Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?
Perinatal complications in both term- and preterm-born infants are a leading cause of neonatal morbidities and mortality. Infants face different challenges in the neonatal intensive care unit with long-term morbidities such as perinatal brain injury and bronchopulmonary dysplasia being particularly...
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description | Perinatal complications in both term- and preterm-born infants are a leading cause of neonatal morbidities and mortality. Infants face different challenges in the neonatal intensive care unit with long-term morbidities such as perinatal brain injury and bronchopulmonary dysplasia being particularly devastating. While advances in perinatal medicine have improved our understanding of the pathogenesis, effective therapies to prevent and/or reduce the severity of these disorders are still lacking. The potential of mesenchymal stem/stromal cell (MSC) therapy has emerged during the last two decades, and an increasing effort is conducted to address brain- and lung-related morbidities in neonates at risk. Various studies support the notion that MSCs have protective effects. MSCs are an easy source and may be readily available after birth in a clinical setting. MSCs’ mechanisms of action are diverse, including migration and homing, release of growth factors and immunomodulation, and the potential to replace injured cells. Here, we review the pathophysiology of perinatally acquired brain and lung injuries and focus on MSCs as potential candidates for therapeutic strategies summarizing preclinical and clinical evidence. |
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A. ; Schoeberlein, Andreina ; Gavilanes, Antonio W. D. ; Surbek, Daniel ; Kramer, Boris W.</creator><creatorcontrib>Mueller, Martin ; Wolfs, Tim G. A. ; Schoeberlein, Andreina ; Gavilanes, Antonio W. D. ; Surbek, Daniel ; Kramer, Boris W.</creatorcontrib><description>Perinatal complications in both term- and preterm-born infants are a leading cause of neonatal morbidities and mortality. Infants face different challenges in the neonatal intensive care unit with long-term morbidities such as perinatal brain injury and bronchopulmonary dysplasia being particularly devastating. While advances in perinatal medicine have improved our understanding of the pathogenesis, effective therapies to prevent and/or reduce the severity of these disorders are still lacking. The potential of mesenchymal stem/stromal cell (MSC) therapy has emerged during the last two decades, and an increasing effort is conducted to address brain- and lung-related morbidities in neonates at risk. Various studies support the notion that MSCs have protective effects. MSCs are an easy source and may be readily available after birth in a clinical setting. MSCs’ mechanisms of action are diverse, including migration and homing, release of growth factors and immunomodulation, and the potential to replace injured cells. Here, we review the pathophysiology of perinatally acquired brain and lung injuries and focus on MSCs as potential candidates for therapeutic strategies summarizing preclinical and clinical evidence.</description><identifier>ISSN: 2194-7791</identifier><identifier>EISSN: 2194-7791</identifier><identifier>DOI: 10.1186/s40348-016-0034-x</identifier><identifier>PMID: 26869264</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Brain damage ; Brain injury ; Diabetes ; Dysplasia ; Endocrinology ; Growth factors ; Homing behavior ; Immunomodulation ; Infants ; Medicine ; Medicine & Public Health ; Mesenchymal stem cells ; Mesenchyme ; Mini Review ; Morbidity ; Neonates ; Newborn babies ; Oncology ; Pediatrics ; Recent advances in pediatric lung diseases ; Regeneration ; Stromal cells</subject><ispartof>Molecular and cellular pediatrics, 2016-02, Vol.3 (1), p.6-9, Article 6</ispartof><rights>Mueller et al. 2016</rights><rights>Molecular and Cellular Pediatrics is a copyright of Springer, (2016). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315x-4e1ef363223a3cf442b3dd5486dd7d06553c018d31a98425c8a28c60f4c535993</citedby><cites>FETCH-LOGICAL-c315x-4e1ef363223a3cf442b3dd5486dd7d06553c018d31a98425c8a28c60f4c535993</cites><orcidid>0000-0001-5594-0532</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751100/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751100/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27923,27924,41119,41487,42188,42556,51318,51575,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26869264$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mueller, Martin</creatorcontrib><creatorcontrib>Wolfs, Tim G. A.</creatorcontrib><creatorcontrib>Schoeberlein, Andreina</creatorcontrib><creatorcontrib>Gavilanes, Antonio W. D.</creatorcontrib><creatorcontrib>Surbek, Daniel</creatorcontrib><creatorcontrib>Kramer, Boris W.</creatorcontrib><title>Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?</title><title>Molecular and cellular pediatrics</title><addtitle>Mol Cell Pediatr</addtitle><addtitle>Mol Cell Pediatr</addtitle><description>Perinatal complications in both term- and preterm-born infants are a leading cause of neonatal morbidities and mortality. Infants face different challenges in the neonatal intensive care unit with long-term morbidities such as perinatal brain injury and bronchopulmonary dysplasia being particularly devastating. While advances in perinatal medicine have improved our understanding of the pathogenesis, effective therapies to prevent and/or reduce the severity of these disorders are still lacking. The potential of mesenchymal stem/stromal cell (MSC) therapy has emerged during the last two decades, and an increasing effort is conducted to address brain- and lung-related morbidities in neonates at risk. Various studies support the notion that MSCs have protective effects. MSCs are an easy source and may be readily available after birth in a clinical setting. MSCs’ mechanisms of action are diverse, including migration and homing, release of growth factors and immunomodulation, and the potential to replace injured cells. Here, we review the pathophysiology of perinatally acquired brain and lung injuries and focus on MSCs as potential candidates for therapeutic strategies summarizing preclinical and clinical evidence.</description><subject>Brain damage</subject><subject>Brain injury</subject><subject>Diabetes</subject><subject>Dysplasia</subject><subject>Endocrinology</subject><subject>Growth factors</subject><subject>Homing behavior</subject><subject>Immunomodulation</subject><subject>Infants</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mesenchymal stem cells</subject><subject>Mesenchyme</subject><subject>Mini Review</subject><subject>Morbidity</subject><subject>Neonates</subject><subject>Newborn babies</subject><subject>Oncology</subject><subject>Pediatrics</subject><subject>Recent advances in pediatric lung diseases</subject><subject>Regeneration</subject><subject>Stromal cells</subject><issn>2194-7791</issn><issn>2194-7791</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kb9uFDEQxi1ERKIjD0CDVqKh2cT_125AKIKAFJQGKgrL5529OOzah-1Ddx0PkSfMk-DVhehAorA81vzmmxl_CL0g-IwQJc8zx4yrFhPZ4hq12yfohBLN267T5OlBfIxOc77FGBMhMBbdM3RMpZKaSn6Cvn2GDMHd7CY7NrnAdJ5LivPDwTjm-193tvkOu2aC3tsSUzPUk2AFAZItPobGDgVSs4bkgy21bopp6Xtfdm-fo6PBjhlOH-4F-vrh_ZeLj-3V9eWni3dXrWNEbFsOBAYmGaXMMjdwTpes7wVXsu-7HkshmMNE9YxYrTgVTlmqnMQDd4IJrdkCvdnrrjfLOqeDUJIdzTr5yaadidabvzPB35hV_Gl4Jwipn7dArx8EUvyxgVzM5PO8vw0QN9mQTlZQSDqjr_5Bb-MmhbqeIVp1mnHNukqRPeVSzDnB8DgMwWZ2z-zdM9U9M7tntrXm5eEWjxV_vKoA3QO5psIK0kHr_6r-Bvjgp3E</recordid><startdate>20160211</startdate><enddate>20160211</enddate><creator>Mueller, Martin</creator><creator>Wolfs, Tim G. 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A.</au><au>Schoeberlein, Andreina</au><au>Gavilanes, Antonio W. D.</au><au>Surbek, Daniel</au><au>Kramer, Boris W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity?</atitle><jtitle>Molecular and cellular pediatrics</jtitle><stitle>Mol Cell Pediatr</stitle><addtitle>Mol Cell Pediatr</addtitle><date>2016-02-11</date><risdate>2016</risdate><volume>3</volume><issue>1</issue><spage>6</spage><epage>9</epage><pages>6-9</pages><artnum>6</artnum><issn>2194-7791</issn><eissn>2194-7791</eissn><abstract>Perinatal complications in both term- and preterm-born infants are a leading cause of neonatal morbidities and mortality. Infants face different challenges in the neonatal intensive care unit with long-term morbidities such as perinatal brain injury and bronchopulmonary dysplasia being particularly devastating. 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subjects | Brain damage Brain injury Diabetes Dysplasia Endocrinology Growth factors Homing behavior Immunomodulation Infants Medicine Medicine & Public Health Mesenchymal stem cells Mesenchyme Mini Review Morbidity Neonates Newborn babies Oncology Pediatrics Recent advances in pediatric lung diseases Regeneration Stromal cells |
title | Mesenchymal stem/stromal cells—a key mediator for regeneration after perinatal morbidity? |
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