dc.contributor.author |
Horváth, Zsuzsanna |
|
dc.contributor.author |
Pállinger, Éva |
|
dc.contributor.author |
Horvath G |
|
dc.contributor.author |
Jelinek I |
|
dc.contributor.author |
Veszely G |
|
dc.contributor.author |
Furesz J |
|
dc.contributor.author |
Falus, András |
|
dc.contributor.author |
Buzás, Edit Irén |
|
dc.date.accessioned |
2018-10-12T08:10:01Z |
|
dc.date.available |
2018-10-12T08:10:01Z |
|
dc.date.issued |
2010 |
|
dc.identifier |
77953323274 |
|
dc.identifier.citation |
pagination=429-436;
journalVolume=59;
journalIssueNumber=6;
journalTitle=INFLAMMATION RESEARCH; |
|
dc.identifier.uri |
http://repo.lib.semmelweis.hu//handle/123456789/4826 |
|
dc.identifier.uri |
doi:10.1007/s00011-009-0114-7 |
|
dc.description.abstract |
OBJECTIVE AND DESIGN: In this study we investigated the role of histamine on the extramedullary hematopoiesis. METHODS: Male histidine decarboxylase knockout (HDC(-/-)) mice and wild-type mice were used (n = 5/group). Groups of mice received sublethal total-body gamma irradiation at a single dose of 4 Gy. Spleen cells were studied at different time points post-irradiation by flow cytometry, colony forming unit (CFU) assay, and real-time PCR. For statistical analysis Student's t test, ANOVA, and Holm-Sidak post-hoc test were used. RESULTS: By day 14 after irradiation, spleen cell counts increased almost eightfold in wild-type and not even fourfold in HDC(-/-) mice (P < 0.01). The proliferative capacity and interleukin-3 signaling of stem cells were impaired in HDC(-/-) mice. STAT5 mRNA expression was decreased in granulocyte-myeloid colonies by 72.9 +/- 8.6% (P < 0.001), compared to the wild-type. CONCLUSIONS: The absence of histamine adversely affects splenic hematopoiesis via direct and indirect mechanisms. |
|
dc.relation.ispartof |
urn:issn:1023-3830 |
|
dc.title |
Extramedullary hematopoiesis is dysregulated in histamine-free histidine decarboxylase knockout (HDC-/-) mice. |
|
dc.type |
Journal Article |
|
dc.date.updated |
2018-02-16T13:46:29Z |
|
dc.language.rfc3066 |
en |
|
dc.identifier.mtmt |
1392681 |
|
dc.identifier.wos |
000277641200004 |
|
dc.identifier.pubmed |
19921486 |
|
dc.contributor.department |
SE/AOK/I/Genetikai, Sejt- és Immunbiológiai Intézet |
|
dc.contributor.institution |
Semmelweis Egyetem |
|