GaAlAs Laser Irradiation Induces Active Tertiary Dentin Formation after Pulpal Apoptosis and Cell Proliferation in Rat Molars
Abstract Introduction This study aimed to clarify pulpal responses to gallium-aluminum-arsenide (GaAlAs) laser irradiation. Methods Maxillary first molars of 8-week-old rats were irradiated at an output power of 0.5 or 1.5 W for 180 seconds, and the samples were collected at intervals of 0 to 14 day...
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description | Abstract Introduction This study aimed to clarify pulpal responses to gallium-aluminum-arsenide (GaAlAs) laser irradiation. Methods Maxillary first molars of 8-week-old rats were irradiated at an output power of 0.5 or 1.5 W for 180 seconds, and the samples were collected at intervals of 0 to 14 days. The demineralized paraffin sections were processed for immunohistochemistry for heat-shock protein (HSP)-25 and nestin in addition to cell proliferation assay using bromodeoxyuridine (BrdU) labeling and apoptosis assay using deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL). Results Intense HSP-25 and nestin immunoreactivities in the odontoblast layer were weakened immediately after 0.5-W irradiation and recovered on day 1, resulting in slight tertiary dentin formation by day 14. On the contrary, 1.5-W irradiation immediately induced the loss of HSP-25 and nestin-immunoreactivities in the odontoblast layer. On day 1, numerous TUNEL-positive cells appeared in a degenerative zone that was surrounded by intense HSP-25 immunoreactivity. BrdU-positive cells occurred within the intensely HSP-25–immunopositive areas during days 2 through 5, whereas TUNEL-positive cells gradually decreased in number by day 5. HSP-25– and nestin-positive odontoblast-like cells were arranged along the pulp-dentin border by day 7, resulting in remarkable tertiary dentin formation on day 14. Conclusions The output energy determined pulpal healing patterns after GaAlAs laser irradiation; the higher energy induced the apoptosis in the affected dental pulp including odontoblasts followed by active cell proliferation in the intense HSP-25–immunoreactive areas surrounding the degenerative tissue, resulting in abundant tertiary dentin formation. Thus, the optimal GaAlAs laser irradiation elicited intentional tertiary dentin formation in the dental pulp. |
doi_str_mv | 10.1016/j.joen.2011.05.020 |
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Methods Maxillary first molars of 8-week-old rats were irradiated at an output power of 0.5 or 1.5 W for 180 seconds, and the samples were collected at intervals of 0 to 14 days. The demineralized paraffin sections were processed for immunohistochemistry for heat-shock protein (HSP)-25 and nestin in addition to cell proliferation assay using bromodeoxyuridine (BrdU) labeling and apoptosis assay using deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL). Results Intense HSP-25 and nestin immunoreactivities in the odontoblast layer were weakened immediately after 0.5-W irradiation and recovered on day 1, resulting in slight tertiary dentin formation by day 14. On the contrary, 1.5-W irradiation immediately induced the loss of HSP-25 and nestin-immunoreactivities in the odontoblast layer. On day 1, numerous TUNEL-positive cells appeared in a degenerative zone that was surrounded by intense HSP-25 immunoreactivity. BrdU-positive cells occurred within the intensely HSP-25–immunopositive areas during days 2 through 5, whereas TUNEL-positive cells gradually decreased in number by day 5. HSP-25– and nestin-positive odontoblast-like cells were arranged along the pulp-dentin border by day 7, resulting in remarkable tertiary dentin formation on day 14. Conclusions The output energy determined pulpal healing patterns after GaAlAs laser irradiation; the higher energy induced the apoptosis in the affected dental pulp including odontoblasts followed by active cell proliferation in the intense HSP-25–immunoreactive areas surrounding the degenerative tissue, resulting in abundant tertiary dentin formation. Thus, the optimal GaAlAs laser irradiation elicited intentional tertiary dentin formation in the dental pulp.</description><identifier>ISSN: 0099-2399</identifier><identifier>EISSN: 1878-3554</identifier><identifier>DOI: 10.1016/j.joen.2011.05.020</identifier><identifier>PMID: 21763899</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Apoptosis ; Bromodeoxyuridine - metabolism ; Cell Proliferation ; dental pulp ; Dental Pulp - cytology ; Dental Pulp - physiology ; dentin ; Dentin, Secondary - secretion ; Dentistry ; Endocrinology & Metabolism ; Female ; heat-shock proteins ; HSP27 Heat-Shock Proteins - biosynthesis ; In Situ Nick-End Labeling ; Intermediate Filament Proteins - biosynthesis ; laser ; Lasers, Semiconductor - adverse effects ; Molar ; Nerve Tissue Proteins - biosynthesis ; Nestin ; odontoblasts ; Odontoblasts - physiology ; Rats ; Rats, Wistar ; Wound Healing</subject><ispartof>Journal of endodontics, 2011-08, Vol.37 (8), p.1086-1091</ispartof><rights>American Association of Endodontists</rights><rights>2011 American Association of Endodontists</rights><rights>Copyright © 2011 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-dde95ffe20ccf6c9493baa23df4de19142eb1a2c9b27c04d1f64dc9e2a1c2e363</citedby><cites>FETCH-LOGICAL-c476t-dde95ffe20ccf6c9493baa23df4de19142eb1a2c9b27c04d1f64dc9e2a1c2e363</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.joen.2011.05.020$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3541,27915,27916,45986</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21763899$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shigetani, Yoshimi, DDS, PhD</creatorcontrib><creatorcontrib>Sasa, Natsuki, DDS</creatorcontrib><creatorcontrib>Suzuki, Hironobu, DDS, PhD</creatorcontrib><creatorcontrib>Okiji, Takashi, DDS, PhD</creatorcontrib><creatorcontrib>Ohshima, Hayato, DDS, PhD</creatorcontrib><title>GaAlAs Laser Irradiation Induces Active Tertiary Dentin Formation after Pulpal Apoptosis and Cell Proliferation in Rat Molars</title><title>Journal of endodontics</title><addtitle>J Endod</addtitle><description>Abstract Introduction This study aimed to clarify pulpal responses to gallium-aluminum-arsenide (GaAlAs) laser irradiation. Methods Maxillary first molars of 8-week-old rats were irradiated at an output power of 0.5 or 1.5 W for 180 seconds, and the samples were collected at intervals of 0 to 14 days. The demineralized paraffin sections were processed for immunohistochemistry for heat-shock protein (HSP)-25 and nestin in addition to cell proliferation assay using bromodeoxyuridine (BrdU) labeling and apoptosis assay using deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL). Results Intense HSP-25 and nestin immunoreactivities in the odontoblast layer were weakened immediately after 0.5-W irradiation and recovered on day 1, resulting in slight tertiary dentin formation by day 14. On the contrary, 1.5-W irradiation immediately induced the loss of HSP-25 and nestin-immunoreactivities in the odontoblast layer. On day 1, numerous TUNEL-positive cells appeared in a degenerative zone that was surrounded by intense HSP-25 immunoreactivity. BrdU-positive cells occurred within the intensely HSP-25–immunopositive areas during days 2 through 5, whereas TUNEL-positive cells gradually decreased in number by day 5. HSP-25– and nestin-positive odontoblast-like cells were arranged along the pulp-dentin border by day 7, resulting in remarkable tertiary dentin formation on day 14. Conclusions The output energy determined pulpal healing patterns after GaAlAs laser irradiation; the higher energy induced the apoptosis in the affected dental pulp including odontoblasts followed by active cell proliferation in the intense HSP-25–immunoreactive areas surrounding the degenerative tissue, resulting in abundant tertiary dentin formation. Thus, the optimal GaAlAs laser irradiation elicited intentional tertiary dentin formation in the dental pulp.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Bromodeoxyuridine - metabolism</subject><subject>Cell Proliferation</subject><subject>dental pulp</subject><subject>Dental Pulp - cytology</subject><subject>Dental Pulp - physiology</subject><subject>dentin</subject><subject>Dentin, Secondary - secretion</subject><subject>Dentistry</subject><subject>Endocrinology & Metabolism</subject><subject>Female</subject><subject>heat-shock proteins</subject><subject>HSP27 Heat-Shock Proteins - biosynthesis</subject><subject>In Situ Nick-End Labeling</subject><subject>Intermediate Filament Proteins - biosynthesis</subject><subject>laser</subject><subject>Lasers, Semiconductor - adverse effects</subject><subject>Molar</subject><subject>Nerve Tissue Proteins - biosynthesis</subject><subject>Nestin</subject><subject>odontoblasts</subject><subject>Odontoblasts - physiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Wound Healing</subject><issn>0099-2399</issn><issn>1878-3554</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2LFDEQhoMo7rj6BzxIbp66zUd_TECEYdZdB0ZcdD2HTFINaTNJm6QX9uB_N02vHjx4qsvzvlQ9hdBrSmpKaPdurMcAvmaE0pq0NWHkCdrQbb-teNs2T9GGECEqxoW4QC9SGgmhPef9c3TBaN_xrRAb9OtG7dwu4aNKEPEhRmWsyjZ4fPBm1pDwTmd7D_gOYrYqPuAr8Nl6fB3ieQXVkEv0dnaTcng3hSmHZBNW3uA9OIdvY3B2gLjSJfpVZfw5OBXTS_RsUC7Bq8d5ib5ff7zbf6qOX24O-92x0k3f5coYEO0wACNaD50WjeAnpRg3Q2OACtowOFHFtDixXpPG0KFrjBbAFNUMeMcv0du1d4rh5wwpy7NNuiynPIQ5yeKMMNH0opBsJXUMKUUY5BTtudwtKZGLdTnKxbpcrEvSymK9hN481s-nM5i_kT-aC_B-BaAceW8hyqQteA3GRtBZmmD_3__hn7h21lut3A94gDSGOfqiT1KZmCTy2_L35e2UEtLRpuW_Ad4Aqoo</recordid><startdate>20110801</startdate><enddate>20110801</enddate><creator>Shigetani, Yoshimi, DDS, PhD</creator><creator>Sasa, Natsuki, DDS</creator><creator>Suzuki, Hironobu, DDS, PhD</creator><creator>Okiji, Takashi, DDS, PhD</creator><creator>Ohshima, Hayato, DDS, PhD</creator><general>Elsevier Inc</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></search><sort><creationdate>20110801</creationdate><title>GaAlAs Laser Irradiation Induces Active Tertiary Dentin Formation after Pulpal Apoptosis and Cell Proliferation in Rat Molars</title><author>Shigetani, Yoshimi, DDS, PhD ; Sasa, Natsuki, DDS ; Suzuki, Hironobu, DDS, PhD ; Okiji, Takashi, DDS, PhD ; Ohshima, Hayato, DDS, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-dde95ffe20ccf6c9493baa23df4de19142eb1a2c9b27c04d1f64dc9e2a1c2e363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Bromodeoxyuridine - metabolism</topic><topic>Cell Proliferation</topic><topic>dental pulp</topic><topic>Dental Pulp - cytology</topic><topic>Dental Pulp - physiology</topic><topic>dentin</topic><topic>Dentin, Secondary - secretion</topic><topic>Dentistry</topic><topic>Endocrinology & Metabolism</topic><topic>Female</topic><topic>heat-shock proteins</topic><topic>HSP27 Heat-Shock Proteins - biosynthesis</topic><topic>In Situ Nick-End Labeling</topic><topic>Intermediate Filament Proteins - biosynthesis</topic><topic>laser</topic><topic>Lasers, Semiconductor - adverse effects</topic><topic>Molar</topic><topic>Nerve Tissue Proteins - biosynthesis</topic><topic>Nestin</topic><topic>odontoblasts</topic><topic>Odontoblasts - physiology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Wound Healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shigetani, Yoshimi, DDS, PhD</creatorcontrib><creatorcontrib>Sasa, Natsuki, DDS</creatorcontrib><creatorcontrib>Suzuki, Hironobu, DDS, PhD</creatorcontrib><creatorcontrib>Okiji, Takashi, DDS, PhD</creatorcontrib><creatorcontrib>Ohshima, Hayato, DDS, PhD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of endodontics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shigetani, Yoshimi, DDS, PhD</au><au>Sasa, Natsuki, DDS</au><au>Suzuki, Hironobu, DDS, PhD</au><au>Okiji, Takashi, DDS, PhD</au><au>Ohshima, Hayato, DDS, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GaAlAs Laser Irradiation Induces Active Tertiary Dentin Formation after Pulpal Apoptosis and Cell Proliferation in Rat Molars</atitle><jtitle>Journal of endodontics</jtitle><addtitle>J Endod</addtitle><date>2011-08-01</date><risdate>2011</risdate><volume>37</volume><issue>8</issue><spage>1086</spage><epage>1091</epage><pages>1086-1091</pages><issn>0099-2399</issn><eissn>1878-3554</eissn><abstract>Abstract Introduction This study aimed to clarify pulpal responses to gallium-aluminum-arsenide (GaAlAs) laser irradiation. Methods Maxillary first molars of 8-week-old rats were irradiated at an output power of 0.5 or 1.5 W for 180 seconds, and the samples were collected at intervals of 0 to 14 days. The demineralized paraffin sections were processed for immunohistochemistry for heat-shock protein (HSP)-25 and nestin in addition to cell proliferation assay using bromodeoxyuridine (BrdU) labeling and apoptosis assay using deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL). Results Intense HSP-25 and nestin immunoreactivities in the odontoblast layer were weakened immediately after 0.5-W irradiation and recovered on day 1, resulting in slight tertiary dentin formation by day 14. On the contrary, 1.5-W irradiation immediately induced the loss of HSP-25 and nestin-immunoreactivities in the odontoblast layer. On day 1, numerous TUNEL-positive cells appeared in a degenerative zone that was surrounded by intense HSP-25 immunoreactivity. BrdU-positive cells occurred within the intensely HSP-25–immunopositive areas during days 2 through 5, whereas TUNEL-positive cells gradually decreased in number by day 5. HSP-25– and nestin-positive odontoblast-like cells were arranged along the pulp-dentin border by day 7, resulting in remarkable tertiary dentin formation on day 14. Conclusions The output energy determined pulpal healing patterns after GaAlAs laser irradiation; the higher energy induced the apoptosis in the affected dental pulp including odontoblasts followed by active cell proliferation in the intense HSP-25–immunoreactive areas surrounding the degenerative tissue, resulting in abundant tertiary dentin formation. Thus, the optimal GaAlAs laser irradiation elicited intentional tertiary dentin formation in the dental pulp.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21763899</pmid><doi>10.1016/j.joen.2011.05.020</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Apoptosis Bromodeoxyuridine - metabolism Cell Proliferation dental pulp Dental Pulp - cytology Dental Pulp - physiology dentin Dentin, Secondary - secretion Dentistry Endocrinology & Metabolism Female heat-shock proteins HSP27 Heat-Shock Proteins - biosynthesis In Situ Nick-End Labeling Intermediate Filament Proteins - biosynthesis laser Lasers, Semiconductor - adverse effects Molar Nerve Tissue Proteins - biosynthesis Nestin odontoblasts Odontoblasts - physiology Rats Rats, Wistar Wound Healing |
title | GaAlAs Laser Irradiation Induces Active Tertiary Dentin Formation after Pulpal Apoptosis and Cell Proliferation in Rat Molars |
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