Basement membrane integrity and keratinization in healthy and ulcerated bovine hoof tissue
Damage to, or deterioration of, the keratinized horn tissue of the bovine hoof claw culminates ultimately in the development of solear ulceration. We have observed abnormal keratin distribution at the site of solear ulceration in the bovine claw that may be due to alteration of the positional cues o...
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description | Damage to, or deterioration of, the keratinized horn tissue of the bovine hoof claw culminates ultimately in the development of solear ulceration. We have observed abnormal keratin distribution at the site of solear ulceration in the bovine claw that may be due to alteration of the positional cues of the keratinocytes. In this study we have characterized key cell biological changes associated with ulceration in the claw that may precipitate abnormal keratinization. Loss of basement membrane at sites of ulceration was found by immunofluorescent detection of laminin and integrins. In other tissues, basement membrane breakdown results from degradation by matrix metalloproteinases (MMPs). Similarly, elevated levels of MMPs 2 and 9 were observed in ulcerated bovine claw tissue both by zymography and, quantitatively, by assay of enzyme activity. In the sole of claws that contained an ulcer, tissue distal to the ulcer site also had elevated MMP 2 when compared with healthy sole tissue from the same animals, as did sole tissue of claws recovering from ulceration. Tissue inhibitor of metalloproteinase 2 (TIMP 2) was detected by ELISA in healthy tissue. TIMP 2 tended to be lower in diseased tissue distal to ulcer sites, and was significantly lower in ulcerated tissue. MMP 2 was located by immunofluorescence in the dermal and basal epidermal region of sole tissue, in the region of the basement membrane. Increased punctate staining of material in the dermis was associated with ulcerated material. ELISA of TIMP 2 in tissue extracts enriched for dermis or epidermis confirmed that the inhibitor was located predominantly in the dermis. To investigate a possible causal relationship between basement membrane anchorage and epidermal keratinization, the effect of function-blocking antibodies to laminins and integrins was tested in tissue explant cultures prepared from healthy sole tissue. Anti-integrin antibody treatment had no effect on either protein or DNA synthesis. In contrast, in the presence of anti-laminin antibody, protein synthesis was decreased in a concentration-dependent manner, a significant effect being observed at the highest concentration after treatment for 24 h. At this concentration, DNA synthesis was also decreased after 48 h of culture, an effect that may be relevant to a hibernal reduction in claw cell turnover, and the associated seasonal vulnerability of cows to claw damage. The results provide evidence for basement membrane disruption at ulcer sites, |
doi_str_mv | 10.1017/S0022029902005885 |
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We have observed abnormal keratin distribution at the site of solear ulceration in the bovine claw that may be due to alteration of the positional cues of the keratinocytes. In this study we have characterized key cell biological changes associated with ulceration in the claw that may precipitate abnormal keratinization. Loss of basement membrane at sites of ulceration was found by immunofluorescent detection of laminin and integrins. In other tissues, basement membrane breakdown results from degradation by matrix metalloproteinases (MMPs). Similarly, elevated levels of MMPs 2 and 9 were observed in ulcerated bovine claw tissue both by zymography and, quantitatively, by assay of enzyme activity. In the sole of claws that contained an ulcer, tissue distal to the ulcer site also had elevated MMP 2 when compared with healthy sole tissue from the same animals, as did sole tissue of claws recovering from ulceration. Tissue inhibitor of metalloproteinase 2 (TIMP 2) was detected by ELISA in healthy tissue. TIMP 2 tended to be lower in diseased tissue distal to ulcer sites, and was significantly lower in ulcerated tissue. MMP 2 was located by immunofluorescence in the dermal and basal epidermal region of sole tissue, in the region of the basement membrane. Increased punctate staining of material in the dermis was associated with ulcerated material. ELISA of TIMP 2 in tissue extracts enriched for dermis or epidermis confirmed that the inhibitor was located predominantly in the dermis. To investigate a possible causal relationship between basement membrane anchorage and epidermal keratinization, the effect of function-blocking antibodies to laminins and integrins was tested in tissue explant cultures prepared from healthy sole tissue. Anti-integrin antibody treatment had no effect on either protein or DNA synthesis. In contrast, in the presence of anti-laminin antibody, protein synthesis was decreased in a concentration-dependent manner, a significant effect being observed at the highest concentration after treatment for 24 h. At this concentration, DNA synthesis was also decreased after 48 h of culture, an effect that may be relevant to a hibernal reduction in claw cell turnover, and the associated seasonal vulnerability of cows to claw damage. The results provide evidence for basement membrane disruption at ulcer sites, and an increased potential for disruption in the diseased claw, and a causal link between this and abnormal epidermal keratinization. Basement membrane disruption is in turn associated with reciprocal changes in MMPs and their inhibitors, favouring extracellular proteolysis. Whether MMP activation is the primary cause of dermal–epidermal deterioration and, if so, how MMP activation is triggered, remains to be determined.</description><identifier>ISSN: 0022-0299</identifier><identifier>EISSN: 1469-7629</identifier><identifier>DOI: 10.1017/S0022029902005885</identifier><identifier>PMID: 12617389</identifier><identifier>CODEN: JDRSAN</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Animal productions ; Animals ; Basement Membrane - pathology ; Biological and medical sciences ; Cattle ; Cattle Diseases - metabolism ; Cattle Diseases - pathology ; cow ; Deoxyribonucleic acid ; DNA ; Enzymatic activity ; Enzyme-Linked Immunosorbent Assay ; Epidermis ; Fluorescent Antibody Technique ; Foot Ulcer - metabolism ; Foot Ulcer - pathology ; Foot Ulcer - veterinary ; Fundamental and applied biological sciences. Psychology ; Hoof ; Hoof and Claw - chemistry ; Hoof and Claw - metabolism ; Hoof and Claw - pathology ; keratinocytes ; Keratins - metabolism ; lameness ; Matrix Metalloproteinase 2 - analysis ; Matrix Metalloproteinase 2 - metabolism ; Matrix Metalloproteinase 9 - metabolism ; Medical sciences ; Membranes ; Microscopy, Fluorescence ; MMPs ; Protein synthesis ; Signal Transduction ; Terrestrial animal productions ; TIMPs ; Tissue Distribution ; Tissue Inhibitor of Metalloproteinase-2 - analysis ; Tissues ; Traumas. Diseases due to physical agents ; ulceration ; Vascular injuries: limbs, aorta, vena cava ; Vertebrates</subject><ispartof>Journal of dairy research, 2003-02, Vol.70 (1), p.19-27</ispartof><rights>Proprietors of Journal of Dairy Research 2003</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-df3633afd1ec1eef3954c63c07af985f62cee1bce2fcf6491d94728bc39dfd483</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0022029902005885/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>164,314,776,780,27903,27904,55607</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14552927$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12617389$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hendry, Kay AK</creatorcontrib><creatorcontrib>Knight, Christopher H</creatorcontrib><creatorcontrib>Galbraith, Hugh</creatorcontrib><creatorcontrib>Wilde, Colin J</creatorcontrib><title>Basement membrane integrity and keratinization in healthy and ulcerated bovine hoof tissue</title><title>Journal of dairy research</title><addtitle>Journal of Dairy Research</addtitle><description>Damage to, or deterioration of, the keratinized horn tissue of the bovine hoof claw culminates ultimately in the development of solear ulceration. We have observed abnormal keratin distribution at the site of solear ulceration in the bovine claw that may be due to alteration of the positional cues of the keratinocytes. In this study we have characterized key cell biological changes associated with ulceration in the claw that may precipitate abnormal keratinization. Loss of basement membrane at sites of ulceration was found by immunofluorescent detection of laminin and integrins. In other tissues, basement membrane breakdown results from degradation by matrix metalloproteinases (MMPs). Similarly, elevated levels of MMPs 2 and 9 were observed in ulcerated bovine claw tissue both by zymography and, quantitatively, by assay of enzyme activity. In the sole of claws that contained an ulcer, tissue distal to the ulcer site also had elevated MMP 2 when compared with healthy sole tissue from the same animals, as did sole tissue of claws recovering from ulceration. Tissue inhibitor of metalloproteinase 2 (TIMP 2) was detected by ELISA in healthy tissue. TIMP 2 tended to be lower in diseased tissue distal to ulcer sites, and was significantly lower in ulcerated tissue. MMP 2 was located by immunofluorescence in the dermal and basal epidermal region of sole tissue, in the region of the basement membrane. Increased punctate staining of material in the dermis was associated with ulcerated material. ELISA of TIMP 2 in tissue extracts enriched for dermis or epidermis confirmed that the inhibitor was located predominantly in the dermis. To investigate a possible causal relationship between basement membrane anchorage and epidermal keratinization, the effect of function-blocking antibodies to laminins and integrins was tested in tissue explant cultures prepared from healthy sole tissue. Anti-integrin antibody treatment had no effect on either protein or DNA synthesis. In contrast, in the presence of anti-laminin antibody, protein synthesis was decreased in a concentration-dependent manner, a significant effect being observed at the highest concentration after treatment for 24 h. At this concentration, DNA synthesis was also decreased after 48 h of culture, an effect that may be relevant to a hibernal reduction in claw cell turnover, and the associated seasonal vulnerability of cows to claw damage. The results provide evidence for basement membrane disruption at ulcer sites, and an increased potential for disruption in the diseased claw, and a causal link between this and abnormal epidermal keratinization. Basement membrane disruption is in turn associated with reciprocal changes in MMPs and their inhibitors, favouring extracellular proteolysis. Whether MMP activation is the primary cause of dermal–epidermal deterioration and, if so, how MMP activation is triggered, remains to be determined.</description><subject>Animal productions</subject><subject>Animals</subject><subject>Basement Membrane - pathology</subject><subject>Biological and medical sciences</subject><subject>Cattle</subject><subject>Cattle Diseases - metabolism</subject><subject>Cattle Diseases - pathology</subject><subject>cow</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Enzymatic activity</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Epidermis</subject><subject>Fluorescent Antibody Technique</subject><subject>Foot Ulcer - metabolism</subject><subject>Foot Ulcer - pathology</subject><subject>Foot Ulcer - veterinary</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hoof</subject><subject>Hoof and Claw - chemistry</subject><subject>Hoof and Claw - metabolism</subject><subject>Hoof and Claw - pathology</subject><subject>keratinocytes</subject><subject>Keratins - metabolism</subject><subject>lameness</subject><subject>Matrix Metalloproteinase 2 - analysis</subject><subject>Matrix Metalloproteinase 2 - metabolism</subject><subject>Matrix Metalloproteinase 9 - metabolism</subject><subject>Medical sciences</subject><subject>Membranes</subject><subject>Microscopy, Fluorescence</subject><subject>MMPs</subject><subject>Protein synthesis</subject><subject>Signal Transduction</subject><subject>Terrestrial animal productions</subject><subject>TIMPs</subject><subject>Tissue Distribution</subject><subject>Tissue Inhibitor of Metalloproteinase-2 - analysis</subject><subject>Tissues</subject><subject>Traumas. Diseases due to physical agents</subject><subject>ulceration</subject><subject>Vascular injuries: limbs, aorta, vena cava</subject><subject>Vertebrates</subject><issn>0022-0299</issn><issn>1469-7629</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</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>eNp1kVtrFTEUhYMo9lj9Ab7IIOjbtLlMksmjp9oLtIioFHwJmWSnJ-1capIR6683hzN4QPEleVjf2qy9NkIvCT4imMjjzxhTiqlSmGLM25Y_QivSCFVLQdVjtNrK9VY_QM9SusWYMKzEU3RAqCCStWqFvq1NggHGXA0wdNGMUIUxw00M-aEyo6vuIJocxvCrvNNYxGoDps-bnTr3dquDq7rpRyjmzTT5KoeUZniOnnjTJ3ix_Ifo6-mHLyfn9eXHs4uTd5e1bZjItfNMMGa8I2AJgGeKN1Ywi6XxquVeUAtAOgvUWy8aRZxqJG07y5TzrmnZIXq7m3sfp-8zpKyHkCz0fVlmmpOWDEvWMFLA13-Bt9Mcx5JNUyoVl5yoApEdZOOUUgSv72MYTHzQBOtt6_qf1ovn1TJ47gZwe8dScwHeLIBJ1vS-9GxD2nMN51RRWbh6x4WU4ecf3cQ7LSSTXIuzT3r9_pxfra9P9XXh2RLWlOMFdwP7lf4f9zcVH6lB</recordid><startdate>20030201</startdate><enddate>20030201</enddate><creator>Hendry, Kay AK</creator><creator>Knight, Christopher H</creator><creator>Galbraith, Hugh</creator><creator>Wilde, Colin J</creator><general>Cambridge University Press</general><scope>BSCLL</scope><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>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7QR</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7U7</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7S</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>7X8</scope></search><sort><creationdate>20030201</creationdate><title>Basement membrane integrity and keratinization in healthy and ulcerated bovine hoof tissue</title><author>Hendry, Kay AK ; Knight, Christopher H ; Galbraith, Hugh ; Wilde, Colin J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-df3633afd1ec1eef3954c63c07af985f62cee1bce2fcf6491d94728bc39dfd483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animal productions</topic><topic>Animals</topic><topic>Basement Membrane - pathology</topic><topic>Biological and medical sciences</topic><topic>Cattle</topic><topic>Cattle Diseases - metabolism</topic><topic>Cattle Diseases - pathology</topic><topic>cow</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Enzymatic activity</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Epidermis</topic><topic>Fluorescent Antibody Technique</topic><topic>Foot Ulcer - metabolism</topic><topic>Foot Ulcer - pathology</topic><topic>Foot Ulcer - veterinary</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hoof</topic><topic>Hoof and Claw - chemistry</topic><topic>Hoof and Claw - metabolism</topic><topic>Hoof and Claw - pathology</topic><topic>keratinocytes</topic><topic>Keratins - metabolism</topic><topic>lameness</topic><topic>Matrix Metalloproteinase 2 - analysis</topic><topic>Matrix Metalloproteinase 2 - metabolism</topic><topic>Matrix Metalloproteinase 9 - metabolism</topic><topic>Medical sciences</topic><topic>Membranes</topic><topic>Microscopy, Fluorescence</topic><topic>MMPs</topic><topic>Protein synthesis</topic><topic>Signal Transduction</topic><topic>Terrestrial animal productions</topic><topic>TIMPs</topic><topic>Tissue Distribution</topic><topic>Tissue Inhibitor of Metalloproteinase-2 - analysis</topic><topic>Tissues</topic><topic>Traumas. Diseases due to physical agents</topic><topic>ulceration</topic><topic>Vascular injuries: limbs, aorta, vena cava</topic><topic>Vertebrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hendry, Kay AK</creatorcontrib><creatorcontrib>Knight, Christopher H</creatorcontrib><creatorcontrib>Galbraith, Hugh</creatorcontrib><creatorcontrib>Wilde, Colin J</creatorcontrib><collection>Istex</collection><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>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Engineering Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of dairy research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hendry, Kay AK</au><au>Knight, Christopher H</au><au>Galbraith, Hugh</au><au>Wilde, Colin J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Basement membrane integrity and keratinization in healthy and ulcerated bovine hoof tissue</atitle><jtitle>Journal of dairy research</jtitle><addtitle>Journal of Dairy Research</addtitle><date>2003-02-01</date><risdate>2003</risdate><volume>70</volume><issue>1</issue><spage>19</spage><epage>27</epage><pages>19-27</pages><issn>0022-0299</issn><eissn>1469-7629</eissn><coden>JDRSAN</coden><abstract>Damage to, or deterioration of, the keratinized horn tissue of the bovine hoof claw culminates ultimately in the development of solear ulceration. We have observed abnormal keratin distribution at the site of solear ulceration in the bovine claw that may be due to alteration of the positional cues of the keratinocytes. In this study we have characterized key cell biological changes associated with ulceration in the claw that may precipitate abnormal keratinization. Loss of basement membrane at sites of ulceration was found by immunofluorescent detection of laminin and integrins. In other tissues, basement membrane breakdown results from degradation by matrix metalloproteinases (MMPs). Similarly, elevated levels of MMPs 2 and 9 were observed in ulcerated bovine claw tissue both by zymography and, quantitatively, by assay of enzyme activity. In the sole of claws that contained an ulcer, tissue distal to the ulcer site also had elevated MMP 2 when compared with healthy sole tissue from the same animals, as did sole tissue of claws recovering from ulceration. Tissue inhibitor of metalloproteinase 2 (TIMP 2) was detected by ELISA in healthy tissue. TIMP 2 tended to be lower in diseased tissue distal to ulcer sites, and was significantly lower in ulcerated tissue. MMP 2 was located by immunofluorescence in the dermal and basal epidermal region of sole tissue, in the region of the basement membrane. Increased punctate staining of material in the dermis was associated with ulcerated material. ELISA of TIMP 2 in tissue extracts enriched for dermis or epidermis confirmed that the inhibitor was located predominantly in the dermis. To investigate a possible causal relationship between basement membrane anchorage and epidermal keratinization, the effect of function-blocking antibodies to laminins and integrins was tested in tissue explant cultures prepared from healthy sole tissue. Anti-integrin antibody treatment had no effect on either protein or DNA synthesis. In contrast, in the presence of anti-laminin antibody, protein synthesis was decreased in a concentration-dependent manner, a significant effect being observed at the highest concentration after treatment for 24 h. At this concentration, DNA synthesis was also decreased after 48 h of culture, an effect that may be relevant to a hibernal reduction in claw cell turnover, and the associated seasonal vulnerability of cows to claw damage. The results provide evidence for basement membrane disruption at ulcer sites, and an increased potential for disruption in the diseased claw, and a causal link between this and abnormal epidermal keratinization. Basement membrane disruption is in turn associated with reciprocal changes in MMPs and their inhibitors, favouring extracellular proteolysis. Whether MMP activation is the primary cause of dermal–epidermal deterioration and, if so, how MMP activation is triggered, remains to be determined.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>12617389</pmid><doi>10.1017/S0022029902005885</doi><tpages>9</tpages></addata></record> |
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subjects | Animal productions Animals Basement Membrane - pathology Biological and medical sciences Cattle Cattle Diseases - metabolism Cattle Diseases - pathology cow Deoxyribonucleic acid DNA Enzymatic activity Enzyme-Linked Immunosorbent Assay Epidermis Fluorescent Antibody Technique Foot Ulcer - metabolism Foot Ulcer - pathology Foot Ulcer - veterinary Fundamental and applied biological sciences. Psychology Hoof Hoof and Claw - chemistry Hoof and Claw - metabolism Hoof and Claw - pathology keratinocytes Keratins - metabolism lameness Matrix Metalloproteinase 2 - analysis Matrix Metalloproteinase 2 - metabolism Matrix Metalloproteinase 9 - metabolism Medical sciences Membranes Microscopy, Fluorescence MMPs Protein synthesis Signal Transduction Terrestrial animal productions TIMPs Tissue Distribution Tissue Inhibitor of Metalloproteinase-2 - analysis Tissues Traumas. Diseases due to physical agents ulceration Vascular injuries: limbs, aorta, vena cava Vertebrates |
title | Basement membrane integrity and keratinization in healthy and ulcerated bovine hoof tissue |
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