Layer-dependent role of collagen recruitment during loading of the rat bladder wall
In this work, we re-evaluated long-standing conjectures as to the source of the exceptionally large compliance of the bladder wall. Whereas these conjectures were based on indirect measures of loading mechanisms, in this work we take advantage of advances in bioimaging to directly assess collagen fi...
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creator | Cheng, Fangzhou Birder, Lori A. Kullmann, F. Aura Hornsby, Jack Watton, Paul N. Watkins, Simon Thompson, Mark Robertson, Anne M. |
description | In this work, we re-evaluated long-standing conjectures as to the source of the exceptionally large compliance of the bladder wall. Whereas these conjectures were based on indirect measures of loading mechanisms, in this work we take advantage of advances in bioimaging to directly assess collagen fibers and wall architecture during biaxial loading. A custom biaxial mechanical testing system compatible with multiphoton microscopy was used to directly measure the layer-dependent collagen fiber recruitment in bladder tissue from 9 male Fischer rats (4 adult and 5 aged). As for other soft tissues, the bladder loading curve was exponential in shape and could be divided into toe, transition and high stress regimes. The relationship between collagen recruitment and loading curves was evaluated in the context of the inner (lamina propria) and outer (detrusor smooth muscle) layers. The large extensibility of the bladder was found to be possible due to folds in the wall (rugae) that provide a mechanism for low resistance flattening without any discernible recruitment of collagen fibers throughout the toe regime. For more extensible bladders, as the loading extended into the transition regime, a gradual coordinated recruitment of collagen fibers between the lamina propria layer and detrusor smooth muscle layer was found. A second important finding was that wall extensibility could be lost by premature recruitment of collagen in the outer wall that cut short the toe region. This change was correlated with age. This work provides, for the first time, a mechanistic understanding of the role of collagen recruitment in determining bladder extensibility and capacitance. |
doi_str_mv | 10.1007/s10237-017-0968-5 |
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Aura ; Hornsby, Jack ; Watton, Paul N. ; Watkins, Simon ; Thompson, Mark ; Robertson, Anne M.</creator><creatorcontrib>Cheng, Fangzhou ; Birder, Lori A. ; Kullmann, F. Aura ; Hornsby, Jack ; Watton, Paul N. ; Watkins, Simon ; Thompson, Mark ; Robertson, Anne M.</creatorcontrib><description>In this work, we re-evaluated long-standing conjectures as to the source of the exceptionally large compliance of the bladder wall. Whereas these conjectures were based on indirect measures of loading mechanisms, in this work we take advantage of advances in bioimaging to directly assess collagen fibers and wall architecture during biaxial loading. A custom biaxial mechanical testing system compatible with multiphoton microscopy was used to directly measure the layer-dependent collagen fiber recruitment in bladder tissue from 9 male Fischer rats (4 adult and 5 aged). As for other soft tissues, the bladder loading curve was exponential in shape and could be divided into toe, transition and high stress regimes. The relationship between collagen recruitment and loading curves was evaluated in the context of the inner (lamina propria) and outer (detrusor smooth muscle) layers. The large extensibility of the bladder was found to be possible due to folds in the wall (rugae) that provide a mechanism for low resistance flattening without any discernible recruitment of collagen fibers throughout the toe regime. For more extensible bladders, as the loading extended into the transition regime, a gradual coordinated recruitment of collagen fibers between the lamina propria layer and detrusor smooth muscle layer was found. A second important finding was that wall extensibility could be lost by premature recruitment of collagen in the outer wall that cut short the toe region. This change was correlated with age. This work provides, for the first time, a mechanistic understanding of the role of collagen recruitment in determining bladder extensibility and capacitance.</description><identifier>ISSN: 1617-7959</identifier><identifier>EISSN: 1617-7940</identifier><identifier>DOI: 10.1007/s10237-017-0968-5</identifier><identifier>PMID: 29039043</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Biaxial loads ; Biological and Medical Physics ; Biomechanical Phenomena ; Biomedical Engineering and Bioengineering ; Biophysics ; Bladder ; Capacitance ; Collagen ; Collagen - metabolism ; Compliance ; Engineering ; Extensibility ; Fibers ; Lamina propria ; Low resistance ; Male ; Mechanical properties ; Mechanical tests ; Medical imaging ; Microscopy, Fluorescence, Multiphoton ; Mucous Membrane - metabolism ; Muscle, Smooth - metabolism ; Muscles ; Original Paper ; Rats ; Rats, Inbred F344 ; Recruitment ; Rodents ; Smooth muscle ; Soft tissues ; Stress, Mechanical ; Theoretical and Applied Mechanics ; Urinary bladder ; Urinary Bladder - metabolism ; Weight-Bearing</subject><ispartof>Biomechanics and modeling in mechanobiology, 2018-04, Vol.17 (2), p.403-417</ispartof><rights>Springer-Verlag GmbH Germany 2017</rights><rights>Biomechanics and Modeling in Mechanobiology is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-a1bfa35ff2f566867ff110138966279de3e3f7f4ef9fb03ae82d04274d6b66723</citedby><cites>FETCH-LOGICAL-c507t-a1bfa35ff2f566867ff110138966279de3e3f7f4ef9fb03ae82d04274d6b66723</cites><orcidid>0000-0002-5063-4293</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10237-017-0968-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10237-017-0968-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29039043$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheng, Fangzhou</creatorcontrib><creatorcontrib>Birder, Lori A.</creatorcontrib><creatorcontrib>Kullmann, F. Aura</creatorcontrib><creatorcontrib>Hornsby, Jack</creatorcontrib><creatorcontrib>Watton, Paul N.</creatorcontrib><creatorcontrib>Watkins, Simon</creatorcontrib><creatorcontrib>Thompson, Mark</creatorcontrib><creatorcontrib>Robertson, Anne M.</creatorcontrib><title>Layer-dependent role of collagen recruitment during loading of the rat bladder wall</title><title>Biomechanics and modeling in mechanobiology</title><addtitle>Biomech Model Mechanobiol</addtitle><addtitle>Biomech Model Mechanobiol</addtitle><description>In this work, we re-evaluated long-standing conjectures as to the source of the exceptionally large compliance of the bladder wall. Whereas these conjectures were based on indirect measures of loading mechanisms, in this work we take advantage of advances in bioimaging to directly assess collagen fibers and wall architecture during biaxial loading. A custom biaxial mechanical testing system compatible with multiphoton microscopy was used to directly measure the layer-dependent collagen fiber recruitment in bladder tissue from 9 male Fischer rats (4 adult and 5 aged). As for other soft tissues, the bladder loading curve was exponential in shape and could be divided into toe, transition and high stress regimes. The relationship between collagen recruitment and loading curves was evaluated in the context of the inner (lamina propria) and outer (detrusor smooth muscle) layers. The large extensibility of the bladder was found to be possible due to folds in the wall (rugae) that provide a mechanism for low resistance flattening without any discernible recruitment of collagen fibers throughout the toe regime. For more extensible bladders, as the loading extended into the transition regime, a gradual coordinated recruitment of collagen fibers between the lamina propria layer and detrusor smooth muscle layer was found. A second important finding was that wall extensibility could be lost by premature recruitment of collagen in the outer wall that cut short the toe region. This change was correlated with age. This work provides, for the first time, a mechanistic understanding of the role of collagen recruitment in determining bladder extensibility and capacitance.</description><subject>Animals</subject><subject>Biaxial loads</subject><subject>Biological and Medical Physics</subject><subject>Biomechanical Phenomena</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biophysics</subject><subject>Bladder</subject><subject>Capacitance</subject><subject>Collagen</subject><subject>Collagen - metabolism</subject><subject>Compliance</subject><subject>Engineering</subject><subject>Extensibility</subject><subject>Fibers</subject><subject>Lamina propria</subject><subject>Low resistance</subject><subject>Male</subject><subject>Mechanical properties</subject><subject>Mechanical tests</subject><subject>Medical imaging</subject><subject>Microscopy, Fluorescence, Multiphoton</subject><subject>Mucous Membrane - metabolism</subject><subject>Muscle, Smooth - metabolism</subject><subject>Muscles</subject><subject>Original Paper</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Recruitment</subject><subject>Rodents</subject><subject>Smooth muscle</subject><subject>Soft tissues</subject><subject>Stress, Mechanical</subject><subject>Theoretical and Applied Mechanics</subject><subject>Urinary bladder</subject><subject>Urinary Bladder - metabolism</subject><subject>Weight-Bearing</subject><issn>1617-7959</issn><issn>1617-7940</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kU1v3CAQhlHUKp_9Ab1Ulnrpxe0ABswlUhS1TaWVckhyRtgMG0es2YLdKv8-WJtu20g5wIDmmZcZXkLeU_hMAdSXTIFxVQMtS8u2FgfkmMpyU7qBN_uz0EfkJOcHAAa85YfkiGngGhp-TG5W9hFT7XCLo8NxqlIMWEVf9TEEu8axStineZg2S9LNaRjXVYjWLbFg0z1WyU5VF6xzmKrfNoQz8tbbkPHdczwld9--3l5e1avr7z8uL1Z1L0BNtaWdt1x4z7yQspXKe0qB8lZLyZR2yJF75Rv02nfALbbMQcNU42QnpWL8lJzvdLdzt0HXlw6TDWabho1NjybawfyfGYd7s46_jGgb0ShZBD49C6T4c8Y8mc2QeyyDjxjnbKgWDHTZVEE_vkAf4pzGMp5hQIWgqm0WQbqj-hRzTuj3zVAwi2VmZ5kplpnFMiNKzYd_p9hX_PGoAGwH5O3y-5j-Pv266hPdKaH3</recordid><startdate>20180401</startdate><enddate>20180401</enddate><creator>Cheng, Fangzhou</creator><creator>Birder, Lori A.</creator><creator>Kullmann, F. 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Aura ; Hornsby, Jack ; Watton, Paul N. ; Watkins, Simon ; Thompson, Mark ; Robertson, Anne M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-a1bfa35ff2f566867ff110138966279de3e3f7f4ef9fb03ae82d04274d6b66723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Biaxial loads</topic><topic>Biological and Medical Physics</topic><topic>Biomechanical Phenomena</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biophysics</topic><topic>Bladder</topic><topic>Capacitance</topic><topic>Collagen</topic><topic>Collagen - metabolism</topic><topic>Compliance</topic><topic>Engineering</topic><topic>Extensibility</topic><topic>Fibers</topic><topic>Lamina propria</topic><topic>Low resistance</topic><topic>Male</topic><topic>Mechanical properties</topic><topic>Mechanical tests</topic><topic>Medical imaging</topic><topic>Microscopy, Fluorescence, Multiphoton</topic><topic>Mucous Membrane - metabolism</topic><topic>Muscle, Smooth - metabolism</topic><topic>Muscles</topic><topic>Original Paper</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Recruitment</topic><topic>Rodents</topic><topic>Smooth muscle</topic><topic>Soft tissues</topic><topic>Stress, Mechanical</topic><topic>Theoretical and Applied Mechanics</topic><topic>Urinary bladder</topic><topic>Urinary Bladder - metabolism</topic><topic>Weight-Bearing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheng, Fangzhou</creatorcontrib><creatorcontrib>Birder, Lori A.</creatorcontrib><creatorcontrib>Kullmann, F. 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Aura</au><au>Hornsby, Jack</au><au>Watton, Paul N.</au><au>Watkins, Simon</au><au>Thompson, Mark</au><au>Robertson, Anne M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Layer-dependent role of collagen recruitment during loading of the rat bladder wall</atitle><jtitle>Biomechanics and modeling in mechanobiology</jtitle><stitle>Biomech Model Mechanobiol</stitle><addtitle>Biomech Model Mechanobiol</addtitle><date>2018-04-01</date><risdate>2018</risdate><volume>17</volume><issue>2</issue><spage>403</spage><epage>417</epage><pages>403-417</pages><issn>1617-7959</issn><eissn>1617-7940</eissn><abstract>In this work, we re-evaluated long-standing conjectures as to the source of the exceptionally large compliance of the bladder wall. Whereas these conjectures were based on indirect measures of loading mechanisms, in this work we take advantage of advances in bioimaging to directly assess collagen fibers and wall architecture during biaxial loading. A custom biaxial mechanical testing system compatible with multiphoton microscopy was used to directly measure the layer-dependent collagen fiber recruitment in bladder tissue from 9 male Fischer rats (4 adult and 5 aged). As for other soft tissues, the bladder loading curve was exponential in shape and could be divided into toe, transition and high stress regimes. The relationship between collagen recruitment and loading curves was evaluated in the context of the inner (lamina propria) and outer (detrusor smooth muscle) layers. The large extensibility of the bladder was found to be possible due to folds in the wall (rugae) that provide a mechanism for low resistance flattening without any discernible recruitment of collagen fibers throughout the toe regime. For more extensible bladders, as the loading extended into the transition regime, a gradual coordinated recruitment of collagen fibers between the lamina propria layer and detrusor smooth muscle layer was found. A second important finding was that wall extensibility could be lost by premature recruitment of collagen in the outer wall that cut short the toe region. This change was correlated with age. This work provides, for the first time, a mechanistic understanding of the role of collagen recruitment in determining bladder extensibility and capacitance.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>29039043</pmid><doi>10.1007/s10237-017-0968-5</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-5063-4293</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biaxial loads Biological and Medical Physics Biomechanical Phenomena Biomedical Engineering and Bioengineering Biophysics Bladder Capacitance Collagen Collagen - metabolism Compliance Engineering Extensibility Fibers Lamina propria Low resistance Male Mechanical properties Mechanical tests Medical imaging Microscopy, Fluorescence, Multiphoton Mucous Membrane - metabolism Muscle, Smooth - metabolism Muscles Original Paper Rats Rats, Inbred F344 Recruitment Rodents Smooth muscle Soft tissues Stress, Mechanical Theoretical and Applied Mechanics Urinary bladder Urinary Bladder - metabolism Weight-Bearing |
title | Layer-dependent role of collagen recruitment during loading of the rat bladder wall |
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