Neutrophil migration in mice induced by a mannose-binding lectin isolated from Annona coriacea seeds
A novel 14-kDa lectin from Annona coriacea seeds (ACLEC) with hemagglutinating activity on erythrocytes has been recently described. Since plant lectins are known to present inflammatory activity, this study aimed to investigate the leukocyte migration induced by ACLEC, and inflammatory mediators in...
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description | A novel 14-kDa lectin from
Annona coriacea seeds (ACLEC) with hemagglutinating activity on erythrocytes has been recently described. Since plant lectins are known to present inflammatory activity, this study aimed to investigate the leukocyte migration induced by ACLEC, and inflammatory mediators involved in this phenomenon. Male Swiss mice were intraperitoneally injected with ACLEC (3–100
μg/cavity), and at 4–96
h thereafter the leukocyte counts in peritoneal lavage fluid were evaluated. ACLEC induced a dose-dependent neutrophil accumulation, reaching maximal responses at 16
h after injection (approximately 40-fold increase for 30
μg/cavity). Significant accumulation of mononuclear cells was observed at 72
h (2.7-fold increase). The carbohydrate mannose nearly abolished the neutrophil influx, whereas sucrose, glucose and galactose had no effect. Dexamethasone, the cyclooxygenase-2 (COX-2) inhibitor celecoxib and the Platelet activating factor (PAF) receptor antagonist PCA4248 significantly reduced ACLEC-induced neutrophil influx. The tachykinin NK
1 antagonist SR140333, the tachykinin NK
2 antagonist SR48968, the non-selective NO inhibitor L-NAME, the selective inducible NOS inhibitor aminoguanidine and the lypoxygenase inhibitor AA861 all failed to modify the ACLEC-induced responses. In conclusion, ACLEC is able to attract neutrophils into the mice peritoneal cavity by mechanisms involving interactions of the lectin with cell-specific mannose recognition, leading to the release of COX-2-derived mediators and PAF. |
doi_str_mv | 10.1016/j.toxicon.2006.07.001 |
format | Article |
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Annona coriacea seeds (ACLEC) with hemagglutinating activity on erythrocytes has been recently described. Since plant lectins are known to present inflammatory activity, this study aimed to investigate the leukocyte migration induced by ACLEC, and inflammatory mediators involved in this phenomenon. Male Swiss mice were intraperitoneally injected with ACLEC (3–100
μg/cavity), and at 4–96
h thereafter the leukocyte counts in peritoneal lavage fluid were evaluated. ACLEC induced a dose-dependent neutrophil accumulation, reaching maximal responses at 16
h after injection (approximately 40-fold increase for 30
μg/cavity). Significant accumulation of mononuclear cells was observed at 72
h (2.7-fold increase). The carbohydrate mannose nearly abolished the neutrophil influx, whereas sucrose, glucose and galactose had no effect. Dexamethasone, the cyclooxygenase-2 (COX-2) inhibitor celecoxib and the Platelet activating factor (PAF) receptor antagonist PCA4248 significantly reduced ACLEC-induced neutrophil influx. The tachykinin NK
1 antagonist SR140333, the tachykinin NK
2 antagonist SR48968, the non-selective NO inhibitor L-NAME, the selective inducible NOS inhibitor aminoguanidine and the lypoxygenase inhibitor AA861 all failed to modify the ACLEC-induced responses. In conclusion, ACLEC is able to attract neutrophils into the mice peritoneal cavity by mechanisms involving interactions of the lectin with cell-specific mannose recognition, leading to the release of COX-2-derived mediators and PAF.</description><identifier>ISSN: 0041-0101</identifier><identifier>EISSN: 1879-3150</identifier><identifier>DOI: 10.1016/j.toxicon.2006.07.001</identifier><identifier>PMID: 16926040</identifier><identifier>CODEN: TOXIA6</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; Annona - chemistry ; Annona coriacea ; Annona coriacea lectin ; Biological and medical sciences ; Celecoxib ; Chemotaxis, Leukocyte - drug effects ; Chemotaxis, Leukocyte - immunology ; Dihydropyridines - pharmacology ; Dose-Response Relationship, Drug ; Inflammation ; Leukocytes, Mononuclear - drug effects ; Leukocytes, Mononuclear - immunology ; Leukocytes, Mononuclear - pathology ; Male ; Mannose - pharmacology ; Mannose-Binding Lectin - immunology ; Mannose-Binding Lectin - toxicity ; Medical sciences ; Mice ; Neutrophil migration ; Neutrophils - drug effects ; Neutrophils - immunology ; Neutrophils - pathology ; Peritoneal Cavity ; Plant Extracts - immunology ; Plant Extracts - toxicity ; Plant poisons toxicology ; Pyrazoles - pharmacology ; Seeds - chemistry ; Sulfonamides - pharmacology ; Toxicology</subject><ispartof>Toxicon (Oxford), 2006-10, Vol.48 (5), p.529-535</ispartof><rights>2006 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-fee4a1ecf06363057f9f60b4e78c6d8938b489176828251334e889ef4d9cc7133</citedby><cites>FETCH-LOGICAL-c424t-fee4a1ecf06363057f9f60b4e78c6d8938b489176828251334e889ef4d9cc7133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.toxicon.2006.07.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3552,27931,27932,46002</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18109863$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16926040$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Coelho, Mirela B.</creatorcontrib><creatorcontrib>DeSouza, Ivani A.</creatorcontrib><creatorcontrib>Freire, Maria Graça M.</creatorcontrib><creatorcontrib>Marangoni, Sérgio</creatorcontrib><creatorcontrib>Antunes, Edson</creatorcontrib><creatorcontrib>Macedo, Maria Lígia R.</creatorcontrib><title>Neutrophil migration in mice induced by a mannose-binding lectin isolated from Annona coriacea seeds</title><title>Toxicon (Oxford)</title><addtitle>Toxicon</addtitle><description>A novel 14-kDa lectin from
Annona coriacea seeds (ACLEC) with hemagglutinating activity on erythrocytes has been recently described. Since plant lectins are known to present inflammatory activity, this study aimed to investigate the leukocyte migration induced by ACLEC, and inflammatory mediators involved in this phenomenon. Male Swiss mice were intraperitoneally injected with ACLEC (3–100
μg/cavity), and at 4–96
h thereafter the leukocyte counts in peritoneal lavage fluid were evaluated. ACLEC induced a dose-dependent neutrophil accumulation, reaching maximal responses at 16
h after injection (approximately 40-fold increase for 30
μg/cavity). Significant accumulation of mononuclear cells was observed at 72
h (2.7-fold increase). The carbohydrate mannose nearly abolished the neutrophil influx, whereas sucrose, glucose and galactose had no effect. Dexamethasone, the cyclooxygenase-2 (COX-2) inhibitor celecoxib and the Platelet activating factor (PAF) receptor antagonist PCA4248 significantly reduced ACLEC-induced neutrophil influx. The tachykinin NK
1 antagonist SR140333, the tachykinin NK
2 antagonist SR48968, the non-selective NO inhibitor L-NAME, the selective inducible NOS inhibitor aminoguanidine and the lypoxygenase inhibitor AA861 all failed to modify the ACLEC-induced responses. In conclusion, ACLEC is able to attract neutrophils into the mice peritoneal cavity by mechanisms involving interactions of the lectin with cell-specific mannose recognition, leading to the release of COX-2-derived mediators and PAF.</description><subject>Animals</subject><subject>Annona - chemistry</subject><subject>Annona coriacea</subject><subject>Annona coriacea lectin</subject><subject>Biological and medical sciences</subject><subject>Celecoxib</subject><subject>Chemotaxis, Leukocyte - drug effects</subject><subject>Chemotaxis, Leukocyte - immunology</subject><subject>Dihydropyridines - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Inflammation</subject><subject>Leukocytes, Mononuclear - drug effects</subject><subject>Leukocytes, Mononuclear - immunology</subject><subject>Leukocytes, Mononuclear - pathology</subject><subject>Male</subject><subject>Mannose - pharmacology</subject><subject>Mannose-Binding Lectin - immunology</subject><subject>Mannose-Binding Lectin - toxicity</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Neutrophil migration</subject><subject>Neutrophils - drug effects</subject><subject>Neutrophils - immunology</subject><subject>Neutrophils - pathology</subject><subject>Peritoneal Cavity</subject><subject>Plant Extracts - immunology</subject><subject>Plant Extracts - toxicity</subject><subject>Plant poisons toxicology</subject><subject>Pyrazoles - pharmacology</subject><subject>Seeds - chemistry</subject><subject>Sulfonamides - pharmacology</subject><subject>Toxicology</subject><issn>0041-0101</issn><issn>1879-3150</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMFu1DAQhi1ERZfCI4B8obek49jr2CdUVRSQKrjA2XKccfEqsRc7QfTt8Woj9chpNKNvZn59hLxj0DJg8ubQLulvcCm2HYBsoW8B2AuyY6rXDWd7eEl2AII1UPFL8rqUAwBwpeUrcsmk7iQI2JHxG65LTsdfYaJzeMx2CSnSEGvjsNZxdTjS4YlaOtsYU8FmqNMQH-mEbqlgKGmyS4V8TjO9rUy01KUcrENLC-JY3pALb6eCb7d6RX7ef_px96V5-P75693tQ-NEJ5bGIwrL0HmQXHLY9157CYPAXjk5Ks3VIJRmvVSd6vaMc4FKafRi1M71tb8i1-e7x5x-r1gWM4ficJpsxLQWwzTnUkpWwf0ZdDmVktGbYw6zzU-GgTnpNQez6TUnvQZ6U_XWvffbg3WYcXze2nxW4MMG2OLs5LONLpRnTjHQSp6SfjxzWHX8CZhNcQFjdR1y1WrGFP4T5R-ew5u_</recordid><startdate>20061001</startdate><enddate>20061001</enddate><creator>Coelho, Mirela B.</creator><creator>DeSouza, Ivani A.</creator><creator>Freire, Maria Graça M.</creator><creator>Marangoni, Sérgio</creator><creator>Antunes, Edson</creator><creator>Macedo, Maria Lígia R.</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20061001</creationdate><title>Neutrophil migration in mice induced by a mannose-binding lectin isolated from Annona coriacea seeds</title><author>Coelho, Mirela B. ; DeSouza, Ivani A. ; Freire, Maria Graça M. ; Marangoni, Sérgio ; Antunes, Edson ; Macedo, Maria Lígia R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-fee4a1ecf06363057f9f60b4e78c6d8938b489176828251334e889ef4d9cc7133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Annona - chemistry</topic><topic>Annona coriacea</topic><topic>Annona coriacea lectin</topic><topic>Biological and medical sciences</topic><topic>Celecoxib</topic><topic>Chemotaxis, Leukocyte - drug effects</topic><topic>Chemotaxis, Leukocyte - immunology</topic><topic>Dihydropyridines - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Inflammation</topic><topic>Leukocytes, Mononuclear - drug effects</topic><topic>Leukocytes, Mononuclear - immunology</topic><topic>Leukocytes, Mononuclear - pathology</topic><topic>Male</topic><topic>Mannose - pharmacology</topic><topic>Mannose-Binding Lectin - immunology</topic><topic>Mannose-Binding Lectin - toxicity</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Neutrophil migration</topic><topic>Neutrophils - drug effects</topic><topic>Neutrophils - immunology</topic><topic>Neutrophils - pathology</topic><topic>Peritoneal Cavity</topic><topic>Plant Extracts - immunology</topic><topic>Plant Extracts - toxicity</topic><topic>Plant poisons toxicology</topic><topic>Pyrazoles - pharmacology</topic><topic>Seeds - chemistry</topic><topic>Sulfonamides - pharmacology</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Coelho, Mirela B.</creatorcontrib><creatorcontrib>DeSouza, Ivani A.</creatorcontrib><creatorcontrib>Freire, Maria Graça M.</creatorcontrib><creatorcontrib>Marangoni, Sérgio</creatorcontrib><creatorcontrib>Antunes, Edson</creatorcontrib><creatorcontrib>Macedo, Maria Lígia R.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicon (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Coelho, Mirela B.</au><au>DeSouza, Ivani A.</au><au>Freire, Maria Graça M.</au><au>Marangoni, Sérgio</au><au>Antunes, Edson</au><au>Macedo, Maria Lígia R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neutrophil migration in mice induced by a mannose-binding lectin isolated from Annona coriacea seeds</atitle><jtitle>Toxicon (Oxford)</jtitle><addtitle>Toxicon</addtitle><date>2006-10-01</date><risdate>2006</risdate><volume>48</volume><issue>5</issue><spage>529</spage><epage>535</epage><pages>529-535</pages><issn>0041-0101</issn><eissn>1879-3150</eissn><coden>TOXIA6</coden><abstract>A novel 14-kDa lectin from
Annona coriacea seeds (ACLEC) with hemagglutinating activity on erythrocytes has been recently described. Since plant lectins are known to present inflammatory activity, this study aimed to investigate the leukocyte migration induced by ACLEC, and inflammatory mediators involved in this phenomenon. Male Swiss mice were intraperitoneally injected with ACLEC (3–100
μg/cavity), and at 4–96
h thereafter the leukocyte counts in peritoneal lavage fluid were evaluated. ACLEC induced a dose-dependent neutrophil accumulation, reaching maximal responses at 16
h after injection (approximately 40-fold increase for 30
μg/cavity). Significant accumulation of mononuclear cells was observed at 72
h (2.7-fold increase). The carbohydrate mannose nearly abolished the neutrophil influx, whereas sucrose, glucose and galactose had no effect. Dexamethasone, the cyclooxygenase-2 (COX-2) inhibitor celecoxib and the Platelet activating factor (PAF) receptor antagonist PCA4248 significantly reduced ACLEC-induced neutrophil influx. The tachykinin NK
1 antagonist SR140333, the tachykinin NK
2 antagonist SR48968, the non-selective NO inhibitor L-NAME, the selective inducible NOS inhibitor aminoguanidine and the lypoxygenase inhibitor AA861 all failed to modify the ACLEC-induced responses. In conclusion, ACLEC is able to attract neutrophils into the mice peritoneal cavity by mechanisms involving interactions of the lectin with cell-specific mannose recognition, leading to the release of COX-2-derived mediators and PAF.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>16926040</pmid><doi>10.1016/j.toxicon.2006.07.001</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Annona - chemistry Annona coriacea Annona coriacea lectin Biological and medical sciences Celecoxib Chemotaxis, Leukocyte - drug effects Chemotaxis, Leukocyte - immunology Dihydropyridines - pharmacology Dose-Response Relationship, Drug Inflammation Leukocytes, Mononuclear - drug effects Leukocytes, Mononuclear - immunology Leukocytes, Mononuclear - pathology Male Mannose - pharmacology Mannose-Binding Lectin - immunology Mannose-Binding Lectin - toxicity Medical sciences Mice Neutrophil migration Neutrophils - drug effects Neutrophils - immunology Neutrophils - pathology Peritoneal Cavity Plant Extracts - immunology Plant Extracts - toxicity Plant poisons toxicology Pyrazoles - pharmacology Seeds - chemistry Sulfonamides - pharmacology Toxicology |
title | Neutrophil migration in mice induced by a mannose-binding lectin isolated from Annona coriacea seeds |
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