Cellular composition of lymph in experimental lymphedema.
Identifieur interne : 009501 ( Ncbi/Merge ); précédent : 009500; suivant : 009502Cellular composition of lymph in experimental lymphedema.
Auteurs : H. Galkowska ; W L OlszewskiSource :
- Lymphology [ 0024-7766 ] ; 1986.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Lymphoedème.
- cytologie : Lymphe.
- immunologie : Lymphe, Lymphoedème.
- pharmacologie : Mitogènes.
- Activation des lymphocytes, Animaux, Chiens, Cytotoxicité immunologique, Numération cellulaire, Récepteur Fc, Récepteurs au C3b du complément, Récepteurs au complément.
English descriptors
- KwdEn :
- MESH :
- chemical , pharmacology : Mitogens.
- cytology : Lymph.
- immunology : Lymph, Lymphedema.
- pathology : Lymphedema.
- Animals, Cell Count, Cytotoxicity, Immunologic, Dogs, Lymphocyte Activation, Receptors, Complement, Receptors, Complement 3b, Receptors, Fc.
Abstract
Lymph cell populations were characterized immunologically in dogs with chronic post-surgical lymphedema. There was a 10- to 30-fold increase in lymph total cell count as compared with normal (control) dogs. Morphologically, these were predominantly small lymphocytes with approximately 4-6% monocytes and veiled cells. In contrast, lymph from normal dogs contained 33% granulocytes and 27% monocytes. The Fc-R+ and C3b-R+ mononuclear nonadherent cells were less represented in lymph in chronic stasis than in normals. A high autotransformation rate of lymph cells and marked responsiveness to PHA and Con A were also observed. In chronic lymphedema K-cell and NK-cell cytotoxicity were lower than in normal lymph. Interruption or retardation of the lymphocyte recirculation pathway with lymph stasis may alter regulation of immune responsiveness in lymphedematous tissue.
PubMed: 2951567
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 006515
- to stream PubMed, to step Curation: 006515
- to stream PubMed, to step Checkpoint: 006515
Links to Exploration step
pubmed:2951567Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Cellular composition of lymph in experimental lymphedema.</title><author><name sortKey="Galkowska, H" sort="Galkowska, H" uniqKey="Galkowska H" first="H" last="Galkowska">H. Galkowska</name></author><author><name sortKey="Olszewski, W L" sort="Olszewski, W L" uniqKey="Olszewski W" first="W L" last="Olszewski">W L Olszewski</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="1986">1986</date><idno type="RBID">pubmed:2951567</idno><idno type="pmid">2951567</idno><idno type="wicri:Area/PubMed/Corpus">006515</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">006515</idno><idno type="wicri:Area/PubMed/Curation">006515</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">006515</idno><idno type="wicri:Area/PubMed/Checkpoint">006515</idno><idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">006515</idno><idno type="wicri:Area/Ncbi/Merge">009501</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Cellular composition of lymph in experimental lymphedema.</title><author><name sortKey="Galkowska, H" sort="Galkowska, H" uniqKey="Galkowska H" first="H" last="Galkowska">H. Galkowska</name></author><author><name sortKey="Olszewski, W L" sort="Olszewski, W L" uniqKey="Olszewski W" first="W L" last="Olszewski">W L Olszewski</name></author></analytic><series><title level="j">Lymphology</title><idno type="ISSN">0024-7766</idno><imprint><date when="1986" type="published">1986</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Cell Count</term><term>Cytotoxicity, Immunologic</term><term>Dogs</term><term>Lymph (cytology)</term><term>Lymph (immunology)</term><term>Lymphedema (immunology)</term><term>Lymphedema (pathology)</term><term>Lymphocyte Activation</term><term>Mitogens (pharmacology)</term><term>Receptors, Complement</term><term>Receptors, Complement 3b</term><term>Receptors, Fc</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Activation des lymphocytes</term><term>Animaux</term><term>Chiens</term><term>Cytotoxicité immunologique</term><term>Lymphe (cytologie)</term><term>Lymphe (immunologie)</term><term>Lymphoedème (anatomopathologie)</term><term>Lymphoedème (immunologie)</term><term>Mitogènes (pharmacologie)</term><term>Numération cellulaire</term><term>Récepteur Fc</term><term>Récepteurs au C3b du complément</term><term>Récepteurs au complément</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Mitogens</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Lymphoedème</term></keywords><keywords scheme="MESH" qualifier="cytologie" xml:lang="fr"><term>Lymphe</term></keywords><keywords scheme="MESH" qualifier="cytology" xml:lang="en"><term>Lymph</term></keywords><keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Lymphe</term><term>Lymphoedème</term></keywords><keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Lymph</term><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Mitogènes</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Cell Count</term><term>Cytotoxicity, Immunologic</term><term>Dogs</term><term>Lymphocyte Activation</term><term>Receptors, Complement</term><term>Receptors, Complement 3b</term><term>Receptors, Fc</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Activation des lymphocytes</term><term>Animaux</term><term>Chiens</term><term>Cytotoxicité immunologique</term><term>Numération cellulaire</term><term>Récepteur Fc</term><term>Récepteurs au C3b du complément</term><term>Récepteurs au complément</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Lymph cell populations were characterized immunologically in dogs with chronic post-surgical lymphedema. There was a 10- to 30-fold increase in lymph total cell count as compared with normal (control) dogs. Morphologically, these were predominantly small lymphocytes with approximately 4-6% monocytes and veiled cells. In contrast, lymph from normal dogs contained 33% granulocytes and 27% monocytes. The Fc-R+ and C3b-R+ mononuclear nonadherent cells were less represented in lymph in chronic stasis than in normals. A high autotransformation rate of lymph cells and marked responsiveness to PHA and Con A were also observed. In chronic lymphedema K-cell and NK-cell cytotoxicity were lower than in normal lymph. Interruption or retardation of the lymphocyte recirculation pathway with lymph stasis may alter regulation of immune responsiveness in lymphedematous tissue.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">2951567</PMID><DateCreated><Year>1987</Year><Month>05</Month><Day>14</Day></DateCreated><DateCompleted><Year>1987</Year><Month>05</Month><Day>14</Day></DateCompleted><DateRevised><Year>2006</Year><Month>11</Month><Day>03</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0024-7766</ISSN><JournalIssue CitedMedium="Print"><Volume>19</Volume><Issue>4</Issue><PubDate><Year>1986</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Lymphology</Title><ISOAbbreviation>Lymphology</ISOAbbreviation></Journal><ArticleTitle>Cellular composition of lymph in experimental lymphedema.</ArticleTitle><Pagination><MedlinePgn>139-45</MedlinePgn></Pagination><Abstract><AbstractText>Lymph cell populations were characterized immunologically in dogs with chronic post-surgical lymphedema. There was a 10- to 30-fold increase in lymph total cell count as compared with normal (control) dogs. Morphologically, these were predominantly small lymphocytes with approximately 4-6% monocytes and veiled cells. In contrast, lymph from normal dogs contained 33% granulocytes and 27% monocytes. The Fc-R+ and C3b-R+ mononuclear nonadherent cells were less represented in lymph in chronic stasis than in normals. A high autotransformation rate of lymph cells and marked responsiveness to PHA and Con A were also observed. In chronic lymphedema K-cell and NK-cell cytotoxicity were lower than in normal lymph. Interruption or retardation of the lymphocyte recirculation pathway with lymph stasis may alter regulation of immune responsiveness in lymphedematous tissue.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Galkowska</LastName><ForeName>H</ForeName><Initials>H</Initials></Author><Author ValidYN="Y"><LastName>Olszewski</LastName><ForeName>W L</ForeName><Initials>WL</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Lymphology</MedlineTA><NlmUniqueID>0155112</NlmUniqueID><ISSNLinking>0024-7766</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008934">Mitogens</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011951">Receptors, Complement</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D017463">Receptors, Complement 3b</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011961">Receptors, Fc</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002452" MajorTopicYN="N">Cell Count</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003602" MajorTopicYN="N">Cytotoxicity, Immunologic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004285" MajorTopicYN="N">Dogs</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008196" MajorTopicYN="N">Lymph</DescriptorName><QualifierName UI="Q000166" MajorTopicYN="Y">cytology</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008213" MajorTopicYN="N">Lymphocyte Activation</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008934" MajorTopicYN="N">Mitogens</DescriptorName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011951" MajorTopicYN="N">Receptors, Complement</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017463" MajorTopicYN="N">Receptors, Complement 3b</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011961" MajorTopicYN="N">Receptors, Fc</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1986</Year><Month>12</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1986</Year><Month>12</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1986</Year><Month>12</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">2951567</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list></list><tree><noCountry><name sortKey="Galkowska, H" sort="Galkowska, H" uniqKey="Galkowska H" first="H" last="Galkowska">H. Galkowska</name><name sortKey="Olszewski, W L" sort="Olszewski, W L" uniqKey="Olszewski W" first="W L" last="Olszewski">W L Olszewski</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Ncbi/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 009501 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd -nk 009501 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= Ncbi
|étape= Merge
|type= RBID
|clé= pubmed:2951567
|texte= Cellular composition of lymph in experimental lymphedema.
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Merge/RBID.i -Sk "pubmed:2951567" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Merge/biblio.hfd \
| NlmPubMed2Wicri -a LymphedemaV1
| This area was generated with Dilib version V0.6.31. |  |