The fate of circulating megakaryocytes during cardiopulmonary bypass
Megakaryocytes with intact cytoplasm normally leave the bone marrow, enter central venous blood, and are filtered in the lungs. During cardiopulmonary bypass, large megakaryocytes are not filtered by the lungs and may not be removed in the extracorporeal circuit by arterial line filters. In such cir...
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Veröffentlicht in: | The Journal of thoracic and cardiovascular surgery 1993-10, Vol.106 (4), p.658-663 |
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description | Megakaryocytes with intact cytoplasm normally leave the bone marrow, enter central venous blood, and are filtered in the lungs. During cardiopulmonary bypass, large megakaryocytes are not filtered by the lungs and may not be removed in the extracorporeal circuit by arterial line filters. In such circumstances, they could enter the systemic circulation and block smaller cerebral vessels, resulting in neurologic impairment. To investigate the fate of circulating megakaryocytes during cardiopulmonary bypass, central venous blood and oxygenated blood samples before and after arterial line filtration (40 µm polyester screen filter) were obtained from 10 patients undergoing cardiopulmonary bypass. Megakaryocytes were isolated by whole blood filtration and identified by their characteristic structure after May-Grunwald-Giemsa staining. In preliminary studies, megakaryocyte identification was verified by immunolabeling. All samples contained megakaryocytes with copious cytoplasm. Their frequencies in central venous blood and oxygenated blood before and after the arterial line filtration (corrected for hemodilution) were 23.4 ± 9.3 per milliliter (mean ± standard error of the mean, range 3.1 to 89.7 per milliliter), 21.0 ± 8.2 per milliliter (2.0 to 84.2 per milliliter) and 17.1 ± 7.4 per milliliter (3.1 to 80.4 per milliliter), respectively. Megakaryocytes with scant or no visible cytoplasm were also observed. The results confirm that circulating megakaryocytes are a normal physiologic component. During cardiopulmonary bypass, megakaryocytes with copious cytoplasm (mean diameter 42.7 µm, range 22 to 78 µm) can pass through the extracorporeal circuit. In the absence of filtration by the lungs, these large cells have access to the systemic circulation. This study supports a possible role for circulating megakaryocytes in the development of cerebral dysfunction after cardiopulmonary bypass. (J Thorac Cardiovasc Surg 1993;106:658-63) |
doi_str_mv | 10.1016/S0022-5223(19)33708-0 |
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During cardiopulmonary bypass, large megakaryocytes are not filtered by the lungs and may not be removed in the extracorporeal circuit by arterial line filters. In such circumstances, they could enter the systemic circulation and block smaller cerebral vessels, resulting in neurologic impairment. To investigate the fate of circulating megakaryocytes during cardiopulmonary bypass, central venous blood and oxygenated blood samples before and after arterial line filtration (40 µm polyester screen filter) were obtained from 10 patients undergoing cardiopulmonary bypass. Megakaryocytes were isolated by whole blood filtration and identified by their characteristic structure after May-Grunwald-Giemsa staining. In preliminary studies, megakaryocyte identification was verified by immunolabeling. All samples contained megakaryocytes with copious cytoplasm. Their frequencies in central venous blood and oxygenated blood before and after the arterial line filtration (corrected for hemodilution) were 23.4 ± 9.3 per milliliter (mean ± standard error of the mean, range 3.1 to 89.7 per milliliter), 21.0 ± 8.2 per milliliter (2.0 to 84.2 per milliliter) and 17.1 ± 7.4 per milliliter (3.1 to 80.4 per milliliter), respectively. Megakaryocytes with scant or no visible cytoplasm were also observed. The results confirm that circulating megakaryocytes are a normal physiologic component. During cardiopulmonary bypass, megakaryocytes with copious cytoplasm (mean diameter 42.7 µm, range 22 to 78 µm) can pass through the extracorporeal circuit. In the absence of filtration by the lungs, these large cells have access to the systemic circulation. This study supports a possible role for circulating megakaryocytes in the development of cerebral dysfunction after cardiopulmonary bypass. (J Thorac Cardiovasc Surg 1993;106:658-63)</description><identifier>ISSN: 0022-5223</identifier><identifier>EISSN: 1097-685X</identifier><identifier>DOI: 10.1016/S0022-5223(19)33708-0</identifier><identifier>PMID: 8412260</identifier><identifier>CODEN: JTCSAQ</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>Adult ; Aged ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Cardiopulmonary Bypass ; Cell Count ; Cell Size ; Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care ; Female ; Hemofiltration ; Humans ; Intensive care medicine ; Male ; Medical sciences ; Megakaryocytes - physiology ; Megakaryocytes - ultrastructure ; Middle Aged</subject><ispartof>The Journal of thoracic and cardiovascular surgery, 1993-10, Vol.106 (4), p.658-663</ispartof><rights>1993 American Association for Thoracic Surgery</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-960f287fce06386e3d1e200fbe6d7dd106ae6d73515004e05ebc474aff33a9ba3</citedby><cites>FETCH-LOGICAL-c468t-960f287fce06386e3d1e200fbe6d7dd106ae6d73515004e05ebc474aff33a9ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0022-5223(19)33708-0$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3777926$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8412260$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Woods, M.J.</creatorcontrib><creatorcontrib>Greaves, M.</creatorcontrib><creatorcontrib>Smith, G.H.</creatorcontrib><creatorcontrib>Trowbridge, E.A.</creatorcontrib><title>The fate of circulating megakaryocytes during cardiopulmonary bypass</title><title>The Journal of thoracic and cardiovascular surgery</title><addtitle>J Thorac Cardiovasc Surg</addtitle><description>Megakaryocytes with intact cytoplasm normally leave the bone marrow, enter central venous blood, and are filtered in the lungs. During cardiopulmonary bypass, large megakaryocytes are not filtered by the lungs and may not be removed in the extracorporeal circuit by arterial line filters. In such circumstances, they could enter the systemic circulation and block smaller cerebral vessels, resulting in neurologic impairment. To investigate the fate of circulating megakaryocytes during cardiopulmonary bypass, central venous blood and oxygenated blood samples before and after arterial line filtration (40 µm polyester screen filter) were obtained from 10 patients undergoing cardiopulmonary bypass. Megakaryocytes were isolated by whole blood filtration and identified by their characteristic structure after May-Grunwald-Giemsa staining. In preliminary studies, megakaryocyte identification was verified by immunolabeling. All samples contained megakaryocytes with copious cytoplasm. Their frequencies in central venous blood and oxygenated blood before and after the arterial line filtration (corrected for hemodilution) were 23.4 ± 9.3 per milliliter (mean ± standard error of the mean, range 3.1 to 89.7 per milliliter), 21.0 ± 8.2 per milliliter (2.0 to 84.2 per milliliter) and 17.1 ± 7.4 per milliliter (3.1 to 80.4 per milliliter), respectively. Megakaryocytes with scant or no visible cytoplasm were also observed. The results confirm that circulating megakaryocytes are a normal physiologic component. During cardiopulmonary bypass, megakaryocytes with copious cytoplasm (mean diameter 42.7 µm, range 22 to 78 µm) can pass through the extracorporeal circuit. In the absence of filtration by the lungs, these large cells have access to the systemic circulation. This study supports a possible role for circulating megakaryocytes in the development of cerebral dysfunction after cardiopulmonary bypass. (J Thorac Cardiovasc Surg 1993;106:658-63)</description><subject>Adult</subject><subject>Aged</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Cardiopulmonary Bypass</subject><subject>Cell Count</subject><subject>Cell Size</subject><subject>Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care</subject><subject>Female</subject><subject>Hemofiltration</subject><subject>Humans</subject><subject>Intensive care medicine</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Megakaryocytes - physiology</subject><subject>Megakaryocytes - ultrastructure</subject><subject>Middle Aged</subject><issn>0022-5223</issn><issn>1097-685X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtP3DAURq0KRAfan4CUBaJ0EXptJ3ayqipoCxISi1KpO8uxr2cMeUztBDT_HocZzZaVLX_nPnwIOaVwSYGKb38AGMtLxvgFrb9yLqHK4QNZUKhlLqry3wFZ7JGP5DjGRwCQQOsjclQVlDEBC3L9sMLM6RGzwWXGBzO1evT9MutwqZ902AxmM2LM7BTmV6OD9cN6aruhT2HWbNY6xk_k0Ok24ufdeUL-_vr5cHWT393_vr36cZebQlRjXgtwrJLOIAheCeSWIgNwDQorraUg9HzjJS0BCoQSG1PIQjvHua4bzU_I-bbvOgz_J4yj6nw02La6x2GKSgqAmjNIYLkFTRhiDOjUOvguLawoqNmeerOnZjWK1urNnprrTncDpqZDu6_a6Ur52S7X0ejWBd0bH_cYl1LWTCTsyxZb-eXqxQdUsdNtm5pS9TiamH6qCiXKKpHftyQmbc8eg4rGY2_QpiozKjv4d1Z-BbY2maU</recordid><startdate>19931001</startdate><enddate>19931001</enddate><creator>Woods, M.J.</creator><creator>Greaves, M.</creator><creator>Smith, G.H.</creator><creator>Trowbridge, E.A.</creator><general>Elsevier Inc</general><general>AATS/WTSA</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><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>19931001</creationdate><title>The fate of circulating megakaryocytes during cardiopulmonary bypass</title><author>Woods, M.J. ; Greaves, M. ; Smith, G.H. ; Trowbridge, E.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-960f287fce06386e3d1e200fbe6d7dd106ae6d73515004e05ebc474aff33a9ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Cardiopulmonary Bypass</topic><topic>Cell Count</topic><topic>Cell Size</topic><topic>Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care</topic><topic>Female</topic><topic>Hemofiltration</topic><topic>Humans</topic><topic>Intensive care medicine</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Megakaryocytes - physiology</topic><topic>Megakaryocytes - ultrastructure</topic><topic>Middle Aged</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woods, M.J.</creatorcontrib><creatorcontrib>Greaves, M.</creatorcontrib><creatorcontrib>Smith, G.H.</creatorcontrib><creatorcontrib>Trowbridge, E.A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><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>The Journal of thoracic and cardiovascular surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woods, M.J.</au><au>Greaves, M.</au><au>Smith, G.H.</au><au>Trowbridge, E.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The fate of circulating megakaryocytes during cardiopulmonary bypass</atitle><jtitle>The Journal of thoracic and cardiovascular surgery</jtitle><addtitle>J Thorac Cardiovasc Surg</addtitle><date>1993-10-01</date><risdate>1993</risdate><volume>106</volume><issue>4</issue><spage>658</spage><epage>663</epage><pages>658-663</pages><issn>0022-5223</issn><eissn>1097-685X</eissn><coden>JTCSAQ</coden><abstract>Megakaryocytes with intact cytoplasm normally leave the bone marrow, enter central venous blood, and are filtered in the lungs. During cardiopulmonary bypass, large megakaryocytes are not filtered by the lungs and may not be removed in the extracorporeal circuit by arterial line filters. In such circumstances, they could enter the systemic circulation and block smaller cerebral vessels, resulting in neurologic impairment. To investigate the fate of circulating megakaryocytes during cardiopulmonary bypass, central venous blood and oxygenated blood samples before and after arterial line filtration (40 µm polyester screen filter) were obtained from 10 patients undergoing cardiopulmonary bypass. Megakaryocytes were isolated by whole blood filtration and identified by their characteristic structure after May-Grunwald-Giemsa staining. In preliminary studies, megakaryocyte identification was verified by immunolabeling. All samples contained megakaryocytes with copious cytoplasm. Their frequencies in central venous blood and oxygenated blood before and after the arterial line filtration (corrected for hemodilution) were 23.4 ± 9.3 per milliliter (mean ± standard error of the mean, range 3.1 to 89.7 per milliliter), 21.0 ± 8.2 per milliliter (2.0 to 84.2 per milliliter) and 17.1 ± 7.4 per milliliter (3.1 to 80.4 per milliliter), respectively. Megakaryocytes with scant or no visible cytoplasm were also observed. The results confirm that circulating megakaryocytes are a normal physiologic component. During cardiopulmonary bypass, megakaryocytes with copious cytoplasm (mean diameter 42.7 µm, range 22 to 78 µm) can pass through the extracorporeal circuit. In the absence of filtration by the lungs, these large cells have access to the systemic circulation. This study supports a possible role for circulating megakaryocytes in the development of cerebral dysfunction after cardiopulmonary bypass. (J Thorac Cardiovasc Surg 1993;106:658-63)</abstract><cop>Philadelphia, PA</cop><pub>Elsevier Inc</pub><pmid>8412260</pmid><doi>10.1016/S0022-5223(19)33708-0</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Cardiopulmonary Bypass Cell Count Cell Size Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care Female Hemofiltration Humans Intensive care medicine Male Medical sciences Megakaryocytes - physiology Megakaryocytes - ultrastructure Middle Aged |
title | The fate of circulating megakaryocytes during cardiopulmonary bypass |
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