Intraarterial transplantation of human umbilical cord blood mononuclear cells in hyperacute stroke improves vascular function
Human umbilical cord blood (hUCB) cell therapy is a promising treatment for ischemic stroke. The effects of hyperacute stem cell transplantation on cerebrovascular function in ischemic stroke are, however, not well understood. This study evaluated the effects of hyperacute intraarterial transplantat...
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description | Human umbilical cord blood (hUCB) cell therapy is a promising treatment for ischemic stroke. The effects of hyperacute stem cell transplantation on cerebrovascular function in ischemic stroke are, however, not well understood. This study evaluated the effects of hyperacute intraarterial transplantation of hUCB mononuclear cells (MNCs) on cerebrovascular function in stroke rats using serial magnetic resonance imaging (MRI).
HUCB MNCs or vehicle were administered to stroke rats via the internal carotid artery immediately after reperfusion at 60 min following ischemia onset. Lesion volumes were longitudinally evaluated by MRI on days 0, 2, 14, and 28 after stroke, accompanied by behavioral tests. Cerebral blood flow (CBF) and cerebrovascular reactivity were measured by perfusion MRI and CO
functional MRI (fMRI) at 28 days post-stroke; corresponding vascular morphological changes were also detected by immunohistology in the same animals.
We found that CBF to the stroke-affected region at 28 days was improved (normalized CBF value: 1.41 ± 0.30 versus 0.49 ± 0.07) by intraarterial transplantation of hUCB MNCs in the hyperacute stroke phase, compared to vehicle control. Cerebrovascular reactivity within the stroke-affected area, measured by CBF fMRI, was also increased (35.2 ± 3.5% versus 12.8 ± 4.3%), as well as the corresponding cerebrovascular density. Some engrafted cells appeared with microvascular-like morphology and stained positive for von Willebrand Factor (an endothelial cell marker), suggesting they differentiated into endothelial cells. Some engrafted cells also connected to host endothelial cells, suggesting they interacted with the host vasculature. Compared to the vehicle group, infarct volume at 28 days in the stem cell treated group was significantly smaller (160.9 ± 15.7 versus 231.2 ± 16.0 mm
); behavioral deficits were also markedly reduced by stem cell treatment at day 28 (19.5 ± 1.0% versus 30.7 ± 4.7% on the foot fault test; 68.2 ± 4.6% versus 86.6 ± 5.8% on the cylinder test). More tissue within initial perfusion-diffusion mismatch was rescued in the treatment group.
Intraarterial hUCB MNC transplantation during the hyperacute phase of ischemic stroke improved cerebrovascular function and reduced behavioral deficits and infarct volume. |
doi_str_mv | 10.1186/s13287-017-0529-y |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5361847</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1885093590</sourcerecordid><originalsourceid>FETCH-LOGICAL-c493t-fe0f1269c3fa65fb05c710a9fbfc719a849b0d0066b2873d605c3fb88bdb04783</originalsourceid><addsrcrecordid>eNpdkcFqHSEYhaW0NCHNA2RThG66mVTH0dFNoYQmDQS6adaijvaaOjrV8cJd5N3rcNOQVhAP-P0HjweAC4wuMebsU8Gk52OHcNu0F93hFTjFIx07RnH_-oU-AeelPKC2CEGIDW_BSc-bpAifgsfbuGal8mqzVwE2HcsSVFzV6lOEycFdnVWEddY-eNMQk_IEdUhpgnOKKVYTrMrQ2BAK9BHuDovNytTVwrLm9MtCPy857W2Be1VMDQ12NZrN_x1441Qo9vzpPAP3119_XH3r7r7f3F59uevMIMjaOYsc7pkwxClGnUbUjBgp4bRrQig-CI2mlo3p9iVkYg0gTnOuJ42GkZMz8Pnou1Q928nYLXSQS_azygeZlJf_3kS_kz_TXlLCMB_GZvDxySCn39WWVc6-bJFVtKkWiTlHA2OCkoZ--A99SDXHFm-jKBKECtQofKRMTqVk654fg5Hc-pXHfmXrV279ykObef8yxfPE3zbJH_pYpTM</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1885093590</pqid></control><display><type>article</type><title>Intraarterial transplantation of human umbilical cord blood mononuclear cells in hyperacute stroke improves vascular function</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central Open Access</source><source>Springer Nature OA Free Journals</source><source>Springer Nature - Complete Springer Journals</source><source>PubMed Central</source><creator>Huang, Lei ; Liu, Yichu ; Lu, Jianfei ; Cerqueira, Bianca ; Misra, Vivek ; Duong, Timothy Q</creator><creatorcontrib>Huang, Lei ; Liu, Yichu ; Lu, Jianfei ; Cerqueira, Bianca ; Misra, Vivek ; Duong, Timothy Q</creatorcontrib><description>Human umbilical cord blood (hUCB) cell therapy is a promising treatment for ischemic stroke. The effects of hyperacute stem cell transplantation on cerebrovascular function in ischemic stroke are, however, not well understood. This study evaluated the effects of hyperacute intraarterial transplantation of hUCB mononuclear cells (MNCs) on cerebrovascular function in stroke rats using serial magnetic resonance imaging (MRI).
HUCB MNCs or vehicle were administered to stroke rats via the internal carotid artery immediately after reperfusion at 60 min following ischemia onset. Lesion volumes were longitudinally evaluated by MRI on days 0, 2, 14, and 28 after stroke, accompanied by behavioral tests. Cerebral blood flow (CBF) and cerebrovascular reactivity were measured by perfusion MRI and CO
functional MRI (fMRI) at 28 days post-stroke; corresponding vascular morphological changes were also detected by immunohistology in the same animals.
We found that CBF to the stroke-affected region at 28 days was improved (normalized CBF value: 1.41 ± 0.30 versus 0.49 ± 0.07) by intraarterial transplantation of hUCB MNCs in the hyperacute stroke phase, compared to vehicle control. Cerebrovascular reactivity within the stroke-affected area, measured by CBF fMRI, was also increased (35.2 ± 3.5% versus 12.8 ± 4.3%), as well as the corresponding cerebrovascular density. Some engrafted cells appeared with microvascular-like morphology and stained positive for von Willebrand Factor (an endothelial cell marker), suggesting they differentiated into endothelial cells. Some engrafted cells also connected to host endothelial cells, suggesting they interacted with the host vasculature. Compared to the vehicle group, infarct volume at 28 days in the stem cell treated group was significantly smaller (160.9 ± 15.7 versus 231.2 ± 16.0 mm
); behavioral deficits were also markedly reduced by stem cell treatment at day 28 (19.5 ± 1.0% versus 30.7 ± 4.7% on the foot fault test; 68.2 ± 4.6% versus 86.6 ± 5.8% on the cylinder test). More tissue within initial perfusion-diffusion mismatch was rescued in the treatment group.
Intraarterial hUCB MNC transplantation during the hyperacute phase of ischemic stroke improved cerebrovascular function and reduced behavioral deficits and infarct volume.</description><identifier>ISSN: 1757-6512</identifier><identifier>EISSN: 1757-6512</identifier><identifier>DOI: 10.1186/s13287-017-0529-y</identifier><identifier>PMID: 28330501</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Angiogenesis ; Animals ; Biomarkers - metabolism ; Blood flow ; Blood Flow Velocity ; Bone marrow ; Brain Ischemia - metabolism ; Brain Ischemia - pathology ; Brain Ischemia - therapy ; Carbon dioxide ; Carotid arteries ; Carotid artery ; Carotid Artery, Internal ; Cell Differentiation ; Cell Separation ; Cerebral blood flow ; Cerebrovascular Circulation ; Cerebrovascular system ; Cord blood ; Cytology ; Disease Models, Animal ; Endothelial cells ; Endothelial Cells - cytology ; Endothelial Cells - metabolism ; Experiments ; Feet ; Fetal Blood - cytology ; Fetal Blood - metabolism ; Functional magnetic resonance imaging ; Gene Expression ; Heart rate ; Humans ; Injections, Intra-Arterial ; Ischemia ; Laboratory animals ; Leukocytes (mononuclear) ; Leukocytes, Mononuclear - cytology ; Leukocytes, Mononuclear - metabolism ; Leukocytes, Mononuclear - transplantation ; Male ; Microvasculature ; NMR ; Nuclear magnetic resonance ; Perfusion ; Physiology ; Postural Balance - physiology ; Rats ; Rats, Sprague-Dawley ; Reperfusion ; Rodents ; Stem cell transplantation ; Stem cells ; Stroke ; Stroke - metabolism ; Stroke - pathology ; Stroke - therapy ; Transplantation ; Transplantation, Heterologous ; Umbilical cord ; Veins & arteries ; Von Willebrand factor ; von Willebrand Factor - genetics ; von Willebrand Factor - metabolism</subject><ispartof>Stem cell research & therapy, 2017-03, Vol.8 (1), p.74-74, Article 74</ispartof><rights>Copyright BioMed Central 2017</rights><rights>The Author(s). 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-fe0f1269c3fa65fb05c710a9fbfc719a849b0d0066b2873d605c3fb88bdb04783</citedby><cites>FETCH-LOGICAL-c493t-fe0f1269c3fa65fb05c710a9fbfc719a849b0d0066b2873d605c3fb88bdb04783</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/PMC5361847/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361847/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28330501$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Lei</creatorcontrib><creatorcontrib>Liu, Yichu</creatorcontrib><creatorcontrib>Lu, Jianfei</creatorcontrib><creatorcontrib>Cerqueira, Bianca</creatorcontrib><creatorcontrib>Misra, Vivek</creatorcontrib><creatorcontrib>Duong, Timothy Q</creatorcontrib><title>Intraarterial transplantation of human umbilical cord blood mononuclear cells in hyperacute stroke improves vascular function</title><title>Stem cell research & therapy</title><addtitle>Stem Cell Res Ther</addtitle><description>Human umbilical cord blood (hUCB) cell therapy is a promising treatment for ischemic stroke. The effects of hyperacute stem cell transplantation on cerebrovascular function in ischemic stroke are, however, not well understood. This study evaluated the effects of hyperacute intraarterial transplantation of hUCB mononuclear cells (MNCs) on cerebrovascular function in stroke rats using serial magnetic resonance imaging (MRI).
HUCB MNCs or vehicle were administered to stroke rats via the internal carotid artery immediately after reperfusion at 60 min following ischemia onset. Lesion volumes were longitudinally evaluated by MRI on days 0, 2, 14, and 28 after stroke, accompanied by behavioral tests. Cerebral blood flow (CBF) and cerebrovascular reactivity were measured by perfusion MRI and CO
functional MRI (fMRI) at 28 days post-stroke; corresponding vascular morphological changes were also detected by immunohistology in the same animals.
We found that CBF to the stroke-affected region at 28 days was improved (normalized CBF value: 1.41 ± 0.30 versus 0.49 ± 0.07) by intraarterial transplantation of hUCB MNCs in the hyperacute stroke phase, compared to vehicle control. Cerebrovascular reactivity within the stroke-affected area, measured by CBF fMRI, was also increased (35.2 ± 3.5% versus 12.8 ± 4.3%), as well as the corresponding cerebrovascular density. Some engrafted cells appeared with microvascular-like morphology and stained positive for von Willebrand Factor (an endothelial cell marker), suggesting they differentiated into endothelial cells. Some engrafted cells also connected to host endothelial cells, suggesting they interacted with the host vasculature. Compared to the vehicle group, infarct volume at 28 days in the stem cell treated group was significantly smaller (160.9 ± 15.7 versus 231.2 ± 16.0 mm
); behavioral deficits were also markedly reduced by stem cell treatment at day 28 (19.5 ± 1.0% versus 30.7 ± 4.7% on the foot fault test; 68.2 ± 4.6% versus 86.6 ± 5.8% on the cylinder test). More tissue within initial perfusion-diffusion mismatch was rescued in the treatment group.
Intraarterial hUCB MNC transplantation during the hyperacute phase of ischemic stroke improved cerebrovascular function and reduced behavioral deficits and infarct volume.</description><subject>Angiogenesis</subject><subject>Animals</subject><subject>Biomarkers - metabolism</subject><subject>Blood flow</subject><subject>Blood Flow Velocity</subject><subject>Bone marrow</subject><subject>Brain Ischemia - metabolism</subject><subject>Brain Ischemia - pathology</subject><subject>Brain Ischemia - therapy</subject><subject>Carbon dioxide</subject><subject>Carotid arteries</subject><subject>Carotid artery</subject><subject>Carotid Artery, Internal</subject><subject>Cell Differentiation</subject><subject>Cell Separation</subject><subject>Cerebral blood flow</subject><subject>Cerebrovascular Circulation</subject><subject>Cerebrovascular system</subject><subject>Cord blood</subject><subject>Cytology</subject><subject>Disease Models, Animal</subject><subject>Endothelial cells</subject><subject>Endothelial Cells - cytology</subject><subject>Endothelial Cells - metabolism</subject><subject>Experiments</subject><subject>Feet</subject><subject>Fetal Blood - cytology</subject><subject>Fetal Blood - metabolism</subject><subject>Functional magnetic resonance imaging</subject><subject>Gene Expression</subject><subject>Heart rate</subject><subject>Humans</subject><subject>Injections, Intra-Arterial</subject><subject>Ischemia</subject><subject>Laboratory animals</subject><subject>Leukocytes (mononuclear)</subject><subject>Leukocytes, Mononuclear - cytology</subject><subject>Leukocytes, Mononuclear - metabolism</subject><subject>Leukocytes, Mononuclear - transplantation</subject><subject>Male</subject><subject>Microvasculature</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Perfusion</subject><subject>Physiology</subject><subject>Postural Balance - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reperfusion</subject><subject>Rodents</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Stroke</subject><subject>Stroke - metabolism</subject><subject>Stroke - pathology</subject><subject>Stroke - therapy</subject><subject>Transplantation</subject><subject>Transplantation, Heterologous</subject><subject>Umbilical cord</subject><subject>Veins & arteries</subject><subject>Von Willebrand factor</subject><subject>von Willebrand Factor - genetics</subject><subject>von Willebrand Factor - metabolism</subject><issn>1757-6512</issn><issn>1757-6512</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</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>eNpdkcFqHSEYhaW0NCHNA2RThG66mVTH0dFNoYQmDQS6adaijvaaOjrV8cJd5N3rcNOQVhAP-P0HjweAC4wuMebsU8Gk52OHcNu0F93hFTjFIx07RnH_-oU-AeelPKC2CEGIDW_BSc-bpAifgsfbuGal8mqzVwE2HcsSVFzV6lOEycFdnVWEddY-eNMQk_IEdUhpgnOKKVYTrMrQ2BAK9BHuDovNytTVwrLm9MtCPy857W2Be1VMDQ12NZrN_x1441Qo9vzpPAP3119_XH3r7r7f3F59uevMIMjaOYsc7pkwxClGnUbUjBgp4bRrQig-CI2mlo3p9iVkYg0gTnOuJ42GkZMz8Pnou1Q928nYLXSQS_azygeZlJf_3kS_kz_TXlLCMB_GZvDxySCn39WWVc6-bJFVtKkWiTlHA2OCkoZ--A99SDXHFm-jKBKECtQofKRMTqVk654fg5Hc-pXHfmXrV279ykObef8yxfPE3zbJH_pYpTM</recordid><startdate>20170322</startdate><enddate>20170322</enddate><creator>Huang, Lei</creator><creator>Liu, Yichu</creator><creator>Lu, Jianfei</creator><creator>Cerqueira, Bianca</creator><creator>Misra, Vivek</creator><creator>Duong, Timothy Q</creator><general>BioMed Central</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</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>20170322</creationdate><title>Intraarterial transplantation of human umbilical cord blood mononuclear cells in hyperacute stroke improves vascular function</title><author>Huang, Lei ; Liu, Yichu ; Lu, Jianfei ; Cerqueira, Bianca ; Misra, Vivek ; Duong, Timothy Q</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-fe0f1269c3fa65fb05c710a9fbfc719a849b0d0066b2873d605c3fb88bdb04783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Angiogenesis</topic><topic>Animals</topic><topic>Biomarkers - metabolism</topic><topic>Blood flow</topic><topic>Blood Flow Velocity</topic><topic>Bone marrow</topic><topic>Brain Ischemia - metabolism</topic><topic>Brain Ischemia - pathology</topic><topic>Brain Ischemia - therapy</topic><topic>Carbon dioxide</topic><topic>Carotid arteries</topic><topic>Carotid artery</topic><topic>Carotid Artery, Internal</topic><topic>Cell Differentiation</topic><topic>Cell Separation</topic><topic>Cerebral blood flow</topic><topic>Cerebrovascular Circulation</topic><topic>Cerebrovascular system</topic><topic>Cord blood</topic><topic>Cytology</topic><topic>Disease Models, Animal</topic><topic>Endothelial cells</topic><topic>Endothelial Cells - cytology</topic><topic>Endothelial Cells - metabolism</topic><topic>Experiments</topic><topic>Feet</topic><topic>Fetal Blood - cytology</topic><topic>Fetal Blood - metabolism</topic><topic>Functional magnetic resonance imaging</topic><topic>Gene Expression</topic><topic>Heart rate</topic><topic>Humans</topic><topic>Injections, Intra-Arterial</topic><topic>Ischemia</topic><topic>Laboratory animals</topic><topic>Leukocytes (mononuclear)</topic><topic>Leukocytes, Mononuclear - cytology</topic><topic>Leukocytes, Mononuclear - metabolism</topic><topic>Leukocytes, Mononuclear - transplantation</topic><topic>Male</topic><topic>Microvasculature</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Perfusion</topic><topic>Physiology</topic><topic>Postural Balance - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reperfusion</topic><topic>Rodents</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><topic>Stroke</topic><topic>Stroke - metabolism</topic><topic>Stroke - pathology</topic><topic>Stroke - therapy</topic><topic>Transplantation</topic><topic>Transplantation, Heterologous</topic><topic>Umbilical cord</topic><topic>Veins & arteries</topic><topic>Von Willebrand factor</topic><topic>von Willebrand Factor - genetics</topic><topic>von Willebrand Factor - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Lei</creatorcontrib><creatorcontrib>Liu, Yichu</creatorcontrib><creatorcontrib>Lu, Jianfei</creatorcontrib><creatorcontrib>Cerqueira, Bianca</creatorcontrib><creatorcontrib>Misra, Vivek</creatorcontrib><creatorcontrib>Duong, Timothy Q</creatorcontrib><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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech 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>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>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content 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>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Stem cell research & therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Lei</au><au>Liu, Yichu</au><au>Lu, Jianfei</au><au>Cerqueira, Bianca</au><au>Misra, Vivek</au><au>Duong, Timothy Q</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intraarterial transplantation of human umbilical cord blood mononuclear cells in hyperacute stroke improves vascular function</atitle><jtitle>Stem cell research & therapy</jtitle><addtitle>Stem Cell Res Ther</addtitle><date>2017-03-22</date><risdate>2017</risdate><volume>8</volume><issue>1</issue><spage>74</spage><epage>74</epage><pages>74-74</pages><artnum>74</artnum><issn>1757-6512</issn><eissn>1757-6512</eissn><abstract>Human umbilical cord blood (hUCB) cell therapy is a promising treatment for ischemic stroke. The effects of hyperacute stem cell transplantation on cerebrovascular function in ischemic stroke are, however, not well understood. This study evaluated the effects of hyperacute intraarterial transplantation of hUCB mononuclear cells (MNCs) on cerebrovascular function in stroke rats using serial magnetic resonance imaging (MRI).
HUCB MNCs or vehicle were administered to stroke rats via the internal carotid artery immediately after reperfusion at 60 min following ischemia onset. Lesion volumes were longitudinally evaluated by MRI on days 0, 2, 14, and 28 after stroke, accompanied by behavioral tests. Cerebral blood flow (CBF) and cerebrovascular reactivity were measured by perfusion MRI and CO
functional MRI (fMRI) at 28 days post-stroke; corresponding vascular morphological changes were also detected by immunohistology in the same animals.
We found that CBF to the stroke-affected region at 28 days was improved (normalized CBF value: 1.41 ± 0.30 versus 0.49 ± 0.07) by intraarterial transplantation of hUCB MNCs in the hyperacute stroke phase, compared to vehicle control. Cerebrovascular reactivity within the stroke-affected area, measured by CBF fMRI, was also increased (35.2 ± 3.5% versus 12.8 ± 4.3%), as well as the corresponding cerebrovascular density. Some engrafted cells appeared with microvascular-like morphology and stained positive for von Willebrand Factor (an endothelial cell marker), suggesting they differentiated into endothelial cells. Some engrafted cells also connected to host endothelial cells, suggesting they interacted with the host vasculature. Compared to the vehicle group, infarct volume at 28 days in the stem cell treated group was significantly smaller (160.9 ± 15.7 versus 231.2 ± 16.0 mm
); behavioral deficits were also markedly reduced by stem cell treatment at day 28 (19.5 ± 1.0% versus 30.7 ± 4.7% on the foot fault test; 68.2 ± 4.6% versus 86.6 ± 5.8% on the cylinder test). More tissue within initial perfusion-diffusion mismatch was rescued in the treatment group.
Intraarterial hUCB MNC transplantation during the hyperacute phase of ischemic stroke improved cerebrovascular function and reduced behavioral deficits and infarct volume.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>28330501</pmid><doi>10.1186/s13287-017-0529-y</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Angiogenesis Animals Biomarkers - metabolism Blood flow Blood Flow Velocity Bone marrow Brain Ischemia - metabolism Brain Ischemia - pathology Brain Ischemia - therapy Carbon dioxide Carotid arteries Carotid artery Carotid Artery, Internal Cell Differentiation Cell Separation Cerebral blood flow Cerebrovascular Circulation Cerebrovascular system Cord blood Cytology Disease Models, Animal Endothelial cells Endothelial Cells - cytology Endothelial Cells - metabolism Experiments Feet Fetal Blood - cytology Fetal Blood - metabolism Functional magnetic resonance imaging Gene Expression Heart rate Humans Injections, Intra-Arterial Ischemia Laboratory animals Leukocytes (mononuclear) Leukocytes, Mononuclear - cytology Leukocytes, Mononuclear - metabolism Leukocytes, Mononuclear - transplantation Male Microvasculature NMR Nuclear magnetic resonance Perfusion Physiology Postural Balance - physiology Rats Rats, Sprague-Dawley Reperfusion Rodents Stem cell transplantation Stem cells Stroke Stroke - metabolism Stroke - pathology Stroke - therapy Transplantation Transplantation, Heterologous Umbilical cord Veins & arteries Von Willebrand factor von Willebrand Factor - genetics von Willebrand Factor - metabolism |
title | Intraarterial transplantation of human umbilical cord blood mononuclear cells in hyperacute stroke improves vascular function |
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