Selective Deamidation of Recombinant Human Stem Cell Factor during in Vitro Aging:  Isolation and Characterization of the Aspartyl and Isoaspartyl Homodimers and Heterodimers

Biochemistry ◽  
1998 ◽  
Vol 37 (8) ◽  
pp. 2251-2262 ◽  
Author(s):  
Yueh-Rong Hsu ◽  
Chang ◽  
Elizabeth A. Mendiaz ◽  
Shinichi Hara ◽  
David T. Chow ◽  
...  
1996 ◽  
Vol 271 (19) ◽  
pp. 11309-11316 ◽  
Author(s):  
Hsieng S. Lu ◽  
Michael D. Jones ◽  
Jae-Hung Shieh ◽  
Elizabeth A. Mendiaz ◽  
Daphne Feng ◽  
...  

2017 ◽  
Vol 64 (4) ◽  
pp. 509-518 ◽  
Author(s):  
Liang-hua Chen ◽  
Feng Cai ◽  
Dan-ju Zhang ◽  
Li Zhang ◽  
Peng Zhu ◽  
...  

1991 ◽  
Vol 148 (3) ◽  
pp. 503-509 ◽  
Author(s):  
Giovanni Migliaccio ◽  
Anna Rita Migliaccio ◽  
Maurice L. Druzin ◽  
Patricia-Jane V. Giardina ◽  
Krisztina M. Zsebo ◽  
...  

Blood ◽  
1991 ◽  
Vol 78 (8) ◽  
pp. 1975-1980 ◽  
Author(s):  
RG Andrews ◽  
GH Knitter ◽  
SH Bartelmez ◽  
KE Langley ◽  
D Farrar ◽  
...  

Abstract Recombinant human stem cell factor (SCF) is homologous with recombinant rat SCF (rrSCF) and is a ligand for c-kit. We determined the influence of SCF on hematopoiesis in vitro and in vivo in baboons. In vitro, SCF alone stimulated little growth of hematopoietic colony-forming cells from baboon marrow, but did increase the number of colonies formed in response to erythropoietin (Epo), interleukin-3 (IL-3), and granulocyte- macrophage colony-stimulating factor (GM-CSF). In vivo, SCF caused an increase in the peripheral blood of the number of erythrocytes, neutrophils, lymphocytes, monocytes, eosinophils, and basophils. In marrow, it caused an increase in marrow cellularity and in the absolute number of colony-forming unit-granulocyte-monocyte (CFU-GM) and burst- forming unit-erythroid (BFU-E) in marrow following infusion of SCF. The in vivo stimulation of multiple lymphohematopoietic lineages corroborates previous in vitro studies and suggests a potentially important clinical role for SCF.


1998 ◽  
Vol 16 ◽  
pp. S96
Author(s):  
Francesca Prignano ◽  
Gianni Gerlini ◽  
Nicola Pimpinelli ◽  
Paolo Romagnoli ◽  
Benvenuto Giannotti

Blood ◽  
1991 ◽  
Vol 78 (8) ◽  
pp. 1975-1980 ◽  
Author(s):  
RG Andrews ◽  
GH Knitter ◽  
SH Bartelmez ◽  
KE Langley ◽  
D Farrar ◽  
...  

Recombinant human stem cell factor (SCF) is homologous with recombinant rat SCF (rrSCF) and is a ligand for c-kit. We determined the influence of SCF on hematopoiesis in vitro and in vivo in baboons. In vitro, SCF alone stimulated little growth of hematopoietic colony-forming cells from baboon marrow, but did increase the number of colonies formed in response to erythropoietin (Epo), interleukin-3 (IL-3), and granulocyte- macrophage colony-stimulating factor (GM-CSF). In vivo, SCF caused an increase in the peripheral blood of the number of erythrocytes, neutrophils, lymphocytes, monocytes, eosinophils, and basophils. In marrow, it caused an increase in marrow cellularity and in the absolute number of colony-forming unit-granulocyte-monocyte (CFU-GM) and burst- forming unit-erythroid (BFU-E) in marrow following infusion of SCF. The in vivo stimulation of multiple lymphohematopoietic lineages corroborates previous in vitro studies and suggests a potentially important clinical role for SCF.


2005 ◽  
Vol 43 (2) ◽  
pp. 126-132 ◽  
Author(s):  
Haiqin Lu ◽  
Yuhui Zang ◽  
Yuguan Ze ◽  
Jie Zhu ◽  
Tao Chen ◽  
...  

Blood ◽  
1996 ◽  
Vol 87 (8) ◽  
pp. 3203-3211 ◽  
Author(s):  
MK Majumdar ◽  
ET Everett ◽  
X Xiao ◽  
R Cooper ◽  
K Langley ◽  
...  

Mutations of c-kit, which encodes a transmembrane receptor tyrosine kinase, have been identified in mice by abnormal coat color, anemia, and germ cell defects. Mice heterozygous for mutations of c-kit have a white forehead blaze and a white ventral spot, leading these mutants to be termed dominant White spotting (W). We have previously demonstrated that the membrane-associated isoform of human stem cell factor (hSCF220, the ligand for c-kit) is inefficiently processed in murine stromal cell transfectants. Thus, in murine cell lines analyzed in vitro, hSCF220 transfectants present SCF as a membrane restricted protein in contrast to the murine SCF220 cDNA protein product, which is slowly cleaved and secreted. We show here that transgenic mice expressing the human SCF220 isoform in vivo display a phenotype indistinguishable from some alleles of W. Specifically, hSCF220- expressing transgenic mice display a prominent forehead blaze and a white ventral spot. Generations of doubly heterozygous animals that carry both a mutated c-kit allele and the hSCF220 transgene display a more severe coat color abnormality. This phenotype appears to be due to occupancy of murine c-kit by human SCF and diminished cell surface expression of endogenous murine SCF. Normal signaling events that lead to cell survival or proliferation appear to be disrupted in vivo in these transgenic mice.


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