Intestinal Epithelial Cell Brush Border Membrane Cl:HCO[sub.3] Exchanger Regulation by Mast Cells in Chronic Ileitis
Malabsorption of NaCl is the primary cause of diarrhea in inflammatory bowel disease (IBD). Coupled NaCl absorption occurs via the dual operation of Na:H and Cl:HCO[sub.3] exchange in the brush border membrane (BBM) of villus cells. Cl:HCO[sub.3] exchange is mediated by BBM transporters DRA (downreg...
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description | Malabsorption of NaCl is the primary cause of diarrhea in inflammatory bowel disease (IBD). Coupled NaCl absorption occurs via the dual operation of Na:H and Cl:HCO[sub.3] exchange in the brush border membrane (BBM) of villus cells. Cl:HCO[sub.3] exchange is mediated by BBM transporters DRA (downregulated in adenoma) and PAT1 (putative anion transporter 1) in the mammalian small intestine. DRA/PAT1-mediated Cl:HCO[sub.3] exchange was significantly downregulated in the BBM of villus cells in a rabbit model of chronic ileitis, while Na:H exchange was unaffected. The inhibition of Cl:HCO[sub.3] exchange was restored in the rabbits when treated with a broad-spectrum immunomodulator, i.e. a glucocorticoid, indicating that the downregulation of DRA/PAT1 is likely to be immune-mediated during chronic enteritis. Mucosal mast cells are one type of key immune cells that are known to proliferate and release immune inflammatory mediators, thus playing a significant role in the pathogenesis of IBD. However, how mast cells may regulate DRA- and PAT1-mediated Cl:HCO[sub.3] exchange in a rabbit model of chronic ileitis is unknown. In this study, treatment of rabbits with chronic intestinal inflammation with the mast cell stabilizer ketotifen did not affect the mucosal architecture of the inflamed intestine. However, ketotifen treatment reversed the inhibition of Cl:HCO[sub.3] activity in the BBM of villus cells. This restoration of Cl:HCO[sub.3] activity to normal levels by ketotifen was found to be secondary to restoring the affinity of the exchangers for its substrate chloride. This observation was consistent with molecular studies, where the mRNA and BBM protein expressions of DRA and PAT1 remained unaffected in the villus cells under all experimental conditions. Thus, this study indicates that mast cells mediated the inhibition of coupled NaCl absorption by inhibiting Cl:HCO[sub.3] exchange in a rabbit model of chronic enteritis. |
doi_str_mv | 10.3390/ijms252011208 |
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Coupled NaCl absorption occurs via the dual operation of Na:H and Cl:HCO[sub.3] exchange in the brush border membrane (BBM) of villus cells. Cl:HCO[sub.3] exchange is mediated by BBM transporters DRA (downregulated in adenoma) and PAT1 (putative anion transporter 1) in the mammalian small intestine. DRA/PAT1-mediated Cl:HCO[sub.3] exchange was significantly downregulated in the BBM of villus cells in a rabbit model of chronic ileitis, while Na:H exchange was unaffected. The inhibition of Cl:HCO[sub.3] exchange was restored in the rabbits when treated with a broad-spectrum immunomodulator, i.e. a glucocorticoid, indicating that the downregulation of DRA/PAT1 is likely to be immune-mediated during chronic enteritis. Mucosal mast cells are one type of key immune cells that are known to proliferate and release immune inflammatory mediators, thus playing a significant role in the pathogenesis of IBD. However, how mast cells may regulate DRA- and PAT1-mediated Cl:HCO[sub.3] exchange in a rabbit model of chronic ileitis is unknown. In this study, treatment of rabbits with chronic intestinal inflammation with the mast cell stabilizer ketotifen did not affect the mucosal architecture of the inflamed intestine. However, ketotifen treatment reversed the inhibition of Cl:HCO[sub.3] activity in the BBM of villus cells. This restoration of Cl:HCO[sub.3] activity to normal levels by ketotifen was found to be secondary to restoring the affinity of the exchangers for its substrate chloride. This observation was consistent with molecular studies, where the mRNA and BBM protein expressions of DRA and PAT1 remained unaffected in the villus cells under all experimental conditions. Thus, this study indicates that mast cells mediated the inhibition of coupled NaCl absorption by inhibiting Cl:HCO[sub.3] exchange in a rabbit model of chronic enteritis.</description><identifier>ISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms252011208</identifier><language>eng</language><publisher>MDPI AG</publisher><subject>Analysis ; Care and treatment ; Diagnosis ; Dosage and administration ; Immune response ; Immunity ; Inflammatory bowel diseases ; Malnutrition ; Prevention ; Risk factors</subject><ispartof>International journal of molecular sciences, 2024-10, Vol.25 (20)</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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>Paulraj, Raja Singh</creatorcontrib><creatorcontrib>Afroz, Sheuli</creatorcontrib><creatorcontrib>Palaniappan, Balasubramanian</creatorcontrib><creatorcontrib>Murughiyan, Usha</creatorcontrib><creatorcontrib>Singh, Soudamani</creatorcontrib><creatorcontrib>Arthur, Subha</creatorcontrib><creatorcontrib>Sundaram, Uma</creatorcontrib><title>Intestinal Epithelial Cell Brush Border Membrane Cl:HCO[sub.3] Exchanger Regulation by Mast Cells in Chronic Ileitis</title><title>International journal of molecular sciences</title><description>Malabsorption of NaCl is the primary cause of diarrhea in inflammatory bowel disease (IBD). Coupled NaCl absorption occurs via the dual operation of Na:H and Cl:HCO[sub.3] exchange in the brush border membrane (BBM) of villus cells. Cl:HCO[sub.3] exchange is mediated by BBM transporters DRA (downregulated in adenoma) and PAT1 (putative anion transporter 1) in the mammalian small intestine. DRA/PAT1-mediated Cl:HCO[sub.3] exchange was significantly downregulated in the BBM of villus cells in a rabbit model of chronic ileitis, while Na:H exchange was unaffected. The inhibition of Cl:HCO[sub.3] exchange was restored in the rabbits when treated with a broad-spectrum immunomodulator, i.e. a glucocorticoid, indicating that the downregulation of DRA/PAT1 is likely to be immune-mediated during chronic enteritis. Mucosal mast cells are one type of key immune cells that are known to proliferate and release immune inflammatory mediators, thus playing a significant role in the pathogenesis of IBD. However, how mast cells may regulate DRA- and PAT1-mediated Cl:HCO[sub.3] exchange in a rabbit model of chronic ileitis is unknown. In this study, treatment of rabbits with chronic intestinal inflammation with the mast cell stabilizer ketotifen did not affect the mucosal architecture of the inflamed intestine. However, ketotifen treatment reversed the inhibition of Cl:HCO[sub.3] activity in the BBM of villus cells. This restoration of Cl:HCO[sub.3] activity to normal levels by ketotifen was found to be secondary to restoring the affinity of the exchangers for its substrate chloride. This observation was consistent with molecular studies, where the mRNA and BBM protein expressions of DRA and PAT1 remained unaffected in the villus cells under all experimental conditions. Thus, this study indicates that mast cells mediated the inhibition of coupled NaCl absorption by inhibiting Cl:HCO[sub.3] exchange in a rabbit model of chronic enteritis.</description><subject>Analysis</subject><subject>Care and treatment</subject><subject>Diagnosis</subject><subject>Dosage and administration</subject><subject>Immune response</subject><subject>Immunity</subject><subject>Inflammatory bowel diseases</subject><subject>Malnutrition</subject><subject>Prevention</subject><subject>Risk factors</subject><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptj89LwzAUx3NQcE6P3gOeO_Oj7RJvW5lusDGQ3URGkr60GWkqTQb631vUgwd5h-_jy-d94CF0R8mMc0ke3KmLrGCEUkbEBZrQnLGMkHJ-ha5jPBHCOCvkBKVNSBCTC8rj1btLLXg3rhV4j5fDObZ42Q81DHgHnR5UAFz5x3W1f41nPeNvePVhWhWaEXiB5uxVcn3A-hPvVEzflohdwFU79MEZvPHgkos36NIqH-H2N6fo8LQ6VOtsu3_eVItt1pRzntWEKEFrqgWwnEqAolQw_pML0LWhMhfW1IXRmhZQM0uJkbQkTBsruJVG8im6_9E2ysPRBdunQZnORXNcCJpzyYs5H6nZP9Q4NXTO9AGsG_s_B183O2r0</recordid><startdate>20241001</startdate><enddate>20241001</enddate><creator>Paulraj, Raja Singh</creator><creator>Afroz, Sheuli</creator><creator>Palaniappan, Balasubramanian</creator><creator>Murughiyan, Usha</creator><creator>Singh, Soudamani</creator><creator>Arthur, Subha</creator><creator>Sundaram, Uma</creator><general>MDPI AG</general><scope/></search><sort><creationdate>20241001</creationdate><title>Intestinal Epithelial Cell Brush Border Membrane Cl:HCO[sub.3] Exchanger Regulation by Mast Cells in Chronic Ileitis</title><author>Paulraj, Raja Singh ; Afroz, Sheuli ; Palaniappan, Balasubramanian ; Murughiyan, Usha ; Singh, Soudamani ; Arthur, Subha ; Sundaram, Uma</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g673-d00a81d1b8e2419ee56ae11248ebdc1948fcd5cbb15ed2f10c91602bcf83f9c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Analysis</topic><topic>Care and treatment</topic><topic>Diagnosis</topic><topic>Dosage and administration</topic><topic>Immune response</topic><topic>Immunity</topic><topic>Inflammatory bowel diseases</topic><topic>Malnutrition</topic><topic>Prevention</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Paulraj, Raja Singh</creatorcontrib><creatorcontrib>Afroz, Sheuli</creatorcontrib><creatorcontrib>Palaniappan, Balasubramanian</creatorcontrib><creatorcontrib>Murughiyan, Usha</creatorcontrib><creatorcontrib>Singh, Soudamani</creatorcontrib><creatorcontrib>Arthur, Subha</creatorcontrib><creatorcontrib>Sundaram, Uma</creatorcontrib><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Paulraj, Raja Singh</au><au>Afroz, Sheuli</au><au>Palaniappan, Balasubramanian</au><au>Murughiyan, Usha</au><au>Singh, Soudamani</au><au>Arthur, Subha</au><au>Sundaram, Uma</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intestinal Epithelial Cell Brush Border Membrane Cl:HCO[sub.3] Exchanger Regulation by Mast Cells in Chronic Ileitis</atitle><jtitle>International journal of molecular sciences</jtitle><date>2024-10-01</date><risdate>2024</risdate><volume>25</volume><issue>20</issue><issn>1422-0067</issn><abstract>Malabsorption of NaCl is the primary cause of diarrhea in inflammatory bowel disease (IBD). Coupled NaCl absorption occurs via the dual operation of Na:H and Cl:HCO[sub.3] exchange in the brush border membrane (BBM) of villus cells. Cl:HCO[sub.3] exchange is mediated by BBM transporters DRA (downregulated in adenoma) and PAT1 (putative anion transporter 1) in the mammalian small intestine. DRA/PAT1-mediated Cl:HCO[sub.3] exchange was significantly downregulated in the BBM of villus cells in a rabbit model of chronic ileitis, while Na:H exchange was unaffected. The inhibition of Cl:HCO[sub.3] exchange was restored in the rabbits when treated with a broad-spectrum immunomodulator, i.e. a glucocorticoid, indicating that the downregulation of DRA/PAT1 is likely to be immune-mediated during chronic enteritis. Mucosal mast cells are one type of key immune cells that are known to proliferate and release immune inflammatory mediators, thus playing a significant role in the pathogenesis of IBD. However, how mast cells may regulate DRA- and PAT1-mediated Cl:HCO[sub.3] exchange in a rabbit model of chronic ileitis is unknown. In this study, treatment of rabbits with chronic intestinal inflammation with the mast cell stabilizer ketotifen did not affect the mucosal architecture of the inflamed intestine. However, ketotifen treatment reversed the inhibition of Cl:HCO[sub.3] activity in the BBM of villus cells. This restoration of Cl:HCO[sub.3] activity to normal levels by ketotifen was found to be secondary to restoring the affinity of the exchangers for its substrate chloride. This observation was consistent with molecular studies, where the mRNA and BBM protein expressions of DRA and PAT1 remained unaffected in the villus cells under all experimental conditions. Thus, this study indicates that mast cells mediated the inhibition of coupled NaCl absorption by inhibiting Cl:HCO[sub.3] exchange in a rabbit model of chronic enteritis.</abstract><pub>MDPI AG</pub><doi>10.3390/ijms252011208</doi></addata></record> |
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subjects | Analysis Care and treatment Diagnosis Dosage and administration Immune response Immunity Inflammatory bowel diseases Malnutrition Prevention Risk factors |
title | Intestinal Epithelial Cell Brush Border Membrane Cl:HCO[sub.3] Exchanger Regulation by Mast Cells in Chronic Ileitis |
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