Effect of CD146+ SHED on bone regeneration in a mouse calvaria defect model

Objective Stem cells from human exfoliated deciduous teeth (SHED) have bone regeneration ability and potential therapeutic applications. CD146, a cell adhesion protein expressed by vascular endothelial cells, is involved in osteoblastic differentiation of stem cells. The effect of CD146 on SHED‐medi...

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Veröffentlicht in:Oral diseases 2023-03, Vol.29 (2), p.725-734
Hauptverfasser: Rikitake, Kodai, Kunimatsu, Ryo, Yoshimi, Yuki, Nakajima, Kengo, Hiraki, Tomoka, Aisyah Rizky Putranti, Nurul, Tsuka, Yuji, Abe, Takaharu, Ando, Kazuyo, Hayashi, Yoko, Nikawa, Hiroki, Tanimoto, Kotaro
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container_end_page 734
container_issue 2
container_start_page 725
container_title Oral diseases
container_volume 29
creator Rikitake, Kodai
Kunimatsu, Ryo
Yoshimi, Yuki
Nakajima, Kengo
Hiraki, Tomoka
Aisyah Rizky Putranti, Nurul
Tsuka, Yuji
Abe, Takaharu
Ando, Kazuyo
Hayashi, Yoko
Nikawa, Hiroki
Tanimoto, Kotaro
description Objective Stem cells from human exfoliated deciduous teeth (SHED) have bone regeneration ability and potential therapeutic applications. CD146, a cell adhesion protein expressed by vascular endothelial cells, is involved in osteoblastic differentiation of stem cells. The effect of CD146 on SHED‐mediated bone regeneration in vivo remains unknown. We aimed to establish efficient conditions for SHED transplantation. Materials and methods SHED were isolated from the pulp of an extracted deciduous tooth and cultured; CD146‐positive (CD146+) and CD146‐negative (CD146−) populations were sorted. Heterogeneous populations of SHED and CD146+ and CD146− cells were transplanted into bone defects generated in the skulls of immunodeficient mice. Micro‐computed tomography was performed immediately and 4 and 8 weeks later. Histological and immunohistochemical assessments were performed 8 weeks later. Results Bone regeneration was observed upon transplantation with CD146+ and heterogeneous populations of SHED, with significantly higher bone regeneration observed with CD146+ cells. Bone regeneration was higher in the CD146− group than in the control group, but significantly lower than that in the other transplant groups at 4 and 8 weeks. Histological and immunohistochemical assessments revealed that CD146+ cells promoted bone regeneration and angiogenesis. Conclusion Transplantation of CD146+ SHED into bone defects may be useful for bone regeneration.
doi_str_mv 10.1111/odi.14020
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CD146, a cell adhesion protein expressed by vascular endothelial cells, is involved in osteoblastic differentiation of stem cells. The effect of CD146 on SHED‐mediated bone regeneration in vivo remains unknown. We aimed to establish efficient conditions for SHED transplantation. Materials and methods SHED were isolated from the pulp of an extracted deciduous tooth and cultured; CD146‐positive (CD146+) and CD146‐negative (CD146−) populations were sorted. Heterogeneous populations of SHED and CD146+ and CD146− cells were transplanted into bone defects generated in the skulls of immunodeficient mice. Micro‐computed tomography was performed immediately and 4 and 8 weeks later. Histological and immunohistochemical assessments were performed 8 weeks later. Results Bone regeneration was observed upon transplantation with CD146+ and heterogeneous populations of SHED, with significantly higher bone regeneration observed with CD146+ cells. Bone regeneration was higher in the CD146− group than in the control group, but significantly lower than that in the other transplant groups at 4 and 8 weeks. Histological and immunohistochemical assessments revealed that CD146+ cells promoted bone regeneration and angiogenesis. Conclusion Transplantation of CD146+ SHED into bone defects may be useful for bone regeneration.</description><identifier>ISSN: 1354-523X</identifier><identifier>EISSN: 1601-0825</identifier><identifier>DOI: 10.1111/odi.14020</identifier><identifier>PMID: 34510661</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>Angiogenesis ; Animals ; Bone growth ; Bone Regeneration ; Calvaria ; CD146 ; CD146 Antigen ; Cell adhesion ; Cell Differentiation ; Computed tomography ; Dental Pulp ; Endothelial Cells ; Humans ; Immunodeficiency ; Mice ; Osteoblastogenesis ; Regeneration ; Skull - surgery ; Stem cell transplantation ; Stem cells ; stem cells from human exfoliated deciduous teeth ; Therapeutic applications ; Tooth, Deciduous ; Transplants &amp; implants ; X-Ray Microtomography</subject><ispartof>Oral diseases, 2023-03, Vol.29 (2), p.725-734</ispartof><rights>2021 Wiley Periodicals LLC</rights><rights>2021 Wiley Periodicals LLC.</rights><rights>2023 Wiley Periodicals LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4190-49de47f98ef4a9e8cd9f038a3a3083918e1d8461c0c4a3e9305f348bf9d102743</citedby><cites>FETCH-LOGICAL-c4190-49de47f98ef4a9e8cd9f038a3a3083918e1d8461c0c4a3e9305f348bf9d102743</cites><orcidid>0000-0002-5016-4957</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fodi.14020$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fodi.14020$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34510661$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rikitake, Kodai</creatorcontrib><creatorcontrib>Kunimatsu, Ryo</creatorcontrib><creatorcontrib>Yoshimi, Yuki</creatorcontrib><creatorcontrib>Nakajima, Kengo</creatorcontrib><creatorcontrib>Hiraki, Tomoka</creatorcontrib><creatorcontrib>Aisyah Rizky Putranti, Nurul</creatorcontrib><creatorcontrib>Tsuka, Yuji</creatorcontrib><creatorcontrib>Abe, Takaharu</creatorcontrib><creatorcontrib>Ando, Kazuyo</creatorcontrib><creatorcontrib>Hayashi, Yoko</creatorcontrib><creatorcontrib>Nikawa, Hiroki</creatorcontrib><creatorcontrib>Tanimoto, Kotaro</creatorcontrib><title>Effect of CD146+ SHED on bone regeneration in a mouse calvaria defect model</title><title>Oral diseases</title><addtitle>Oral Dis</addtitle><description>Objective Stem cells from human exfoliated deciduous teeth (SHED) have bone regeneration ability and potential therapeutic applications. CD146, a cell adhesion protein expressed by vascular endothelial cells, is involved in osteoblastic differentiation of stem cells. The effect of CD146 on SHED‐mediated bone regeneration in vivo remains unknown. We aimed to establish efficient conditions for SHED transplantation. Materials and methods SHED were isolated from the pulp of an extracted deciduous tooth and cultured; CD146‐positive (CD146+) and CD146‐negative (CD146−) populations were sorted. Heterogeneous populations of SHED and CD146+ and CD146− cells were transplanted into bone defects generated in the skulls of immunodeficient mice. Micro‐computed tomography was performed immediately and 4 and 8 weeks later. Histological and immunohistochemical assessments were performed 8 weeks later. Results Bone regeneration was observed upon transplantation with CD146+ and heterogeneous populations of SHED, with significantly higher bone regeneration observed with CD146+ cells. Bone regeneration was higher in the CD146− group than in the control group, but significantly lower than that in the other transplant groups at 4 and 8 weeks. Histological and immunohistochemical assessments revealed that CD146+ cells promoted bone regeneration and angiogenesis. Conclusion Transplantation of CD146+ SHED into bone defects may be useful for bone regeneration.</description><subject>Angiogenesis</subject><subject>Animals</subject><subject>Bone growth</subject><subject>Bone Regeneration</subject><subject>Calvaria</subject><subject>CD146</subject><subject>CD146 Antigen</subject><subject>Cell adhesion</subject><subject>Cell Differentiation</subject><subject>Computed tomography</subject><subject>Dental Pulp</subject><subject>Endothelial Cells</subject><subject>Humans</subject><subject>Immunodeficiency</subject><subject>Mice</subject><subject>Osteoblastogenesis</subject><subject>Regeneration</subject><subject>Skull - surgery</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>stem cells from human exfoliated deciduous teeth</subject><subject>Therapeutic applications</subject><subject>Tooth, Deciduous</subject><subject>Transplants &amp; implants</subject><subject>X-Ray Microtomography</subject><issn>1354-523X</issn><issn>1601-0825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1LxDAQhoMofqwe_AMS8KJIdycfbZOj7K4fKHhQwVvIthOptI2mW2X_vXGrHgTnMsPwzMPwEnLIYMxiTXxZjZkEDhtkl2XAElA83YyzSGWScvG0Q_a67gWA5VrwbbIjZMogy9guuZk7h8WSekenMyazM3p_NZ9R39KFb5EGfMYWg11WcVO11NLG9x3SwtbvNlSWlrg-b3yJ9T7Zcrbu8OC7j8jjxfxhepXc3l1eT89vk0IyDYnUJcrcaYVOWo2qKLUDoaywApTQTCErlcxYAYW0ArWA1AmpFk6XDHguxYicDN7X4N967JamqboC69q2GL8zPM05F5BDGtHjP-iL70MbvzM8zznLFIc8UqcDVQTfdQGdeQ1VY8PKMDBfCZuYsFknHNmjb2O_aLD8JX8ijcBkAD6qGlf_m8zd7HpQfgKox4DC</recordid><startdate>202303</startdate><enddate>202303</enddate><creator>Rikitake, Kodai</creator><creator>Kunimatsu, Ryo</creator><creator>Yoshimi, Yuki</creator><creator>Nakajima, Kengo</creator><creator>Hiraki, Tomoka</creator><creator>Aisyah Rizky Putranti, Nurul</creator><creator>Tsuka, Yuji</creator><creator>Abe, Takaharu</creator><creator>Ando, Kazuyo</creator><creator>Hayashi, Yoko</creator><creator>Nikawa, Hiroki</creator><creator>Tanimoto, Kotaro</creator><general>Wiley Subscription Services, 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>7QP</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5016-4957</orcidid></search><sort><creationdate>202303</creationdate><title>Effect of CD146+ SHED on bone regeneration in a mouse calvaria defect model</title><author>Rikitake, Kodai ; Kunimatsu, Ryo ; Yoshimi, Yuki ; Nakajima, Kengo ; Hiraki, Tomoka ; Aisyah Rizky Putranti, Nurul ; Tsuka, Yuji ; Abe, Takaharu ; Ando, Kazuyo ; Hayashi, Yoko ; Nikawa, Hiroki ; Tanimoto, Kotaro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4190-49de47f98ef4a9e8cd9f038a3a3083918e1d8461c0c4a3e9305f348bf9d102743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Angiogenesis</topic><topic>Animals</topic><topic>Bone growth</topic><topic>Bone Regeneration</topic><topic>Calvaria</topic><topic>CD146</topic><topic>CD146 Antigen</topic><topic>Cell adhesion</topic><topic>Cell Differentiation</topic><topic>Computed tomography</topic><topic>Dental Pulp</topic><topic>Endothelial Cells</topic><topic>Humans</topic><topic>Immunodeficiency</topic><topic>Mice</topic><topic>Osteoblastogenesis</topic><topic>Regeneration</topic><topic>Skull - surgery</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><topic>stem cells from human exfoliated deciduous teeth</topic><topic>Therapeutic applications</topic><topic>Tooth, Deciduous</topic><topic>Transplants &amp; implants</topic><topic>X-Ray Microtomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rikitake, Kodai</creatorcontrib><creatorcontrib>Kunimatsu, Ryo</creatorcontrib><creatorcontrib>Yoshimi, Yuki</creatorcontrib><creatorcontrib>Nakajima, Kengo</creatorcontrib><creatorcontrib>Hiraki, Tomoka</creatorcontrib><creatorcontrib>Aisyah Rizky Putranti, Nurul</creatorcontrib><creatorcontrib>Tsuka, Yuji</creatorcontrib><creatorcontrib>Abe, Takaharu</creatorcontrib><creatorcontrib>Ando, Kazuyo</creatorcontrib><creatorcontrib>Hayashi, Yoko</creatorcontrib><creatorcontrib>Nikawa, Hiroki</creatorcontrib><creatorcontrib>Tanimoto, Kotaro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Oral diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rikitake, Kodai</au><au>Kunimatsu, Ryo</au><au>Yoshimi, Yuki</au><au>Nakajima, Kengo</au><au>Hiraki, Tomoka</au><au>Aisyah Rizky Putranti, Nurul</au><au>Tsuka, Yuji</au><au>Abe, Takaharu</au><au>Ando, Kazuyo</au><au>Hayashi, Yoko</au><au>Nikawa, Hiroki</au><au>Tanimoto, Kotaro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of CD146+ SHED on bone regeneration in a mouse calvaria defect model</atitle><jtitle>Oral diseases</jtitle><addtitle>Oral Dis</addtitle><date>2023-03</date><risdate>2023</risdate><volume>29</volume><issue>2</issue><spage>725</spage><epage>734</epage><pages>725-734</pages><issn>1354-523X</issn><eissn>1601-0825</eissn><abstract>Objective Stem cells from human exfoliated deciduous teeth (SHED) have bone regeneration ability and potential therapeutic applications. CD146, a cell adhesion protein expressed by vascular endothelial cells, is involved in osteoblastic differentiation of stem cells. The effect of CD146 on SHED‐mediated bone regeneration in vivo remains unknown. We aimed to establish efficient conditions for SHED transplantation. Materials and methods SHED were isolated from the pulp of an extracted deciduous tooth and cultured; CD146‐positive (CD146+) and CD146‐negative (CD146−) populations were sorted. Heterogeneous populations of SHED and CD146+ and CD146− cells were transplanted into bone defects generated in the skulls of immunodeficient mice. Micro‐computed tomography was performed immediately and 4 and 8 weeks later. Histological and immunohistochemical assessments were performed 8 weeks later. Results Bone regeneration was observed upon transplantation with CD146+ and heterogeneous populations of SHED, with significantly higher bone regeneration observed with CD146+ cells. Bone regeneration was higher in the CD146− group than in the control group, but significantly lower than that in the other transplant groups at 4 and 8 weeks. Histological and immunohistochemical assessments revealed that CD146+ cells promoted bone regeneration and angiogenesis. Conclusion Transplantation of CD146+ SHED into bone defects may be useful for bone regeneration.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34510661</pmid><doi>10.1111/odi.14020</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-5016-4957</orcidid></addata></record>
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subjects Angiogenesis
Animals
Bone growth
Bone Regeneration
Calvaria
CD146
CD146 Antigen
Cell adhesion
Cell Differentiation
Computed tomography
Dental Pulp
Endothelial Cells
Humans
Immunodeficiency
Mice
Osteoblastogenesis
Regeneration
Skull - surgery
Stem cell transplantation
Stem cells
stem cells from human exfoliated deciduous teeth
Therapeutic applications
Tooth, Deciduous
Transplants & implants
X-Ray Microtomography
title Effect of CD146+ SHED on bone regeneration in a mouse calvaria defect model
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