{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/121315"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/121315","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Characterization of intestinal small heterodimer partner and farnesoid X receptor in bile acid and lipid metabolism","abstract":"Submission published under a 24 month embargo labeled 'U of I Access', the embargo will last until 2025-08-01","abstract_html":"Submission published under a 24 month embargo labeled 'U of I Access', the embargo will last until 2025-08-01","abstract_has_math":false,"creators":["Nguyễn, James Thiêntoàn"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Molecular & Integrative Physi","degree_department":null,"school":null,"contributors":["Anakk, Sayeepriyadarshini","Gaskins, Rex","Nelson, Erik R","Wang, Bo"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2023,"date_issued":"2023-08","date_published":"2023-08","updated_at":"2026-07-22T22:24:57Z","subjects":["Small Intestine","Nuclear Receptors","Farnesoid X Receptor","Fxr","Nr1h4","Small Heterodimer Partner","Nr0b2","Shp","Bile Acid","Lipid","Metabolism","Circadian"],"languages":["en","eng"],"rights":["Copyright 2023 James Nguyễn"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://hdl.handle.net/2142/121315","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Anakk, Sayeepriyadarshini","Gaskins, Rex","Nelson, Erik R","Wang, Bo"]},{"key":"dc:creator","label":"Author","values":["Nguyễn, James Thiêntoàn"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2023-08","2023-07-05"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Molecular & Integrative Physi"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Small Intestine","Nuclear Receptors","Farnesoid X Receptor","Fxr","Nr1h4","Small Heterodimer Partner","Nr0b2","Shp","Bile Acid","Lipid","Metabolism","Circadian"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["en","eng"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright 2023 James Nguyễn"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://hdl.handle.net/2142/121315"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Submission published under a 24 month embargo labeled 'U of I Access', the embargo will last until 2025-08-01","The student, James Nguyễn, accepted the attached license on 2023-06-21 at 11:48.","The student, James Nguyễn, submitted this Dissertation for approval on 2023-06-21 at 11:58.","This Dissertation was approved for publication on 2023-07-05 at 15:20.","DSpace SAF Submission Ingestion Package generated from Vireo submission #19444 on 2023-12-04 at 17:18:04","Bile acids (BAs) facilitate the digestion and absorption of dietary fats and fat-soluble vitamins through emulsification. This process helps break down fats into fatty acids for easier absorption. In addition, BAs can act as ligands for receptors that can coordinate a wide range of biological processes, such as cell proliferation and differentiation, immune response, and lipid metabolism. Farnesoid X receptor (FXR) and small heterodimer partner (SHP) are nuclear receptors, a superfamily of transcription factors important for maintaining BA homeostasis. Although there have been decades of extensive research on the regulation of bile acids through the FXR-SHP axis, intestine-specific studies are still lacking. Therefore, this dissertation is focused on (i) understanding the intestine-specific role of FXR and SHP in bile acid and lipid metabolism and (ii) how nutritional excess or stress may influence the crosstalk between the intestine and liver. Intestine-specific Shp knockout (IShpKO) mice were newly generated to study bile acid metabolism, therefore in Chapter 2, I found how short-term high cholic acid diet can lead to acute changes in the IShpKO mice before the onset of adaptation. In Chapter 3, I investigated the BA and lipid metabolic response after 4-weeks of high-fat diet in mice lacking intestinal FXR and/or SHP. I showed that the liver and small intestine gene expression relating to BA, lipid, inflammation, and barrier function were altered and, moreover, the changes within the small intestine occurred in a region-specific manner. Also, the diet and genotype affected the serum and liver bile acid composition. Lastly, in Chapter 4, my preliminary data showed circadian changes in the Shp gene expression throughout the small intestine. We hope to assess if the absence of intestinal SHP can affect other rhythmic and metabolic genes throughout the day and night. Together, these results show that intestinal FXR and SHP can potentially coordinate or individually regulate different aspects of BA and lipid metabolism and, in turn, can also affect overall health."]},{"key":"dc:format","label":"Dc Format","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["Characterization of intestinal small heterodimer partner and farnesoid X receptor in bile acid and lipid metabolism"]}]}],"canonical_facts":{"dc:contributor":["Anakk, Sayeepriyadarshini","Gaskins, Rex","Nelson, Erik R","Wang, Bo"],"dc:creator":["Nguyễn, James Thiêntoàn"],"dc:date":["2023-08","2023-07-05"],"dc:description":["Submission published under a 24 month embargo labeled 'U of I Access', the embargo will last until 2025-08-01","The student, James Nguyễn, accepted the attached license on 2023-06-21 at 11:48.","The student, James Nguyễn, submitted this Dissertation for approval on 2023-06-21 at 11:58.","This Dissertation was approved for publication on 2023-07-05 at 15:20.","DSpace SAF Submission Ingestion Package generated from Vireo submission #19444 on 2023-12-04 at 17:18:04","Bile acids (BAs) facilitate the digestion and absorption of dietary fats and fat-soluble vitamins through emulsification. This process helps break down fats into fatty acids for easier absorption. In addition, BAs can act as ligands for receptors that can coordinate a wide range of biological processes, such as cell proliferation and differentiation, immune response, and lipid metabolism. Farnesoid X receptor (FXR) and small heterodimer partner (SHP) are nuclear receptors, a superfamily of transcription factors important for maintaining BA homeostasis. Although there have been decades of extensive research on the regulation of bile acids through the FXR-SHP axis, intestine-specific studies are still lacking. Therefore, this dissertation is focused on (i) understanding the intestine-specific role of FXR and SHP in bile acid and lipid metabolism and (ii) how nutritional excess or stress may influence the crosstalk between the intestine and liver. Intestine-specific Shp knockout (IShpKO) mice were newly generated to study bile acid metabolism, therefore in Chapter 2, I found how short-term high cholic acid diet can lead to acute changes in the IShpKO mice before the onset of adaptation. In Chapter 3, I investigated the BA and lipid metabolic response after 4-weeks of high-fat diet in mice lacking intestinal FXR and/or SHP. I showed that the liver and small intestine gene expression relating to BA, lipid, inflammation, and barrier function were altered and, moreover, the changes within the small intestine occurred in a region-specific manner. Also, the diet and genotype affected the serum and liver bile acid composition. Lastly, in Chapter 4, my preliminary data showed circadian changes in the Shp gene expression throughout the small intestine. We hope to assess if the absence of intestinal SHP can affect other rhythmic and metabolic genes throughout the day and night. Together, these results show that intestinal FXR and SHP can potentially coordinate or individually regulate different aspects of BA and lipid metabolism and, in turn, can also affect overall health."],"dc:format":["application/pdf"],"dc:identifier":["https://hdl.handle.net/2142/121315"],"dc:language":["en","eng"],"dc:rights":["Copyright 2023 James Nguyễn"],"dc:subject":["Small Intestine","Nuclear Receptors","Farnesoid X Receptor","Fxr","Nr1h4","Small Heterodimer Partner","Nr0b2","Shp","Bile Acid","Lipid","Metabolism","Circadian"],"dc:title":["Characterization of intestinal small heterodimer partner and farnesoid X receptor in bile acid and lipid metabolism"],"dc:type":["text"],"thesis:degree_discipline":["Molecular & Integrative Physi"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Ph.D."],"thesis:institution_name":["University of Illinois at Urbana-Champaign"]},"updated_at":"2026-07-22T22:24:57Z"}