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Site-specific Differences in Gene Expression of Secreted Proteins in the Mouse Lung: Comparison of Methods to Show Differences by Location
Studies on the effects of pulmonary toxicants on the lung often overlook the fact that site-specific changes are likely to occur in response to chemical exposure. These changes can be highly focal and may be undetected by methods that do not examine specific lung regions. This problem is especially...
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Published in: | The journal of histochemistry and cytochemistry 2010-12, Vol.58 (12), p.1107-1119 |
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description | Studies on the effects of pulmonary toxicants on the lung often overlook the fact that site-specific changes are likely to occur in response to chemical exposure. These changes can be highly focal and may be undetected by methods that do not examine specific lung regions. This problem is especially acute for studies of the conducting airways. In this study, differential gene expression of secreted proteins in the lung by different methods of collection (whole lung, gross airway microdissection, and laser capture microdissection) and by airway levels (whole lobe, whole airway tree, proximal airways, airway bifurcations, and terminal bronchioles) was examined. Site-specific sampling approaches were combined with methods to detect both gene and corresponding protein expression in different lung regions. Differential expression of mRNA by both airway level and lung region was determined for Clara cell secretory protein, calcitonin gene-related peptide, uteroglobin-related protein 2, surfactant protein A, and surfactant protein C. Therefore, for maximal enrichment of mRNA and maximal ability to identify changes in mRNA levels in the diseased state or in response to chemical exposure, it is critical to choose the appropriate airway region and sample collection method to enrich detection of the transcript(s) of interest. (J Histochem Cytochem 58:1107–1119, 2010) |
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Differential expression of mRNA by both airway level and lung region was determined for Clara cell secretory protein, calcitonin gene-related peptide, uteroglobin-related protein 2, surfactant protein A, and surfactant protein C. Therefore, for maximal enrichment of mRNA and maximal ability to identify changes in mRNA levels in the diseased state or in response to chemical exposure, it is critical to choose the appropriate airway region and sample collection method to enrich detection of the transcript(s) of interest. 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Van Winkle</creatorcontrib><title>Site-specific Differences in Gene Expression of Secreted Proteins in the Mouse Lung: Comparison of Methods to Show Differences by Location</title><title>The journal of histochemistry and cytochemistry</title><addtitle>J Histochem Cytochem</addtitle><description>Studies on the effects of pulmonary toxicants on the lung often overlook the fact that site-specific changes are likely to occur in response to chemical exposure. These changes can be highly focal and may be undetected by methods that do not examine specific lung regions. This problem is especially acute for studies of the conducting airways. In this study, differential gene expression of secreted proteins in the lung by different methods of collection (whole lung, gross airway microdissection, and laser capture microdissection) and by airway levels (whole lobe, whole airway tree, proximal airways, airway bifurcations, and terminal bronchioles) was examined. Site-specific sampling approaches were combined with methods to detect both gene and corresponding protein expression in different lung regions. Differential expression of mRNA by both airway level and lung region was determined for Clara cell secretory protein, calcitonin gene-related peptide, uteroglobin-related protein 2, surfactant protein A, and surfactant protein C. Therefore, for maximal enrichment of mRNA and maximal ability to identify changes in mRNA levels in the diseased state or in response to chemical exposure, it is critical to choose the appropriate airway region and sample collection method to enrich detection of the transcript(s) of interest. 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Van Winkle</creator><general>SAGE Publications</general><general>Histochemical Society</general><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>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20101201</creationdate><title>Site-specific Differences in Gene Expression of Secreted Proteins in the Mouse Lung: Comparison of Methods to Show Differences by Location</title><author>Sutherland, Katherine M. ; Combs, Trenton J. ; Edwards, Patricia C. ; Laura, S. Van Winkle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c527t-32895513b2dd4e8f61aff876b312cf20f25a0e72e0bccaba30431698d520b2b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Calcitonin Gene-Related Peptide - biosynthesis</topic><topic>Calcitonin Gene-Related Peptide - genetics</topic><topic>Calcitonin Gene-Related Peptide - secretion</topic><topic>Gene Expression Profiling</topic><topic>Immunohistochemistry</topic><topic>Lung - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Organ Specificity</topic><topic>Proteins - genetics</topic><topic>Proteins - metabolism</topic><topic>Proteins - secretion</topic><topic>Pulmonary Surfactant-Associated Protein A - biosynthesis</topic><topic>Pulmonary Surfactant-Associated Protein A - genetics</topic><topic>Pulmonary Surfactant-Associated Protein A - secretion</topic><topic>Pulmonary Surfactant-Associated Protein C - biosynthesis</topic><topic>Pulmonary Surfactant-Associated Protein C - genetics</topic><topic>Pulmonary Surfactant-Associated Protein C - secretion</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - biosynthesis</topic><topic>RNA, Messenger - genetics</topic><topic>Uteroglobin - biosynthesis</topic><topic>Uteroglobin - genetics</topic><topic>Uteroglobin - secretion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sutherland, Katherine M.</creatorcontrib><creatorcontrib>Combs, Trenton J.</creatorcontrib><creatorcontrib>Edwards, Patricia C.</creatorcontrib><creatorcontrib>Laura, S. 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Van Winkle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Site-specific Differences in Gene Expression of Secreted Proteins in the Mouse Lung: Comparison of Methods to Show Differences by Location</atitle><jtitle>The journal of histochemistry and cytochemistry</jtitle><addtitle>J Histochem Cytochem</addtitle><date>2010-12-01</date><risdate>2010</risdate><volume>58</volume><issue>12</issue><spage>1107</spage><epage>1119</epage><pages>1107-1119</pages><issn>0022-1554</issn><eissn>1551-5044</eissn><abstract>Studies on the effects of pulmonary toxicants on the lung often overlook the fact that site-specific changes are likely to occur in response to chemical exposure. These changes can be highly focal and may be undetected by methods that do not examine specific lung regions. This problem is especially acute for studies of the conducting airways. In this study, differential gene expression of secreted proteins in the lung by different methods of collection (whole lung, gross airway microdissection, and laser capture microdissection) and by airway levels (whole lobe, whole airway tree, proximal airways, airway bifurcations, and terminal bronchioles) was examined. Site-specific sampling approaches were combined with methods to detect both gene and corresponding protein expression in different lung regions. Differential expression of mRNA by both airway level and lung region was determined for Clara cell secretory protein, calcitonin gene-related peptide, uteroglobin-related protein 2, surfactant protein A, and surfactant protein C. Therefore, for maximal enrichment of mRNA and maximal ability to identify changes in mRNA levels in the diseased state or in response to chemical exposure, it is critical to choose the appropriate airway region and sample collection method to enrich detection of the transcript(s) of interest. 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subjects | Animals Calcitonin Gene-Related Peptide - biosynthesis Calcitonin Gene-Related Peptide - genetics Calcitonin Gene-Related Peptide - secretion Gene Expression Profiling Immunohistochemistry Lung - metabolism Male Mice Organ Specificity Proteins - genetics Proteins - metabolism Proteins - secretion Pulmonary Surfactant-Associated Protein A - biosynthesis Pulmonary Surfactant-Associated Protein A - genetics Pulmonary Surfactant-Associated Protein A - secretion Pulmonary Surfactant-Associated Protein C - biosynthesis Pulmonary Surfactant-Associated Protein C - genetics Pulmonary Surfactant-Associated Protein C - secretion Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - biosynthesis RNA, Messenger - genetics Uteroglobin - biosynthesis Uteroglobin - genetics Uteroglobin - secretion |
title | Site-specific Differences in Gene Expression of Secreted Proteins in the Mouse Lung: Comparison of Methods to Show Differences by Location |
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