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">en</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Wake Forest University</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">ApoB</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">ER</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">LLTP</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">MTP</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Triglyceride</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">VLDL assembly</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">THE IMPACT OF MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN ON INTRACELLULAR HEPATIC NEUTRAL LIPID DISTRIBUTION AND TRAFFICKING</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Dissertation</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeChair" lang="en_US">Shelness, Gregory S.</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Dawson, Paul A.</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Parks, Griffith D.</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Parks, John S.</dim:field>
   <dim:field mdschema="thesis" element="contributor" qualifier="committeeMember" lang="en_US">Temel, Ryan E.</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="discipline" lang="en_US">Molecular Pathology</dim:field>
   <dim:field mdschema="thesis" element="embargo" qualifier="terms" lang="en_US">2015-06-06</dim:field>
   <dim:field mdschema="others" element="access-status">open.access</dim:field>
</dim:dim>
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