scholarly journals Alkaline Phosphatase in Stem Cells

2015 ◽  
Vol 2015 ◽  
pp. 1-11 ◽  
Author(s):  
Kateřina Štefková ◽  
Jiřina Procházková ◽  
Jiří Pacherník

Alkaline phosphatase is an enzyme commonly expressed in almost all living organisms. In humans and other mammals, determinations of the expression and activity of alkaline phosphatase have frequently been used for cell determination in developmental studies and/or within clinical trials. Alkaline phosphatase also seems to be one of the key markers in the identification of pluripotent embryonic stem as well as related cells. However, alkaline phosphatases exist in some isoenzymes and isoforms, which have tissue specific expressions and functions. Here, the role of alkaline phosphatase as a stem cell marker is discussed in detail. First, we briefly summarize contemporary knowledge of mammalian alkaline phosphatases in general. Second, we focus on the known facts of its role in and potential significance for the identification of stem cells.

2021 ◽  
Vol 67 (3) ◽  
pp. 27-34
Author(s):  
D.I. Bilko ◽  
◽  
Y.B. Chaikovsky ◽  

Murine embryonic stem cells (ESCm) cultured in vitro in the presence of LIF (leukemia inhibitory factor) maintain pluripotency. However, when LIF is removed from the media, an active differentiation into various specialized somatic cells is observed. The aim of the study was to determine the role of substrate stiffness in maintaining of pluripotency of embryonic stem cells in vitro culture. To this aim, we used the method of culturing pluripotent stem cells in vitro, the method of “hanging drop”, the determination of the Young’s modulus for polyacrylamide gel of different hardness, the immunocytochemical alkaline phosphatase (AP) streptavidin-biotin method, microscopy. By culturing ESCm on a soft, medium and hard density polyacrylamide gel as a substrate (0.8, 4.0, 8.0 кPа), we found that on a soft gel ESCm differentiation does not occur even in the absence of LIF. ESCm cultured on a soft substrate continue to show signs of pluripotency, namely, create round compact colonies with high alkaline phosphatase activity and form embryoid bodies (EB), the efficiency of which (87.5 ± 3.2 per 100 cells seeded) did not decrease even after LIF withdrawal. In the absence of LIF, ESCs cultured on a hard base showed a low level of EB formation (23.5 ± 2.24). The results of our observations demonstrate that the process of EB formation may be influenced not only by a composition of nutrient medium, but also by complex interaction between the physical forces of the matrix and the mechanical properties of 3D cell aggregates. The model is considered as a tool to study early events in embryogenesis in the search of conditions for effective culture of progenitor cells and differentiated cells for transplantation.


1999 ◽  
Vol 27 (16) ◽  
pp. 3276-3282 ◽  
Author(s):  
P. P. H. Van Sloun ◽  
J. G. Jansen ◽  
G. Weeda ◽  
L. H. F. Mullenders ◽  
A. A. van Zeeland ◽  
...  

2021 ◽  
Vol 22 (2) ◽  
pp. 501
Author(s):  
Kateřina Skopalová ◽  
Katarzyna Anna Radaszkiewicz ◽  
Věra Kašpárková ◽  
Jaroslav Stejskal ◽  
Patrycja Bober ◽  
...  

The active role of biomaterials in the regeneration of tissues and their ability to modulate the behavior of stem cells in terms of their differentiation is highly advantageous. Here, polypyrrole, as a representantive of electro-conducting materials, is found to modulate the behavior of embryonic stem cells. Concretely, the aqueous extracts of polypyrrole induce neurogenesis within embryonic bodies formed from embryonic stem cells. This finding ledto an effort to determine the physiological cascade which is responsible for this effect. The polypyrrole modulates signaling pathways of Akt and ERK kinase through their phosphorylation. These effects are related to the presence of low-molecular-weight compounds present in aqueous polypyrrole extracts, determined by mass spectroscopy. The results show that consequences related to the modulation of stem cell differentiation must also be taken into account when polypyrrole is considered as a biomaterial.


2014 ◽  
Vol 237 (2) ◽  
pp. e8
Author(s):  
P. Gyambibi-Barnett ◽  
X. Yin ◽  
Y. Chung ◽  
A. Zampetaki ◽  
M. Mayr

Stem Cells ◽  
2009 ◽  
Vol 27 (9) ◽  
pp. 2092-2102 ◽  
Author(s):  
Eva Szabo ◽  
Tianshu Feng ◽  
Ewa Dziak ◽  
Michal Opas

2011 ◽  
Vol 57 (4) ◽  
pp. 356-361
Author(s):  
Ikuo Nishigaki ◽  
Gowri Rangasamy Gunassekaran ◽  
Panjan Nagappan Venkatesan ◽  
Mandupal Chaco Sabu ◽  
Sabu Priya ◽  
...  

2016 ◽  
Vol 24 ◽  
pp. S92-S93
Author(s):  
Hiroshi Kohara ◽  
Jiyuan Liao ◽  
Shohei Miyamoto ◽  
Yoko Nagai ◽  
Tomotoshi Marumoto ◽  
...  

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