scholarly journals Adenosine 3′,5′-Monophosphate in Glial Tumor Cells

1973 ◽  
Vol 248 (8) ◽  
pp. 2699-2704
Author(s):  
Joan P. Schwartz ◽  
N. Ronald Morris ◽  
Bruce McL. Breckenridge
Keyword(s):  
1976 ◽  
Vol 251 (15) ◽  
pp. 4744-4750 ◽  
Author(s):  
M A Brostrom ◽  
C O Brostrom ◽  
B M Breckenridge ◽  
D J Wolff

2013 ◽  
Vol 228 (7) ◽  
pp. 1383-1390 ◽  
Author(s):  
Ping-Pin Zheng ◽  
Marcel van der Weiden ◽  
Peter J. van der Spek ◽  
Arnaud J.P.E. Vincent ◽  
Johan M. Kros

1998 ◽  
Vol 79 (5) ◽  
pp. 2782-2793 ◽  
Author(s):  
Angélique Bordey ◽  
Harald Sontheimer

Bordey, Angélique and Harald Sontheimer. Electrophysiological properties of human astrocytic tumor cells in situ: enigma of spiking glial cells. J. Neurophysiol. 79: 2782–2793, 1998. To better understand physiological changes that accompany the neoplastic transition of astrocytes to become astrocytoma cells, we studied biopsies of low-grade, pilocytic astrocytomas. This group of tumors is most prevalent in children and the tumor cells maintain most antigenic features typical of astrocytes. Astrocytoma cells were studied with the use of whole cell patch-clamp recordings in acute biopsy slices from 4-mo- to 14-yr-old pediatric patients. Recordings from 53 cells in six cases of low-grade astrocytomas were compared to either noncancerous peritumoral astrocytes or astrocytes obtained from other surgeries. Astrocytoma cells almost exclusively displayed slowly activating, sustained, tetraethylammonium (TEA)-sensitive outward potassium currents (delayed rectifying potassium currents; I DR) and transient, tetrodotoxin (TTX)-sensitive sodium currents ( I Na). By contrast, comparison glial cells from peritumoral regions or other surgeries showed I DR and I Na, but in addition these cells also expressed transient “A”-type K+ currents and inwardly rectifying K+ currents ( I IR), both of which were absent in astrocytoma cells. I IR constituted the predominant conductance in comparison astrocytes and was responsible for a high-resting K+ conductance in these cells. Voltage-activated Na+ currents were observed in 37 of 53 astrocytoma cells. Na+ current densities in astrocytoma cells, on average, were three- to fivefold larger than in comparison astrocytes. Astrocytoma cells expressing I Na could be induced to generate slow action potential-like responses (spikes) by current injections. The threshold for generating such spikes was −34 mV (from a holding potential of −70 mV). The spike amplitude and time width were 52.5 mV and 12 ms, respectively. No spikes could be elicited in comparison astrocytes, although some of them expressed Na+ currents of similar size. Comparison of astrocytes to astrocytoma cells suggests that the apparent lack of I IR, which leads to high-input resistance (>500 MΩ), allows glioma cells to be sufficiently depolarized to generate Na+ spikes, whereas the high resting K+ conductance in astrocytes prevents their depolarization and thus generation of spikes. Consistent with this notion, Na+ spikes could be induced in spinal cord astrocytes in culture when I IR was experimentally blocked by 10 μM Ba2+, suggesting that the absence of I IR in astrocytoma cells is primarily responsible for the unusual spiking behavior seen in these glial tumor cells. It is unlikely that such glial spikes ever occur in vivo.


1987 ◽  
Vol 67 (6) ◽  
pp. 874-879 ◽  
Author(s):  
Thomas L. Roszman ◽  
William H. Brooks ◽  
Lucinda H. Elliott

✓ The results of this study demonstrate the presence of suppressive factor(s) in the tissue culture supernatants of cloned and freshly explanted malignant glioma cells. Culture supernatants obtained from these glial cell lines were demonstrated to have potent suppressive activity as evidenced by their ability to inhibit the proliferative response of normal human peripheral blood lymphocytes induced by phytohemagglutinin and anti-OKT3 monoclonal antibodies. The results further demonstrate the existence of a dose-response relationship between these supernatants and inhibition of mitogen-induced lymphocyte activation. Maximum production of suppressive activity by glial tumor cells was dependent on: 1) the number of tumor cells seeded in culture, 2) whether fetal calf serum was present, and 3) the duration of culture. The production of the suppressive factor(s) was not inhibited by the addition of inhibitors of prostaglandin E synthesis. Experiments designed to determine at what time during lymphocyte activation the suppressive factor was most effective demonstrated that the culture supernatants must be added during the first 24 hours of culture to exhibit inhibitory properties. Finally, proliferation of both the T-helper and T-suppressor/cytotoxic subsets was equally well inhibited by the glial tumor cell culture supernatants.


2020 ◽  
Vol 192 ◽  
pp. 111020 ◽  
Author(s):  
Marjana Radünz ◽  
Helen Cristina Dos Santos Hackbart ◽  
Natália Pontes Bona ◽  
Nathalia Stark Pedra ◽  
Jessica Fernanda Hoffmann ◽  
...  

1987 ◽  
Vol 46 (3) ◽  
pp. 371 ◽  
Author(s):  
F. Ali-Osman ◽  
J. Caughlin ◽  
M. Berger ◽  
A. Spence ◽  
Alexander Spence

1974 ◽  
Vol 86 (2) ◽  
pp. 425-428 ◽  
Author(s):  
B.P. Schimmer ◽  
Linda F. Stevenson ◽  
Cornelia Ter Hofstede ◽  
Ngai Hoi Cheung ◽  
A. Marks

2017 ◽  
Vol 19 (suppl_3) ◽  
pp. iii60-iii60
Author(s):  
J. M. Kros ◽  
K. Huizer ◽  
C. Zhu ◽  
C. Cheng ◽  
D. A. M. Mustafa
Keyword(s):  

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