dc.contributor.author
Wong, David
dc.contributor.author
Winter, Oliver
dc.contributor.author
Hartig, Christina
dc.contributor.author
Siebels, Svenja
dc.contributor.author
Szyska, Martin
dc.contributor.author
Tiburzy, Benjamin
dc.contributor.author
Meng, Lingzhang
dc.contributor.author
Kulkarni, Upasana
dc.contributor.author
Fähnrich, Anke
dc.contributor.author
Bommert, Kurt
dc.contributor.author
Bargou, Ralf
dc.contributor.author
Berek, Claudia
dc.contributor.author
Chu, Van Trung
dc.contributor.author
Bogen, Bjarne
dc.contributor.author
Jundt, Franziska
dc.contributor.author
Manz, Rudolf Armin
dc.date.accessioned
2018-06-08T03:04:19Z
dc.date.available
2014-12-01T10:21:54.661Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/14450
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-18643
dc.description.abstract
Multiple myeloma is a bone marrow plasma cell tumor which is supported by the
external growth factors APRIL and IL-6, among others. Recently, we identified
eosinophils and megakaryocytes to be functional components of the micro-
environmental niches of benign bone marrow plasma cells and to be important
local sources of these cytokines. Here, we investigated whether eosinophils
and megakaryocytes also support the growth of tumor plasma cells in the
MOPC315.BM model for multiple myeloma. As it was shown for benign plasma cells
and multiple myeloma cells, IL-6 and APRIL also supported MOPC315.BM cell
growth in vitro, IL-5 had no effect. Depletion of eosinophils in vivo by IL-5
blockade led to a reduction of the early myeloma load. Consistent with this,
myeloma growth in early stages was retarded in eosinophil-deficient ΔdblGATA-1
mice. Late myeloma stages were unaffected, possibly due to megakaryocytes
compensating for the loss of eosinophils, since megakaryocytes were found to
be in contact with myeloma cells in vivo and supported myeloma growth in
vitro. We conclude that eosinophils and megakaryocytes in the niches for
benign bone marrow plasma cells support the growth of malignant plasma cells.
Further investigations are required to test whether perturbation of these
niches represents a potential strategy for the treatment of multiple myeloma.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
Eosinophils and Megakaryocytes Support the Early Growth of Murine MOPC315
Myeloma Cells in Their Bone Marrow Niches
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
PLoS ONE. - 9 (2014), 10, Artikel Nr. e109018
dcterms.bibliographicCitation.doi
10.1371/journal.pone.0109018
dcterms.bibliographicCitation.url
http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0109018
refubium.affiliation
Charité - Universitätsmedizin Berlin
de
refubium.mycore.fudocsId
FUDOCS_document_000000021379
refubium.note.author
Der Artikel wurde in einer Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000004210
dcterms.accessRights.openaire
open access