Specific Expression of Apolipoprotein A-IV in the Follicle-Associated Epithelium of the Small Intestine

Background Peyer’s patches (PPs), which are covered by specialized follicle-associated epithelium (FAE) including M cells, play a central role in immune induction in the gastrointestinal tract. This study is to investigate a new molecule to characterize PPs. Methods We generated a monoclonal antibod...

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Veröffentlicht in:Digestive diseases and sciences 2014-11, Vol.59 (11), p.2682-2692
Hauptverfasser: Tokuhara, Daisuke, Nochi, Tomonori, Matsumura, Akiko, Mejima, Mio, Takahashi, Yuko, Kurokawa, Shiho, Kiyono, Hiroshi, Yuki, Yoshikazu
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container_end_page 2692
container_issue 11
container_start_page 2682
container_title Digestive diseases and sciences
container_volume 59
creator Tokuhara, Daisuke
Nochi, Tomonori
Matsumura, Akiko
Mejima, Mio
Takahashi, Yuko
Kurokawa, Shiho
Kiyono, Hiroshi
Yuki, Yoshikazu
description Background Peyer’s patches (PPs), which are covered by specialized follicle-associated epithelium (FAE) including M cells, play a central role in immune induction in the gastrointestinal tract. This study is to investigate a new molecule to characterize PPs. Methods We generated a monoclonal antibody (mAb 10-15-3-3) that specifically reacts to the epithelium of PPs and isolated lymphoid follicles. Target antigen was analyzed by immunoprecipitation and mass spectrometry. Localization and expression of target antigen were evaluated by immunofluorescence, in situ hybridization and real-time PCR. Results Immunoprecipitation and mass spectrometry revealed that mAb 10-15-3-3 recognized apolipoprotein A-IV (ApoA-IV), a well-known lipid transporter; this finding was confirmed by the specific reactivity of mAb 10-15-3-3 to cells transfected with the murine ApoA-IV gene. Immunofluorescence using mAb 10-15-3-3 showed intestinal localization of ApoA-IV, in which strong expression of the ApoA-IV protein occurred throughout the entire intestinal epithelium during developing period before weaning but was restricted to the FAE in adult mice. In support of these findings, in situ hybridization showed strong expression of the ApoA-IV gene throughout the entire intestinal epithelium during developing period before weaning, but this expression was restricted to the FAE predominantly and the tips of villi to a lesser extent in adult mice. Deficiency of ApoA-IV had no effect on the organogenesis of PP in mice. Conclusions Our current results reveal ApoA-IV as a novel FAE-specific marker especially in the upper small intestine of adult mice.
doi_str_mv 10.1007/s10620-014-3203-6
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This study is to investigate a new molecule to characterize PPs. Methods We generated a monoclonal antibody (mAb 10-15-3-3) that specifically reacts to the epithelium of PPs and isolated lymphoid follicles. Target antigen was analyzed by immunoprecipitation and mass spectrometry. Localization and expression of target antigen were evaluated by immunofluorescence, in situ hybridization and real-time PCR. Results Immunoprecipitation and mass spectrometry revealed that mAb 10-15-3-3 recognized apolipoprotein A-IV (ApoA-IV), a well-known lipid transporter; this finding was confirmed by the specific reactivity of mAb 10-15-3-3 to cells transfected with the murine ApoA-IV gene. Immunofluorescence using mAb 10-15-3-3 showed intestinal localization of ApoA-IV, in which strong expression of the ApoA-IV protein occurred throughout the entire intestinal epithelium during developing period before weaning but was restricted to the FAE in adult mice. In support of these findings, in situ hybridization showed strong expression of the ApoA-IV gene throughout the entire intestinal epithelium during developing period before weaning, but this expression was restricted to the FAE predominantly and the tips of villi to a lesser extent in adult mice. Deficiency of ApoA-IV had no effect on the organogenesis of PP in mice. Conclusions Our current results reveal ApoA-IV as a novel FAE-specific marker especially in the upper small intestine of adult mice.</description><identifier>ISSN: 0163-2116</identifier><identifier>EISSN: 1573-2568</identifier><identifier>DOI: 10.1007/s10620-014-3203-6</identifier><identifier>PMID: 24838500</identifier><identifier>CODEN: DDSCDJ</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Animals ; Antibodies, Monoclonal ; Antigens ; Apolipoproteins ; Apolipoproteins A - genetics ; Apolipoproteins A - metabolism ; Biochemistry ; Biomarkers ; CHO Cells ; Cricetinae ; Cricetulus ; Epithelium ; Female ; Gastroenterology ; Gastrointestinal system ; Gene Expression Regulation ; Hepatology ; Intestinal Mucosa - metabolism ; Intestine, Small - metabolism ; Male ; Medicine ; Medicine &amp; Public Health ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Knockout ; Monoclonal antibodies ; Oncology ; Original Article ; Peyer's Patches ; Pregnancy ; Real-Time Polymerase Chain Reaction ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger ; Transplant Surgery</subject><ispartof>Digestive diseases and sciences, 2014-11, Vol.59 (11), p.2682-2692</ispartof><rights>Springer Science+Business Media New York 2014</rights><rights>COPYRIGHT 2014 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c608t-d534e96a53edeaeac8b52e22c27ebfe329b94158c442b78b313ee19d5ae0ab393</citedby><cites>FETCH-LOGICAL-c608t-d534e96a53edeaeac8b52e22c27ebfe329b94158c442b78b313ee19d5ae0ab393</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10620-014-3203-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10620-014-3203-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24838500$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tokuhara, Daisuke</creatorcontrib><creatorcontrib>Nochi, Tomonori</creatorcontrib><creatorcontrib>Matsumura, Akiko</creatorcontrib><creatorcontrib>Mejima, Mio</creatorcontrib><creatorcontrib>Takahashi, Yuko</creatorcontrib><creatorcontrib>Kurokawa, Shiho</creatorcontrib><creatorcontrib>Kiyono, Hiroshi</creatorcontrib><creatorcontrib>Yuki, Yoshikazu</creatorcontrib><title>Specific Expression of Apolipoprotein A-IV in the Follicle-Associated Epithelium of the Small Intestine</title><title>Digestive diseases and sciences</title><addtitle>Dig Dis Sci</addtitle><addtitle>Dig Dis Sci</addtitle><description>Background Peyer’s patches (PPs), which are covered by specialized follicle-associated epithelium (FAE) including M cells, play a central role in immune induction in the gastrointestinal tract. This study is to investigate a new molecule to characterize PPs. Methods We generated a monoclonal antibody (mAb 10-15-3-3) that specifically reacts to the epithelium of PPs and isolated lymphoid follicles. Target antigen was analyzed by immunoprecipitation and mass spectrometry. Localization and expression of target antigen were evaluated by immunofluorescence, in situ hybridization and real-time PCR. Results Immunoprecipitation and mass spectrometry revealed that mAb 10-15-3-3 recognized apolipoprotein A-IV (ApoA-IV), a well-known lipid transporter; this finding was confirmed by the specific reactivity of mAb 10-15-3-3 to cells transfected with the murine ApoA-IV gene. Immunofluorescence using mAb 10-15-3-3 showed intestinal localization of ApoA-IV, in which strong expression of the ApoA-IV protein occurred throughout the entire intestinal epithelium during developing period before weaning but was restricted to the FAE in adult mice. In support of these findings, in situ hybridization showed strong expression of the ApoA-IV gene throughout the entire intestinal epithelium during developing period before weaning, but this expression was restricted to the FAE predominantly and the tips of villi to a lesser extent in adult mice. Deficiency of ApoA-IV had no effect on the organogenesis of PP in mice. 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This study is to investigate a new molecule to characterize PPs. Methods We generated a monoclonal antibody (mAb 10-15-3-3) that specifically reacts to the epithelium of PPs and isolated lymphoid follicles. Target antigen was analyzed by immunoprecipitation and mass spectrometry. Localization and expression of target antigen were evaluated by immunofluorescence, in situ hybridization and real-time PCR. Results Immunoprecipitation and mass spectrometry revealed that mAb 10-15-3-3 recognized apolipoprotein A-IV (ApoA-IV), a well-known lipid transporter; this finding was confirmed by the specific reactivity of mAb 10-15-3-3 to cells transfected with the murine ApoA-IV gene. Immunofluorescence using mAb 10-15-3-3 showed intestinal localization of ApoA-IV, in which strong expression of the ApoA-IV protein occurred throughout the entire intestinal epithelium during developing period before weaning but was restricted to the FAE in adult mice. In support of these findings, in situ hybridization showed strong expression of the ApoA-IV gene throughout the entire intestinal epithelium during developing period before weaning, but this expression was restricted to the FAE predominantly and the tips of villi to a lesser extent in adult mice. Deficiency of ApoA-IV had no effect on the organogenesis of PP in mice. Conclusions Our current results reveal ApoA-IV as a novel FAE-specific marker especially in the upper small intestine of adult mice.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>24838500</pmid><doi>10.1007/s10620-014-3203-6</doi><tpages>11</tpages></addata></record>
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subjects Animals
Antibodies, Monoclonal
Antigens
Apolipoproteins
Apolipoproteins A - genetics
Apolipoproteins A - metabolism
Biochemistry
Biomarkers
CHO Cells
Cricetinae
Cricetulus
Epithelium
Female
Gastroenterology
Gastrointestinal system
Gene Expression Regulation
Hepatology
Intestinal Mucosa - metabolism
Intestine, Small - metabolism
Male
Medicine
Medicine & Public Health
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Mice, Knockout
Monoclonal antibodies
Oncology
Original Article
Peyer's Patches
Pregnancy
Real-Time Polymerase Chain Reaction
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger
Transplant Surgery
title Specific Expression of Apolipoprotein A-IV in the Follicle-Associated Epithelium of the Small Intestine
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