Morphology of the Myocardium after Experimental Bone Tissue Trauma and the Use of Extracellular Vesicles Derived from Mesenchymal Multipotent Stromal Cells

The effect of extracellular vesicles (EVs) of various origins on the heart structures in the time of health and disease has been well studied. At the same time, data on the distribution of EVs throughout the body after introduction into the tissues and the possibility of the influence of these EVs o...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of personalized medicine 2021-11, Vol.11 (11), p.1206, Article 1206
Hauptverfasser: Maiborodin, Igor, Klinnikova, Marina, Kuzkin, Sergey, Maiborodina, Vitalina, Krasil'nikov, Sergey, Pichigina, Aleksandra, Lushnikova, Elena
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 11
container_start_page 1206
container_title Journal of personalized medicine
container_volume 11
creator Maiborodin, Igor
Klinnikova, Marina
Kuzkin, Sergey
Maiborodina, Vitalina
Krasil'nikov, Sergey
Pichigina, Aleksandra
Lushnikova, Elena
description The effect of extracellular vesicles (EVs) of various origins on the heart structures in the time of health and disease has been well studied. At the same time, data on the distribution of EVs throughout the body after introduction into the tissues and the possibility of the influence of these EVs on organs distant from the injection site are practically absent. It is also necessary to note a certain inconsistency in the results of various researchers: from articles on the direct absorption of EVs derived from mesenchymal multipotent stromal cells (MSC EVs) by cardiomyocytes to the data that the heart is inherently immune to drug delivery mediated by nanoparticles. In this regard, the morphological changes in the myocardium of outbred rabbits of both sexes weighing 3-4 kg were studied at various times after experimental trauma of the bone tissue in the proximal condyle of the tibia (PCT) and the use of MSC EVs. As a result of modeling the PCT defect, rabbits develop myocardial edema in the heart muscle by the 3rd day, their lymphatic vessels expand, and then, on the 7th day, the blood vessels become dilated. In the myocardium, the relative and absolute contents of neutrophils, erythrocytes, and macrophages increase, but the percentage of lymphocytes decreases. By day 10, almost all of these changes return to their initial values. The detected transformations of the myocardium are most likely due to the ingress of detritus with the blood flow from the PCT. The use of MSC EVs to influence the regeneration of damaged tissue of PCT promotes earlier dilatation of the blood vessels of the heart with pronounced diapedesis of erythrocytes or even hemorrhages, prolongation of edema, the formation of blood clots in vessels with obliteration of their lumen, sclerotic transformation of vascular walls and paravascular tissues. In the myocardium, the number density of neutrophils, the percentage of lymphocytes, and neutrophils become smaller, with a simultaneous increase in the relative numbers of erythrocytes and macrophages, and changes in the content of macrophages remained until the end of the observation-up to 10 days after the surgery. The discovered effect of MSC EVs is most likely associated with the suppression of the activity of the inflammatory process in the PCT area, which, in turn, was caused by a longer ingress of detritus with blood flow into the myocardium. The absence of statistically significant differences between changes in the myocardium of the lef
doi_str_mv 10.3390/jpm11111206
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_3390_jpm11111206</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2602094790</sourcerecordid><originalsourceid>FETCH-LOGICAL-c386t-256d1685d0f9379a99eb51a30bee4f9eed5dba10fc1b6cfaef5e95a10606aafd3</originalsourceid><addsrcrecordid>eNqNUk1v1DAQjRCIVqUn_oAlLkhoi53ETnxBgnQLSF1xoOUaTZxx16skDv4o3d_Cn8Vhq1I44ctYM-89z8xzlr1k9KwoJH27m0e2nJyKJ9lxTiu-KstcPH10P8pOvd_RdGqe54I-z46Ksi5Kzuvj7OfGunlrB3uzJ1aTsEWy2VsFrjdxJKADOrK-m9GZEacAA_lgJyRXxvuYgoM4AoGp_0289rhorO-CA4XDEAdw5Bt6owb05Dxp3GJPtLMj2aDHSW33Y1LcxCGY2YakT76GVE25JtH9i-yZhsHj6X08ya4v1lfNp9Xll4-fm_eXK1XUIqxyLnomat5TLYtKgpTYcQYF7RBLLRF73nfAqFasE0oDao6Sp4SgAkD3xUn27qA7x27EXqVGHAztnGYGt28tmPbvymS27Y29bWuRs4qVSeD1vYCz3yP60I7GLxuACW30bVp6SRml1QJ99Q90Z6Ob0ngLKqeyrCRNqDcHlHLWe4f6oRlG28X39pHvCV0f0D-ws9ork1aLD4zke5Un45lcvgBrTIBg7NTYOIU_D_0PtfgFjxfDtA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2602094790</pqid></control><display><type>article</type><title>Morphology of the Myocardium after Experimental Bone Tissue Trauma and the Use of Extracellular Vesicles Derived from Mesenchymal Multipotent Stromal Cells</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central Open Access</source><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>Web of Science - Science Citation Index Expanded - 2021&lt;img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" /&gt;</source><source>PubMed Central</source><creator>Maiborodin, Igor ; Klinnikova, Marina ; Kuzkin, Sergey ; Maiborodina, Vitalina ; Krasil'nikov, Sergey ; Pichigina, Aleksandra ; Lushnikova, Elena</creator><creatorcontrib>Maiborodin, Igor ; Klinnikova, Marina ; Kuzkin, Sergey ; Maiborodina, Vitalina ; Krasil'nikov, Sergey ; Pichigina, Aleksandra ; Lushnikova, Elena</creatorcontrib><description>The effect of extracellular vesicles (EVs) of various origins on the heart structures in the time of health and disease has been well studied. At the same time, data on the distribution of EVs throughout the body after introduction into the tissues and the possibility of the influence of these EVs on organs distant from the injection site are practically absent. It is also necessary to note a certain inconsistency in the results of various researchers: from articles on the direct absorption of EVs derived from mesenchymal multipotent stromal cells (MSC EVs) by cardiomyocytes to the data that the heart is inherently immune to drug delivery mediated by nanoparticles. In this regard, the morphological changes in the myocardium of outbred rabbits of both sexes weighing 3-4 kg were studied at various times after experimental trauma of the bone tissue in the proximal condyle of the tibia (PCT) and the use of MSC EVs. As a result of modeling the PCT defect, rabbits develop myocardial edema in the heart muscle by the 3rd day, their lymphatic vessels expand, and then, on the 7th day, the blood vessels become dilated. In the myocardium, the relative and absolute contents of neutrophils, erythrocytes, and macrophages increase, but the percentage of lymphocytes decreases. By day 10, almost all of these changes return to their initial values. The detected transformations of the myocardium are most likely due to the ingress of detritus with the blood flow from the PCT. The use of MSC EVs to influence the regeneration of damaged tissue of PCT promotes earlier dilatation of the blood vessels of the heart with pronounced diapedesis of erythrocytes or even hemorrhages, prolongation of edema, the formation of blood clots in vessels with obliteration of their lumen, sclerotic transformation of vascular walls and paravascular tissues. In the myocardium, the number density of neutrophils, the percentage of lymphocytes, and neutrophils become smaller, with a simultaneous increase in the relative numbers of erythrocytes and macrophages, and changes in the content of macrophages remained until the end of the observation-up to 10 days after the surgery. The discovered effect of MSC EVs is most likely associated with the suppression of the activity of the inflammatory process in the PCT area, which, in turn, was caused by a longer ingress of detritus with blood flow into the myocardium. The absence of statistically significant differences between changes in the myocardium of the left and right ventricles may indicate that both detritus from the surgical site and MSC EVs affect the heart spreading through the coronary artery system.</description><identifier>ISSN: 2075-4426</identifier><identifier>EISSN: 2075-4426</identifier><identifier>DOI: 10.3390/jpm11111206</identifier><identifier>PMID: 34834558</identifier><language>eng</language><publisher>BASEL: Mdpi</publisher><subject>Blood coagulation ; Blood flow ; Blood vessels ; Bone marrow ; Cardiac muscle ; Cardiomyocytes ; Communication ; Coronary artery ; Detritus ; Diapedesis ; Drug delivery ; Drug dosages ; Edema ; Erythrocytes ; Extracellular vesicles ; General &amp; Internal Medicine ; Health Care Sciences &amp; Services ; Inflammation ; Laboratory animals ; Leukocytes (neutrophilic) ; Life Sciences &amp; Biomedicine ; Lymphatic system ; Lymphocytes ; Macrophages ; Medical research ; Medicine, General &amp; Internal ; Mesenchyme ; MicroRNAs ; Morphology ; Myocardium ; Nanoparticles ; Precision medicine ; Regeneration ; Research methodology ; Science &amp; Technology ; Software ; State budgets ; Statistical analysis ; Stromal cells ; Tibia ; Trauma ; Umbilical cord</subject><ispartof>Journal of personalized medicine, 2021-11, Vol.11 (11), p.1206, Article 1206</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>2</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000725221900001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c386t-256d1685d0f9379a99eb51a30bee4f9eed5dba10fc1b6cfaef5e95a10606aafd3</citedby><cites>FETCH-LOGICAL-c386t-256d1685d0f9379a99eb51a30bee4f9eed5dba10fc1b6cfaef5e95a10606aafd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621714/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621714/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,887,27931,27932,39265,53798,53800</link.rule.ids></links><search><creatorcontrib>Maiborodin, Igor</creatorcontrib><creatorcontrib>Klinnikova, Marina</creatorcontrib><creatorcontrib>Kuzkin, Sergey</creatorcontrib><creatorcontrib>Maiborodina, Vitalina</creatorcontrib><creatorcontrib>Krasil'nikov, Sergey</creatorcontrib><creatorcontrib>Pichigina, Aleksandra</creatorcontrib><creatorcontrib>Lushnikova, Elena</creatorcontrib><title>Morphology of the Myocardium after Experimental Bone Tissue Trauma and the Use of Extracellular Vesicles Derived from Mesenchymal Multipotent Stromal Cells</title><title>Journal of personalized medicine</title><addtitle>J PERS MED</addtitle><description>The effect of extracellular vesicles (EVs) of various origins on the heart structures in the time of health and disease has been well studied. At the same time, data on the distribution of EVs throughout the body after introduction into the tissues and the possibility of the influence of these EVs on organs distant from the injection site are practically absent. It is also necessary to note a certain inconsistency in the results of various researchers: from articles on the direct absorption of EVs derived from mesenchymal multipotent stromal cells (MSC EVs) by cardiomyocytes to the data that the heart is inherently immune to drug delivery mediated by nanoparticles. In this regard, the morphological changes in the myocardium of outbred rabbits of both sexes weighing 3-4 kg were studied at various times after experimental trauma of the bone tissue in the proximal condyle of the tibia (PCT) and the use of MSC EVs. As a result of modeling the PCT defect, rabbits develop myocardial edema in the heart muscle by the 3rd day, their lymphatic vessels expand, and then, on the 7th day, the blood vessels become dilated. In the myocardium, the relative and absolute contents of neutrophils, erythrocytes, and macrophages increase, but the percentage of lymphocytes decreases. By day 10, almost all of these changes return to their initial values. The detected transformations of the myocardium are most likely due to the ingress of detritus with the blood flow from the PCT. The use of MSC EVs to influence the regeneration of damaged tissue of PCT promotes earlier dilatation of the blood vessels of the heart with pronounced diapedesis of erythrocytes or even hemorrhages, prolongation of edema, the formation of blood clots in vessels with obliteration of their lumen, sclerotic transformation of vascular walls and paravascular tissues. In the myocardium, the number density of neutrophils, the percentage of lymphocytes, and neutrophils become smaller, with a simultaneous increase in the relative numbers of erythrocytes and macrophages, and changes in the content of macrophages remained until the end of the observation-up to 10 days after the surgery. The discovered effect of MSC EVs is most likely associated with the suppression of the activity of the inflammatory process in the PCT area, which, in turn, was caused by a longer ingress of detritus with blood flow into the myocardium. The absence of statistically significant differences between changes in the myocardium of the left and right ventricles may indicate that both detritus from the surgical site and MSC EVs affect the heart spreading through the coronary artery system.</description><subject>Blood coagulation</subject><subject>Blood flow</subject><subject>Blood vessels</subject><subject>Bone marrow</subject><subject>Cardiac muscle</subject><subject>Cardiomyocytes</subject><subject>Communication</subject><subject>Coronary artery</subject><subject>Detritus</subject><subject>Diapedesis</subject><subject>Drug delivery</subject><subject>Drug dosages</subject><subject>Edema</subject><subject>Erythrocytes</subject><subject>Extracellular vesicles</subject><subject>General &amp; Internal Medicine</subject><subject>Health Care Sciences &amp; Services</subject><subject>Inflammation</subject><subject>Laboratory animals</subject><subject>Leukocytes (neutrophilic)</subject><subject>Life Sciences &amp; Biomedicine</subject><subject>Lymphatic system</subject><subject>Lymphocytes</subject><subject>Macrophages</subject><subject>Medical research</subject><subject>Medicine, General &amp; Internal</subject><subject>Mesenchyme</subject><subject>MicroRNAs</subject><subject>Morphology</subject><subject>Myocardium</subject><subject>Nanoparticles</subject><subject>Precision medicine</subject><subject>Regeneration</subject><subject>Research methodology</subject><subject>Science &amp; Technology</subject><subject>Software</subject><subject>State budgets</subject><subject>Statistical analysis</subject><subject>Stromal cells</subject><subject>Tibia</subject><subject>Trauma</subject><subject>Umbilical cord</subject><issn>2075-4426</issn><issn>2075-4426</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNUk1v1DAQjRCIVqUn_oAlLkhoi53ETnxBgnQLSF1xoOUaTZxx16skDv4o3d_Cn8Vhq1I44ctYM-89z8xzlr1k9KwoJH27m0e2nJyKJ9lxTiu-KstcPH10P8pOvd_RdGqe54I-z46Ksi5Kzuvj7OfGunlrB3uzJ1aTsEWy2VsFrjdxJKADOrK-m9GZEacAA_lgJyRXxvuYgoM4AoGp_0289rhorO-CA4XDEAdw5Bt6owb05Dxp3GJPtLMj2aDHSW33Y1LcxCGY2YakT76GVE25JtH9i-yZhsHj6X08ya4v1lfNp9Xll4-fm_eXK1XUIqxyLnomat5TLYtKgpTYcQYF7RBLLRF73nfAqFasE0oDao6Sp4SgAkD3xUn27qA7x27EXqVGHAztnGYGt28tmPbvymS27Y29bWuRs4qVSeD1vYCz3yP60I7GLxuACW30bVp6SRml1QJ99Q90Z6Ob0ngLKqeyrCRNqDcHlHLWe4f6oRlG28X39pHvCV0f0D-ws9ork1aLD4zke5Un45lcvgBrTIBg7NTYOIU_D_0PtfgFjxfDtA</recordid><startdate>20211115</startdate><enddate>20211115</enddate><creator>Maiborodin, Igor</creator><creator>Klinnikova, Marina</creator><creator>Kuzkin, Sergey</creator><creator>Maiborodina, Vitalina</creator><creator>Krasil'nikov, Sergey</creator><creator>Pichigina, Aleksandra</creator><creator>Lushnikova, Elena</creator><general>Mdpi</general><general>MDPI AG</general><general>MDPI</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20211115</creationdate><title>Morphology of the Myocardium after Experimental Bone Tissue Trauma and the Use of Extracellular Vesicles Derived from Mesenchymal Multipotent Stromal Cells</title><author>Maiborodin, Igor ; Klinnikova, Marina ; Kuzkin, Sergey ; Maiborodina, Vitalina ; Krasil'nikov, Sergey ; Pichigina, Aleksandra ; Lushnikova, Elena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-256d1685d0f9379a99eb51a30bee4f9eed5dba10fc1b6cfaef5e95a10606aafd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Blood coagulation</topic><topic>Blood flow</topic><topic>Blood vessels</topic><topic>Bone marrow</topic><topic>Cardiac muscle</topic><topic>Cardiomyocytes</topic><topic>Communication</topic><topic>Coronary artery</topic><topic>Detritus</topic><topic>Diapedesis</topic><topic>Drug delivery</topic><topic>Drug dosages</topic><topic>Edema</topic><topic>Erythrocytes</topic><topic>Extracellular vesicles</topic><topic>General &amp; Internal Medicine</topic><topic>Health Care Sciences &amp; Services</topic><topic>Inflammation</topic><topic>Laboratory animals</topic><topic>Leukocytes (neutrophilic)</topic><topic>Life Sciences &amp; Biomedicine</topic><topic>Lymphatic system</topic><topic>Lymphocytes</topic><topic>Macrophages</topic><topic>Medical research</topic><topic>Medicine, General &amp; Internal</topic><topic>Mesenchyme</topic><topic>MicroRNAs</topic><topic>Morphology</topic><topic>Myocardium</topic><topic>Nanoparticles</topic><topic>Precision medicine</topic><topic>Regeneration</topic><topic>Research methodology</topic><topic>Science &amp; Technology</topic><topic>Software</topic><topic>State budgets</topic><topic>Statistical analysis</topic><topic>Stromal cells</topic><topic>Tibia</topic><topic>Trauma</topic><topic>Umbilical cord</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maiborodin, Igor</creatorcontrib><creatorcontrib>Klinnikova, Marina</creatorcontrib><creatorcontrib>Kuzkin, Sergey</creatorcontrib><creatorcontrib>Maiborodina, Vitalina</creatorcontrib><creatorcontrib>Krasil'nikov, Sergey</creatorcontrib><creatorcontrib>Pichigina, Aleksandra</creatorcontrib><creatorcontrib>Lushnikova, Elena</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of personalized medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maiborodin, Igor</au><au>Klinnikova, Marina</au><au>Kuzkin, Sergey</au><au>Maiborodina, Vitalina</au><au>Krasil'nikov, Sergey</au><au>Pichigina, Aleksandra</au><au>Lushnikova, Elena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morphology of the Myocardium after Experimental Bone Tissue Trauma and the Use of Extracellular Vesicles Derived from Mesenchymal Multipotent Stromal Cells</atitle><jtitle>Journal of personalized medicine</jtitle><stitle>J PERS MED</stitle><date>2021-11-15</date><risdate>2021</risdate><volume>11</volume><issue>11</issue><spage>1206</spage><pages>1206-</pages><artnum>1206</artnum><issn>2075-4426</issn><eissn>2075-4426</eissn><abstract>The effect of extracellular vesicles (EVs) of various origins on the heart structures in the time of health and disease has been well studied. At the same time, data on the distribution of EVs throughout the body after introduction into the tissues and the possibility of the influence of these EVs on organs distant from the injection site are practically absent. It is also necessary to note a certain inconsistency in the results of various researchers: from articles on the direct absorption of EVs derived from mesenchymal multipotent stromal cells (MSC EVs) by cardiomyocytes to the data that the heart is inherently immune to drug delivery mediated by nanoparticles. In this regard, the morphological changes in the myocardium of outbred rabbits of both sexes weighing 3-4 kg were studied at various times after experimental trauma of the bone tissue in the proximal condyle of the tibia (PCT) and the use of MSC EVs. As a result of modeling the PCT defect, rabbits develop myocardial edema in the heart muscle by the 3rd day, their lymphatic vessels expand, and then, on the 7th day, the blood vessels become dilated. In the myocardium, the relative and absolute contents of neutrophils, erythrocytes, and macrophages increase, but the percentage of lymphocytes decreases. By day 10, almost all of these changes return to their initial values. The detected transformations of the myocardium are most likely due to the ingress of detritus with the blood flow from the PCT. The use of MSC EVs to influence the regeneration of damaged tissue of PCT promotes earlier dilatation of the blood vessels of the heart with pronounced diapedesis of erythrocytes or even hemorrhages, prolongation of edema, the formation of blood clots in vessels with obliteration of their lumen, sclerotic transformation of vascular walls and paravascular tissues. In the myocardium, the number density of neutrophils, the percentage of lymphocytes, and neutrophils become smaller, with a simultaneous increase in the relative numbers of erythrocytes and macrophages, and changes in the content of macrophages remained until the end of the observation-up to 10 days after the surgery. The discovered effect of MSC EVs is most likely associated with the suppression of the activity of the inflammatory process in the PCT area, which, in turn, was caused by a longer ingress of detritus with blood flow into the myocardium. The absence of statistically significant differences between changes in the myocardium of the left and right ventricles may indicate that both detritus from the surgical site and MSC EVs affect the heart spreading through the coronary artery system.</abstract><cop>BASEL</cop><pub>Mdpi</pub><pmid>34834558</pmid><doi>10.3390/jpm11111206</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2075-4426
ispartof Journal of personalized medicine, 2021-11, Vol.11 (11), p.1206, Article 1206
issn 2075-4426
2075-4426
language eng
recordid cdi_crossref_primary_10_3390_jpm11111206
source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; MDPI - Multidisciplinary Digital Publishing Institute; Web of Science - Science Citation Index Expanded - 2021<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" />; PubMed Central
subjects Blood coagulation
Blood flow
Blood vessels
Bone marrow
Cardiac muscle
Cardiomyocytes
Communication
Coronary artery
Detritus
Diapedesis
Drug delivery
Drug dosages
Edema
Erythrocytes
Extracellular vesicles
General & Internal Medicine
Health Care Sciences & Services
Inflammation
Laboratory animals
Leukocytes (neutrophilic)
Life Sciences & Biomedicine
Lymphatic system
Lymphocytes
Macrophages
Medical research
Medicine, General & Internal
Mesenchyme
MicroRNAs
Morphology
Myocardium
Nanoparticles
Precision medicine
Regeneration
Research methodology
Science & Technology
Software
State budgets
Statistical analysis
Stromal cells
Tibia
Trauma
Umbilical cord
title Morphology of the Myocardium after Experimental Bone Tissue Trauma and the Use of Extracellular Vesicles Derived from Mesenchymal Multipotent Stromal Cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-05T02%3A43%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Morphology%20of%20the%20Myocardium%20after%20Experimental%20Bone%20Tissue%20Trauma%20and%20the%20Use%20of%20Extracellular%20Vesicles%20Derived%20from%20Mesenchymal%20Multipotent%20Stromal%20Cells&rft.jtitle=Journal%20of%20personalized%20medicine&rft.au=Maiborodin,%20Igor&rft.date=2021-11-15&rft.volume=11&rft.issue=11&rft.spage=1206&rft.pages=1206-&rft.artnum=1206&rft.issn=2075-4426&rft.eissn=2075-4426&rft_id=info:doi/10.3390/jpm11111206&rft_dat=%3Cproquest_cross%3E2602094790%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2602094790&rft_id=info:pmid/34834558&rfr_iscdi=true