Loading…
Changes in the Submandibular Salivary Gland Epithelial Cell Subpopulations During Progression of S jögren's Syndrome‐Like Disease in the NOD / S hi L t J Mouse Model
Sjögren's syndrome (SS), an autoimmune exocrinopathy, is associated with dysfunction of the secretory salivary gland epithelium, leading to xerostomia. The etiology of SS disease progression is poorly understood as it is typically not diagnosed until late stage. Since mouse models allow the stu...
Saved in:
Published in: | Anatomical record (Hoboken, N.J. : 2007) N.J. : 2007), 2015-09, Vol.298 (9), p.1622-1634 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c720-d1fbfb6f003e8c2e1f25171c4fbae81be49cfd4581c1138b4306777a5be2a0e13 |
---|---|
cites | cdi_FETCH-LOGICAL-c720-d1fbfb6f003e8c2e1f25171c4fbae81be49cfd4581c1138b4306777a5be2a0e13 |
container_end_page | 1634 |
container_issue | 9 |
container_start_page | 1622 |
container_title | Anatomical record (Hoboken, N.J. : 2007) |
container_volume | 298 |
creator | Gervais, Elise M. Desantis, Kara A. Pagendarm, Nicholas Nelson, Deirdre A. Enger, Tone Skarstein, Kathrine Liaaen Jensen, Janicke Larsen, Melinda |
description | Sjögren's syndrome (SS), an autoimmune exocrinopathy, is associated with dysfunction of the secretory salivary gland epithelium, leading to xerostomia. The etiology of SS disease progression is poorly understood as it is typically not diagnosed until late stage. Since mouse models allow the study of disease progression, we investigated the NOD/ShiLtJ mouse to explore temporal changes to the salivary epithelium. In the NOD/ShiLtJ model, SS presents secondary to autoimmune diabetes, and SS disease is reportedly fully established by 20 weeks. We compared epithelial morphology in the submandibular salivary glands (SMG) of NOD/ShiLtJ mice with SMGs from the parental strain at 12, 18, and 22 weeks of age and used immunofluorescence to detect epithelial proteins, including the acinar marker, aquaporin 5, ductal cell marker, cytokeratin 7, myoepithelial cell marker, smooth muscle α‐actin, and the basal cell marker, cytokeratin 5, while confirming immune infiltrates with CD45R. We also compared these proteins in the labial salivary glands of human SS patients with control tissues. In the NOD/ShiLtJ SMG, regions of lymphocytic infiltrates were not associated with widespread epithelial tissue degradation; however, there was a decrease in the area of the gland occupied by secretory epithelial cells in favor of ductal epithelial cells. We observed an expansion of cells expressing cytokeratin 5 within the ducts and within the smooth muscle α‐actin
+
basal myoepithelial population. The altered acinar/ductal ratio within the NOD/ShiLtJ SMG likely contributes to salivary hypofunction, while the expansion of cytokeratin 5 positive‐basal cells may reflect loss of function or indicate a regenerative response. Anat Rec, 298:1622–1634, 2015. © 2015 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/ar.23190 |
format | article |
fullrecord | <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1002_ar_23190</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1002_ar_23190</sourcerecordid><originalsourceid>FETCH-LOGICAL-c720-d1fbfb6f003e8c2e1f25171c4fbae81be49cfd4581c1138b4306777a5be2a0e13</originalsourceid><addsrcrecordid>eNo9kE1OwzAQRiMEEqUgcYTZwaatHSdNskQpFFBKkdJ9ZCfj1sWNI7tB6o4jcAxOwAW4CSch5W81ozdvZqTP884pGVJC_BG3Q5_RhBx4PZowfxAHSXD438fjY-_EuTUhYUAS1vPe0hWvl-hA1bBdIeSt2PC6UqLV3ELOtXrmdgdT3UG4blTnaMU1pKj1Xm5M05lbZWoHk9aqegmP1iwtOtcxMBJyWH-8d6C-cJDv6sqaDX6-vGbqCWGiHHKHf88f5hMYdQsrBRls4R5mpu2mM1OhPvWOJNcOz35r31vcXC_S20E2n96lV9mgjHwyqKgUUowlIQzj0kcq_ZBGtAyk4BhTgUFSyioIY1pSymIRMDKOooiHAn1OkLK-d_lztrTGOYuyaKzadBEUlBT7gAtui--A2RdHr3DV</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Changes in the Submandibular Salivary Gland Epithelial Cell Subpopulations During Progression of S jögren's Syndrome‐Like Disease in the NOD / S hi L t J Mouse Model</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Gervais, Elise M. ; Desantis, Kara A. ; Pagendarm, Nicholas ; Nelson, Deirdre A. ; Enger, Tone ; Skarstein, Kathrine ; Liaaen Jensen, Janicke ; Larsen, Melinda</creator><creatorcontrib>Gervais, Elise M. ; Desantis, Kara A. ; Pagendarm, Nicholas ; Nelson, Deirdre A. ; Enger, Tone ; Skarstein, Kathrine ; Liaaen Jensen, Janicke ; Larsen, Melinda</creatorcontrib><description>Sjögren's syndrome (SS), an autoimmune exocrinopathy, is associated with dysfunction of the secretory salivary gland epithelium, leading to xerostomia. The etiology of SS disease progression is poorly understood as it is typically not diagnosed until late stage. Since mouse models allow the study of disease progression, we investigated the NOD/ShiLtJ mouse to explore temporal changes to the salivary epithelium. In the NOD/ShiLtJ model, SS presents secondary to autoimmune diabetes, and SS disease is reportedly fully established by 20 weeks. We compared epithelial morphology in the submandibular salivary glands (SMG) of NOD/ShiLtJ mice with SMGs from the parental strain at 12, 18, and 22 weeks of age and used immunofluorescence to detect epithelial proteins, including the acinar marker, aquaporin 5, ductal cell marker, cytokeratin 7, myoepithelial cell marker, smooth muscle α‐actin, and the basal cell marker, cytokeratin 5, while confirming immune infiltrates with CD45R. We also compared these proteins in the labial salivary glands of human SS patients with control tissues. In the NOD/ShiLtJ SMG, regions of lymphocytic infiltrates were not associated with widespread epithelial tissue degradation; however, there was a decrease in the area of the gland occupied by secretory epithelial cells in favor of ductal epithelial cells. We observed an expansion of cells expressing cytokeratin 5 within the ducts and within the smooth muscle α‐actin
+
basal myoepithelial population. The altered acinar/ductal ratio within the NOD/ShiLtJ SMG likely contributes to salivary hypofunction, while the expansion of cytokeratin 5 positive‐basal cells may reflect loss of function or indicate a regenerative response. Anat Rec, 298:1622–1634, 2015. © 2015 Wiley Periodicals, Inc.</description><identifier>ISSN: 1932-8486</identifier><identifier>EISSN: 1932-8494</identifier><identifier>DOI: 10.1002/ar.23190</identifier><language>eng</language><ispartof>Anatomical record (Hoboken, N.J. : 2007), 2015-09, Vol.298 (9), p.1622-1634</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c720-d1fbfb6f003e8c2e1f25171c4fbae81be49cfd4581c1138b4306777a5be2a0e13</citedby><cites>FETCH-LOGICAL-c720-d1fbfb6f003e8c2e1f25171c4fbae81be49cfd4581c1138b4306777a5be2a0e13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Gervais, Elise M.</creatorcontrib><creatorcontrib>Desantis, Kara A.</creatorcontrib><creatorcontrib>Pagendarm, Nicholas</creatorcontrib><creatorcontrib>Nelson, Deirdre A.</creatorcontrib><creatorcontrib>Enger, Tone</creatorcontrib><creatorcontrib>Skarstein, Kathrine</creatorcontrib><creatorcontrib>Liaaen Jensen, Janicke</creatorcontrib><creatorcontrib>Larsen, Melinda</creatorcontrib><title>Changes in the Submandibular Salivary Gland Epithelial Cell Subpopulations During Progression of S jögren's Syndrome‐Like Disease in the NOD / S hi L t J Mouse Model</title><title>Anatomical record (Hoboken, N.J. : 2007)</title><description>Sjögren's syndrome (SS), an autoimmune exocrinopathy, is associated with dysfunction of the secretory salivary gland epithelium, leading to xerostomia. The etiology of SS disease progression is poorly understood as it is typically not diagnosed until late stage. Since mouse models allow the study of disease progression, we investigated the NOD/ShiLtJ mouse to explore temporal changes to the salivary epithelium. In the NOD/ShiLtJ model, SS presents secondary to autoimmune diabetes, and SS disease is reportedly fully established by 20 weeks. We compared epithelial morphology in the submandibular salivary glands (SMG) of NOD/ShiLtJ mice with SMGs from the parental strain at 12, 18, and 22 weeks of age and used immunofluorescence to detect epithelial proteins, including the acinar marker, aquaporin 5, ductal cell marker, cytokeratin 7, myoepithelial cell marker, smooth muscle α‐actin, and the basal cell marker, cytokeratin 5, while confirming immune infiltrates with CD45R. We also compared these proteins in the labial salivary glands of human SS patients with control tissues. In the NOD/ShiLtJ SMG, regions of lymphocytic infiltrates were not associated with widespread epithelial tissue degradation; however, there was a decrease in the area of the gland occupied by secretory epithelial cells in favor of ductal epithelial cells. We observed an expansion of cells expressing cytokeratin 5 within the ducts and within the smooth muscle α‐actin
+
basal myoepithelial population. The altered acinar/ductal ratio within the NOD/ShiLtJ SMG likely contributes to salivary hypofunction, while the expansion of cytokeratin 5 positive‐basal cells may reflect loss of function or indicate a regenerative response. Anat Rec, 298:1622–1634, 2015. © 2015 Wiley Periodicals, Inc.</description><issn>1932-8486</issn><issn>1932-8494</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNo9kE1OwzAQRiMEEqUgcYTZwaatHSdNskQpFFBKkdJ9ZCfj1sWNI7tB6o4jcAxOwAW4CSch5W81ozdvZqTP884pGVJC_BG3Q5_RhBx4PZowfxAHSXD438fjY-_EuTUhYUAS1vPe0hWvl-hA1bBdIeSt2PC6UqLV3ELOtXrmdgdT3UG4blTnaMU1pKj1Xm5M05lbZWoHk9aqegmP1iwtOtcxMBJyWH-8d6C-cJDv6sqaDX6-vGbqCWGiHHKHf88f5hMYdQsrBRls4R5mpu2mM1OhPvWOJNcOz35r31vcXC_S20E2n96lV9mgjHwyqKgUUowlIQzj0kcq_ZBGtAyk4BhTgUFSyioIY1pSymIRMDKOooiHAn1OkLK-d_lztrTGOYuyaKzadBEUlBT7gAtui--A2RdHr3DV</recordid><startdate>201509</startdate><enddate>201509</enddate><creator>Gervais, Elise M.</creator><creator>Desantis, Kara A.</creator><creator>Pagendarm, Nicholas</creator><creator>Nelson, Deirdre A.</creator><creator>Enger, Tone</creator><creator>Skarstein, Kathrine</creator><creator>Liaaen Jensen, Janicke</creator><creator>Larsen, Melinda</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201509</creationdate><title>Changes in the Submandibular Salivary Gland Epithelial Cell Subpopulations During Progression of S jögren's Syndrome‐Like Disease in the NOD / S hi L t J Mouse Model</title><author>Gervais, Elise M. ; Desantis, Kara A. ; Pagendarm, Nicholas ; Nelson, Deirdre A. ; Enger, Tone ; Skarstein, Kathrine ; Liaaen Jensen, Janicke ; Larsen, Melinda</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c720-d1fbfb6f003e8c2e1f25171c4fbae81be49cfd4581c1138b4306777a5be2a0e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gervais, Elise M.</creatorcontrib><creatorcontrib>Desantis, Kara A.</creatorcontrib><creatorcontrib>Pagendarm, Nicholas</creatorcontrib><creatorcontrib>Nelson, Deirdre A.</creatorcontrib><creatorcontrib>Enger, Tone</creatorcontrib><creatorcontrib>Skarstein, Kathrine</creatorcontrib><creatorcontrib>Liaaen Jensen, Janicke</creatorcontrib><creatorcontrib>Larsen, Melinda</creatorcontrib><collection>CrossRef</collection><jtitle>Anatomical record (Hoboken, N.J. : 2007)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gervais, Elise M.</au><au>Desantis, Kara A.</au><au>Pagendarm, Nicholas</au><au>Nelson, Deirdre A.</au><au>Enger, Tone</au><au>Skarstein, Kathrine</au><au>Liaaen Jensen, Janicke</au><au>Larsen, Melinda</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in the Submandibular Salivary Gland Epithelial Cell Subpopulations During Progression of S jögren's Syndrome‐Like Disease in the NOD / S hi L t J Mouse Model</atitle><jtitle>Anatomical record (Hoboken, N.J. : 2007)</jtitle><date>2015-09</date><risdate>2015</risdate><volume>298</volume><issue>9</issue><spage>1622</spage><epage>1634</epage><pages>1622-1634</pages><issn>1932-8486</issn><eissn>1932-8494</eissn><abstract>Sjögren's syndrome (SS), an autoimmune exocrinopathy, is associated with dysfunction of the secretory salivary gland epithelium, leading to xerostomia. The etiology of SS disease progression is poorly understood as it is typically not diagnosed until late stage. Since mouse models allow the study of disease progression, we investigated the NOD/ShiLtJ mouse to explore temporal changes to the salivary epithelium. In the NOD/ShiLtJ model, SS presents secondary to autoimmune diabetes, and SS disease is reportedly fully established by 20 weeks. We compared epithelial morphology in the submandibular salivary glands (SMG) of NOD/ShiLtJ mice with SMGs from the parental strain at 12, 18, and 22 weeks of age and used immunofluorescence to detect epithelial proteins, including the acinar marker, aquaporin 5, ductal cell marker, cytokeratin 7, myoepithelial cell marker, smooth muscle α‐actin, and the basal cell marker, cytokeratin 5, while confirming immune infiltrates with CD45R. We also compared these proteins in the labial salivary glands of human SS patients with control tissues. In the NOD/ShiLtJ SMG, regions of lymphocytic infiltrates were not associated with widespread epithelial tissue degradation; however, there was a decrease in the area of the gland occupied by secretory epithelial cells in favor of ductal epithelial cells. We observed an expansion of cells expressing cytokeratin 5 within the ducts and within the smooth muscle α‐actin
+
basal myoepithelial population. The altered acinar/ductal ratio within the NOD/ShiLtJ SMG likely contributes to salivary hypofunction, while the expansion of cytokeratin 5 positive‐basal cells may reflect loss of function or indicate a regenerative response. Anat Rec, 298:1622–1634, 2015. © 2015 Wiley Periodicals, Inc.</abstract><doi>10.1002/ar.23190</doi><tpages>13</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-8486 |
ispartof | Anatomical record (Hoboken, N.J. : 2007), 2015-09, Vol.298 (9), p.1622-1634 |
issn | 1932-8486 1932-8494 |
language | eng |
recordid | cdi_crossref_primary_10_1002_ar_23190 |
source | Wiley-Blackwell Read & Publish Collection |
title | Changes in the Submandibular Salivary Gland Epithelial Cell Subpopulations During Progression of S jögren's Syndrome‐Like Disease in the NOD / S hi L t J Mouse Model |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T20%3A01%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Changes%20in%20the%20Submandibular%20Salivary%20Gland%20Epithelial%20Cell%20Subpopulations%20During%20Progression%20of%20S%20j%C3%B6gren's%20Syndrome%E2%80%90Like%20Disease%20in%20the%20NOD%20/%20S%20hi%20L%20t%20J%20Mouse%20Model&rft.jtitle=Anatomical%20record%20(Hoboken,%20N.J.%20:%202007)&rft.au=Gervais,%20Elise%20M.&rft.date=2015-09&rft.volume=298&rft.issue=9&rft.spage=1622&rft.epage=1634&rft.pages=1622-1634&rft.issn=1932-8486&rft.eissn=1932-8494&rft_id=info:doi/10.1002/ar.23190&rft_dat=%3Ccrossref%3E10_1002_ar_23190%3C/crossref%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c720-d1fbfb6f003e8c2e1f25171c4fbae81be49cfd4581c1138b4306777a5be2a0e13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |