Splenectomy influences homing of transplanted stem cells in bone marrow-ablated mice
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21651380
DOI
10.1089/scd.2011.0068
Knihovny.cz E-zdroje
- MeSH
- beta-galaktosidasa genetika metabolismus MeSH
- časové faktory MeSH
- exprese genu MeSH
- hematopoetické kmenové buňky cytologie metabolismus MeSH
- hematopoéza účinky záření MeSH
- imunohistochemie MeSH
- kostní dřeň metabolismus účinky záření MeSH
- myši kmene 129 MeSH
- myši transgenní MeSH
- myši MeSH
- počet lymfocytů MeSH
- pohyb buněk * MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- proliferační antigen buněčného jádra metabolismus MeSH
- protoonkogenní proteiny c-kit metabolismus MeSH
- průtoková cytometrie MeSH
- splenektomie metody MeSH
- thymus cytologie metabolismus MeSH
- transplantace kostní dřeně MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- beta-galaktosidasa MeSH
- proliferační antigen buněčného jádra MeSH
- protoonkogenní proteiny c-kit MeSH
Cell mobilization, a process that influences circulation, margination, and finally, homing play key roles in the regeneration processes mediated by stem cells. Recent studies as well as prior studies from our group indicate an important role of the spleen in hematopoietic reconstitution, but to date the role of the spleen in hematopoietic reconstitution has been unclear and it has not been precisely documented in ablated animals. Therefore, we undertook the present study to define more closely the role of the spleen in hematopoietic reconstitution in lethally irradiated mice. After transplantation of irradiated mice with lacZ+ -marked lin- / CD117+ bone marrow cells, we compared splenectomized mice (T(S), splenectomy performed prior to irradiation) to nonsplenectomized, irradiated mice (T(N)) as well as to normal (unirradiated) mice. Impaired hematopoietic reconstitution was observed in T(S) mice. Splenectomy markedly altered the distribution of hematopoietic stem cells, as demonstrated by fluorescence-activated cell sorting analysis of endogenous CD117+ cells in the thymus and bone marrow of recipients. Cell engraftment was demonstrated by histochemical and polymerase chain reaction analyses of recipient tissues. These experiments demonstrated that in T(S) animals, transplanted hematopoietic stem cells mobilized to extravascular tissues, particularly the gastrointestinal tract. The number of donor cells in recipient tissues continued to increase for 30 days after transplantation with the highest numbers observed in the T(S) group. DNA marking analysis led to the conclusion that engrafted cells were not only integrated into recipient tissues but were also capable of performing complex cellular processes, including proliferation and repair. Our results are consistent with the novel possibility that cellular repair markedly affects stem cell regenerative functions and that repair is markedly influenced by the integrity and presence of organs not directly involved in specific tissue regeneration processes, particularly the spleen.
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