Changes in cell surface molecules associated with in vitro culture of prostatic stromal cells

The Prostate ◽  
2000 ◽  
Vol 44 (4) ◽  
pp. 303-312 ◽  
Author(s):  
Alvin Y. Liu ◽  
Leah LaTray ◽  
Ger van den Engh
1994 ◽  
Vol 154 (2) ◽  
pp. 498-506 ◽  
Author(s):  
Manuela Santos ◽  
Maria de Sousa

2007 ◽  
Vol 361-363 ◽  
pp. 1153-1156
Author(s):  
Jeong Joon Yoo ◽  
Kwang Woo Nam ◽  
Kyung Hoi Koo ◽  
Kang Sup Yoon ◽  
Hee Joong Kim

The unique characteristics of cell surface molecules on human bone marrow stromal cells (hBMSCs) have not been clearly elucidated. The authors characterized 19 cell surface molecules on culture-expanded hBMSCs obtained from 10 human donors, by flow cytometry, calculated the averages and standard deviations of the expression frequencies of individual surface molecules, and evaluated their expression patterns with respect to donor-dependent variations. Surface molecules expressed at frequencies of more than 80% on cells included, CD49e, CD29, CD90, CD73, CD44, CD105, and CD146, those expressed at frequencies of 20-80% included, Stro-1, CD51, CD54, CD31, CD106, CD163, and CD34, whereas CD49d, CD14, CD144, CD11b, and CD45 were expressed at less than 20%. Substantial donor-dependent variations (>10% standard deviation in expression percentage) were observed in the expressions of CD105, Stro-1, CD51, CD54, CD31, CD106, CD163, and CD34. Our results demonstrate that CD49e, CD29, CD90, CD73, and CD44 can be used as a positive marker for hBMSCs, and that CD144, CD11b, and CD45 could be used as a highly selective negative marker. However, the expressions of CD54, CD31, and CD106 observed in the present study, contradicted prior reports and thus, their expressions remain controversial.


Parasitology ◽  
1995 ◽  
Vol 110 (5) ◽  
pp. 503-511 ◽  
Author(s):  
J. Iqbal ◽  
A. B. Siddique ◽  
N. Ahlborg ◽  
P. Perlmann ◽  
K. Berzins

SUMMARYCytoadherence ofPlasmodium falciparum-infected erythrocytes plays an important role in the pathogenesis of cerebral malaria. The identity of cell surface molecules on parasitized erythrocytes involved in cytoadherence is of great interest to understand the molecular basis of this mechanism. Peptide sequences derived from exofacial loops of the erythrocyte antigen band 3 from parasitized erythrocytes have previously been shown to inhibit cytoadherence. We now report that a non-repeated region of Pf155/RESA (residues 213–218) contains a hexapeptide motif being highly homologous to cytoadherence inhibitory sequences from band 3. Synthetic peptides containing the hexapeptide motif of Pf155/RESA inhibited the binding ofP.falciparum-infected erythrocytes to melanoma cellsin vitro. Furthermore, individuals residing in malaria-endemic areas have antibodies reactive with epitopes involving these motifs in band 3 and in Pf155/RESA.


2007 ◽  
Vol 172 ◽  
pp. S88
Author(s):  
Inge Nelissen ◽  
Geert R. Verheyen ◽  
Nathalie Lambrechts ◽  
Daniella Ooms ◽  
Hilde Leppens ◽  
...  

2004 ◽  
Vol 181 (3) ◽  
pp. 477-492 ◽  
Author(s):  
AA Fouladi Nashta ◽  
CV Andreu ◽  
N Nijjar ◽  
JK Heath ◽  
SJ Kimber

Decidualisation of uterine stromal cells is a prerequisite for implantation of the embryo in mice. Here we have used an in vitro culture system in which stromal cells decidualise as indicated by a number of markers, including an increase in alkaline phosphatase (ALP) activity. The latter was used as a quantitative marker of decidualisation in the presence of low (2%) fetal calf serum. Prostaglandin E(2) (PGE(2)), which is known to induce decidualisation, increased ALP activity, and this effect was blocked in a dose-dependent manner by indomethacin. Leukemia inhibitory factor (LIF) was then examined, but it had no effect on PGE(2) secretion. However, LIF suppressed ALP activity in a dose-dependent manner in the presence of 2% serum, while an inhibitor of LIF that competes for binding to its receptor reversed the effect of LIF and increased ALP activity above the control level. In serum-free cultures, stromal cells differentiated rapidly, and no differences were observed between LIF-treated and untreated cultures. Stromal cells produce LIF during in vitro culture, and this peaked at 48 h. Freshly collected stromal cells from both day-2 and -4 pregnant mice expressed mRNA for the LIF receptor, and the transcript level was higher in cells isolated on day 4. However, no differences were observed in the relative levels of transcripts in cells from day 2 and day 4 after culture, nor were there differences between the LIF-treated cultures and controls. Therefore, in this study, we have shown that LIF suppresses decidualisation of murine uterine stromal cells in the presence of serum, this is not due to the regulation of PGE(2) secretion by stromal cells.


1991 ◽  
Vol 266 (15) ◽  
pp. 9697-9702 ◽  
Author(s):  
A.H. Limper ◽  
B.J. Quade ◽  
R.M. LaChance ◽  
T.M. Birkenmeier ◽  
T.S. Rangwala ◽  
...  

Author(s):  
Abbas Ali Qayyum ◽  
Kamal Preet Kaur ◽  
Anders Bruun Mathiasen ◽  
Mandana Haack-Sørensen ◽  
Annette Ekblond ◽  
...  

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