Characterization of the Molecules Involved in the Hematopoietic Microenvironment Provided by Mouse Stromal Cell Line MC3T3-G2/PA6 Using a Unique Reporter System That Analyzes the Direct Cell-to-Cell Interaction

1997 ◽  
Vol 98 (2) ◽  
pp. 95-103 ◽  
Author(s):  
Mitsuo Satoh ◽  
Hiroyuki Mioh ◽  
Noboru Konishi ◽  
Isami Takahashi ◽  
Tasuya Tamaoki
Endocrinology ◽  
1995 ◽  
Vol 136 (4) ◽  
pp. 1441-1449 ◽  
Author(s):  
S Takahashi ◽  
S V Reddy ◽  
M Dallas ◽  
R Devlin ◽  
J Y Chou ◽  
...  

Bone ◽  
1995 ◽  
Vol 17 (6) ◽  
pp. 573
Author(s):  
P. Smits ◽  
J. Bhalerao ◽  
P. Tylzanowski ◽  
C.A. Kozak ◽  
J. Merrceaert

Blood ◽  
1998 ◽  
Vol 91 (4) ◽  
pp. 1263-1271 ◽  
Author(s):  
Takashi Tsuji ◽  
Iwao Waga ◽  
Katsunari Tezuka ◽  
Masafumi Kamada ◽  
Kimio Yatsunami ◽  
...  

Abstract Cellular interactions between hematopoietic cells and stromal cells play important roles in the proliferation and differentiation of hematopoietic cells. The proliferation of a human erythroleukemia cell line, HEL cells, which can differentiate into macrophage- and megakaryocyte-like cells, and erythroid precursors was dramatically induced on coculture with a hematopoietic-supportive stromal cell line, HESS-5 cells, which can support long-term hematopoiesis in vitro without fetal bovine serum. HEL cells proliferated when they were cocultured with but not without direct cell contact. Because the coculture supernatants with direct cell contact and cytokines such as interleukins and growth factors did not exhibit growth-stimulating activity toward HEL cells, it was suggested that some molecule that has growth-stimulating activity exists on the surface of the cells. Extracellular matrix components such as fibronectin, laminin, vitronectin, and collagen did not affect the proliferation of HEL cells. An anti-CD18 monoclonal antibody, which recognizes the common β chain of the β2 integrin subfamily, induced dramatic proliferation of HEL cells. Moreover, the proliferation of HEL cells was inhibited by an antisense oligonucleotide of CD18 mRNA. As judged from these observations, the proliferation of HEL cells was mediated by CD18 molecules expressed on HEL cells. On the contrary, the common counter-receptor of the β2 integrin subfamily, intercellular adhesion molecule-1, which is expressed on CHO-K1 cells, did not stimulate the growth of HEL cells. It is known that other counter molecules of the β2 integrin subfamily, such as complement C3bi and fibrinogen, are not produced by stromal cells. These findings suggest that the proliferation of HEL cells may be induced through an interaction between a novel molecule of the β2 integrin subfamily on HEL cells and the counter-receptor on HESS-5 cells. The β2 integrin subfamily may regulate the growth of hematopoietic cells in hematopoiesis in vivo and/or cause the abnormal growth of leukemia cells.


1988 ◽  
Vol 167 (3) ◽  
pp. 988-1002 ◽  
Author(s):  
A E Namen ◽  
A E Schmierer ◽  
C J March ◽  
R W Overell ◽  
L S Park ◽  
...  

We have used a biological assay system we developed to biochemically purify a previously uncharacterized murine lymphopoietic growth factor designated lymphopoietin 1 (LP-1). This factor is capable of stimulating the proliferation and extended maintenance of precursor cells of the B lineage. A stromal cell line producing LP-1 was established after transfection of primary stromal cultures with a plasmid encoding the transforming genes of SV40. This factor was purified to a single 25-kD species from the culture supernatant of an adherent stromal cell line. This material acts on immature lymphocytes, it binds to specific receptors on cells, and is distinct from previously described hematopoietic factors. LP-1 has been purified some 10(7)-fold with an overall recovery of 35%. The purified protein exhibits a specific activity of approximately 4 X 10(6) U/micrograms of protein and is active at a half-maximal concentration of 10(-13) M.


1995 ◽  
Vol 5 (6) ◽  
pp. 441-457 ◽  
Author(s):  
M.L. Diago ◽  
M.P. López-Fierro ◽  
B. Razquin ◽  
A. Villena

2000 ◽  
Vol 192 (5) ◽  
pp. 671-680 ◽  
Author(s):  
John E. Sims ◽  
Douglas E. Williams ◽  
Philip J. Morrissey ◽  
Kirsten Garka ◽  
Diane Foxworthe ◽  
...  

Using a bioassay consisting of the proliferation of a murine B cell line, a cDNA of a gene whose product supports the growth of that cell line was isolated from a thymic stromal cell line. This factor, termed thymic stromal lymphopoietin (TSLP), is a protein of 140 amino acids. The gene encoding TSLP was mapped to murine chromosome 18. Purified recombinant TSLP supported the growth of pre-B cell colonies in vitro, but had no myelopoietic activity. TSLP had comitogenic activity for fetal thymocytes, but was not as potent as interleukin 7 in lobe submersion cultures. Injection of TSLP into neonatal mice induced the expansion of B220+BP-1+ pre-B cells.


1997 ◽  
Vol 272 (4) ◽  
pp. 2570-2577 ◽  
Author(s):  
Ryuta Koishi ◽  
Ichiro Kawashima ◽  
Chigusa Yoshimura ◽  
Mie Sugawara ◽  
Nobufusa Serizawa

1995 ◽  
Vol 2 (4) ◽  
pp. 330-342
Author(s):  
Suzanne Gartner ◽  
Stephan W. Kessler ◽  
Vince F. La Russa ◽  
Jerome H. Kim ◽  
Richard G. Carroll ◽  
...  

2019 ◽  
Vol 116 (6) ◽  
pp. 1417-1426 ◽  
Author(s):  
Janina Burk ◽  
Heidrun Holland ◽  
Anne F. Lauermann ◽  
Tobias May ◽  
Philipp Siedlaczek ◽  
...  

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