The accelerated engraftment of peripheral blood cell counts following transplantation with hematopoietic stem and progenitor cells (HSCs) mobilized by the CXC chemokine GROβT (CXCL2Δ4) is independent of homing to recipient bone marrow and the SDF1α (CXCL12):CXCR4 migration axis.

被引：0

作者：

Fukuda, S

Bian, HM

King, AG

Pelus, LM

机构：

[1] Indiana Univ, Sch Med, Dept Microbiol Immunol, Indianapolis, IN 46202 USA

[2] Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA

[3] GlaxoSmithKline, Collegeville, PA USA

来源：

BLOOD | 2003年 / 102卷 / 11期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

385

引用

页码：113A / 113A

页数：1

共 6 条

[1] The accelerated engraftment of peripheral blood cell counts following transplantation with hematopoietic stem and progenitor cells (HSCs) mobilized by the CXC chemokine GROβ is independent of the stromal cell-derived factor-1α SDF-1α:CXCR4 migration axis.
Fukuda, S
Bian, HM
Pelus, LM
BLOOD, 2002, 100 (11) : 404B - 405B
[2] Enhanced functional response to CXCL12/SDF-1 through retroviral overexpression of CXCR4: Implications for hematopoietic stem & progenitor cell homing and engraftment.
Christopherson, KW
Porecha, NK
Hangoc, G
Broxmeyer, HE
BLOOD, 2004, 104 (11) : 339A - 339A
[3] The Flt3 ligand/Flt3 axis regulates migration of normal and transformed hematopoietic cells by modulating SDF1α (CXCL12)/CXCR4 signaling.
Fukuda, S
Broxmeyer, HE
Pelus, LM
BLOOD, 2003, 102 (11) : 350A - 350A
[4] Enhanced functional response to CXCL12/SDF-1 through retroviral overexpression of CXCR4 on M07e cells: Implications for hematopoietic stem cell transplantation
Porecha, Nehal K.
English, Kyle
Hangoc, Giao
Broxmeyer, Hal E.
Christopherson, Kent W., II
STEM CELLS AND DEVELOPMENT, 2006, 15 (03) : 325 - 333
[5] Bone marrow stromal cells and the upregulation of interleukin-8 production in human T-cell acute lymphoblastic leukemia through the CXCL12/CXCR4 axis and the NF-κB and JNK/AP-1 pathways
Scupoli, Maria T.
Donadelli, Massimo
Cioffi, Federica
Rossi, Maria
Perbellini, Omar
Malpeli, Giorgio
Corbioli, Silvia
Vinante, Fabrizio
Krampera, Mauro
Palmieri, Marta
Scarpa, Aldo
Ariola, Cristina
Foa, Robin
Pizzolo, Giovanni
HAEMATOLOGICA, 2008, 93 (04) : 524 - 532
[6] Alterations in the stoichiometry and kinetics between matrix metalloproteinase-9 (MMP-9) and tissue inhibitor of metalloproteinase-1 (TIMP-1) are responsible for the synergistic mobilization of peripheral blood hematopoietic stem cells (HSC) by the CXC chemokine GROβT/CXCL2Δ4 plus G-CSF.
Pelus, LM
Bian, HM
King, AG
BLOOD, 2003, 102 (11) : 694A - 695A

← 1 →