scholarly journals Expansive growth of two glioblastoma stem-like cell lines is mediated by bFGF and not by EGF

2013 ◽  
Vol 47 (4) ◽  
pp. 330-337 ◽  
Author(s):  
Neza Podergajs ◽  
Narve Brekka ◽  
Bernhard Radlwimmer ◽  
Christel Herold-Mende ◽  
Krishna M. Talasila ◽  
...  

Abstract Background. Patient-derived glioblastoma (GBM) stem-like cells (GSCs) represent a valuable model for basic and therapeutic research. GSCs are usually propagated in serum-free Neural Basal medium supplemented with bFGF and EGF. Yet, the exact influence of these growth factors on GSCs is still unclear. Recently it was suggested that GBM stemlike cells with amplified EGFR should be cultured in stem cell medium without EGF, as the presence of EGF induced rapid loss of EGFR amplification. However, patient biopsies are usually taken into culture before their genomic profiles are defined. Thus, an important question remains whether GBM cells without EGFR amplification also can be cultured in stem cell medium without EGF. Meterials and methods. To address this question, we used two heterogeneous glioblastoma GSC lines (NCH421k and NCH644) that lack EGFR amplification. Results. Although both cell lines showed very low EGFR expression under standard growth conditions, bFGF stimulation induced higher expression of EGFR in NCH644. In both cell lines, expression of the stem cell markers nestin and CD133 was higher upon stimulation with bFGF compared to EGF. Importantly, bFGF stimulated the growth of both cell lines, whereas EGF had no effect. We verified that the growth stimulation by bFGF was either mediated by proliferation (NCH421k) or resistance to apoptosis (NCH644). Conclusions. We demonstrate that GSC cultures without EGFR amplification can be maintained and expanded with bFGF, while the addition of EGF has no significant effect and therefore can be omitted.

2017 ◽  
Author(s):  
George P. Albaugh ◽  
Sudhir K. Dutta ◽  
Vasantha Iyengar ◽  
Samina Shami ◽  
Althaf Lohani ◽  
...  

ABSTRACTUnderstanding the nature of cell surface markers on exfoliated colonic cells is a crucial step in establishing criteria for a normally functioning mucosa. We have found that colonic cells isolated from stool samples (SCSR-010 Fecal Cell Isolation Kit, NonInvasive Technologies, Elkridge, MD), preserved at room temperature for up to one week, with viability of >85% and low levels of apoptosis (8% - 10%) exhibit two distinct cell size subpopulations, in the 2.5μM– 5.0 μM and 5.0μM-8.0μM range. In addition to IgA, about 60% of the cells expressed a novel heterodimeric IgA/IgG immunoglobulin that conferred a broad-spectrum cell mediated cytotoxicity against tumor cells. In a cohort of 58 subjects the exclusive absence of this immunoglobulin in two African-Americans was suggestive of a germline deletion. Serial cultures in stem cell medium retained the expression of this heterodimer. Since a majority of the cystic cells expressed the stem cell markers Lgr5 and Musashi-1 we termed these cells as gastrointestinal progenitor stem cells (GIP-C**). CXCR-4, the cytokine co-receptor for HIV was markedly expressed. These cells also expressed CD20, IgA, IgG, CD45, and COX-2. We assume that they originated from mature columnar epithelium by dedifferentiation. Our observations indicate that we have a robust noninvasive method to study mucosal pathophysiology and a direct method to create a database for applications in regenerative medicine.


2021 ◽  
Vol 11 ◽  
Author(s):  
Lisa Wieland ◽  
Kristina Engel ◽  
Ines Volkmer ◽  
Anna Krüger ◽  
Guido Posern ◽  
...  

Neuroblastoma (NB) is the commonest solid tumor outside the central nervous system in infancy and childhood with a unique biological heterogeneity. In patients with advanced, metastasizing neuroblastoma, treatment failure and poor prognosis is often marked by resistance to chemo- or immunotherapy. Thus, identification of robust biomarkers seems essential for understanding tumor progression and developing effective therapy. Here, we have studied the expression of human endogenous retroviruses (HERV) as potential targets in NB cell lines during stem-cell medium-induced microenvironmental change. Quantitative PCR revealed that relative expression of the HERV-K family and HERV-W1 ENV were increased in all three NB cell lines after incubation in stem-cell medium. Virus transcriptome analyses revealed the transcriptional activation of three endogenous retrovirus elements: HERV-R ENV (ERV3-1), HERV-E1 and HERV-Fc2 ENV (ERVFC1-1). Known malignancy markers in NB, e.g. proto-oncogenic MYC or MYCN were expressed highly heterogeneously in the three investigated NB cell lines with up-regulation of MYC and MYCN upon medium-induced microenvironmental change. In addition, SiMa cells exclusively showed a phenotype switching from loosely-adherent monolayers to low proliferating grape-like cellular aggregates, which was accompanied by an enhanced CD133 expression. Interestingly, the overexpression of HERV was associated with a significant elevation of immune checkpoint molecule CD200 in both quantitative PCR and RNA-seq analysis suggesting tumor escape mechanism in NB cell lines after incubation in serum-free stem cell medium.


2010 ◽  
Vol 22 (1) ◽  
pp. 355
Author(s):  
M. A. Rasmussen ◽  
V. J. Hall ◽  
P. Hyttel

The use of neural stem cells (NSC) has gained increased attention as a means of treating neurodegenerative diseases such as Alzheimer’s and Parkinson’s disease. However, before regenerative treatment of humans can be undertaken, safety studies of NSC using animal models are required. The mouse has been the model of choice so far; however, testing in larger mammals such as the pig is essential. The aim of this study was to derive NSC from porcine epiblast cells and to analyze these cells using neural stem cell markers. A total of 47 epiblasts were isolated from E9 porcine embryos and grown on mouse embryonic fibroblast cells in a porcine embryonic stem cell medium. After 5 days, 23 outgrowth colonies had formed (49%). Based on morphology, 8 outgrowth colonies were selected and cut into 63 smaller pieces, which were transferred to MS5 stromal cells in a serum replacement medium, and after an additional 12 days, rosette structures had formed. These structures were transferred to Matrigel-coated dishes in a neural stem cell medium containing EGF and FGF. Under such conditions, bipolar cells containing large nuclei and several nucleoli grew out from the rosettes. The bipolar cells have been expanded for more than 8 passages without any change in morphology or growth rate, and upon high-density culture, the cells spontaneously form floating neurospheres. Stainings revealed that the cells expressed the neural stem cell markers Nestin (100%), Sox2 (100%), Pax6 (100%), and Vimentin (100%), as well as the proliferation marker Ki67 (54%). The same markers were found to be expressed in the lateral ventricles of the developing porcine brain, a location known to have high neurogenic activity. When growth factors were withdrawn from the culture medium, a higher proportion of TujI expressing cells were observed, especially when cells were cultured as neurospheres. We conclude that it is possible to derive presumptive NSC from porcine epiblast cells and that these express the same markers as reported for human NSC. Further studies are required to determine if the cells can be cultured long term and differentiate into various neuronal and glial cell types.


2015 ◽  
Vol 27 (1) ◽  
pp. 259
Author(s):  
T. Tharasanit ◽  
N. Tiptanavattana ◽  
P. Phakdeedindan ◽  
M. Techakumphu

Embryonic stem (ES) cells are pluripotent cells that can differentiate into all 3 germ layers, including endoderm, mesoderm, and ectoderm. Embryonic stem cells are generally divided into 2 types, naïve and primed-state, depending on their signaling pathways. Domestic cat is a useful animal model for the study of human diseases because many genetic and infectious diseases in the cat are analogous with similar aetiology to human diseases. The cat can also be used as a research model for reproductive physiology and conservation of wild felids. Until recently, information on establishment of feline ES cells is limited. The objectives of this study were to isolate cat ES cells from in vitro-produced blastocysts and to examine the effect of different concentrations of basic fibroblast growth factor (bFGF) on the expression of pluripotent genes. Inner cell masses (ICM) from cat blastocysts (n = 40, Day 7 after in vitro fertilization) that were matured, fertilized, and cultured entirely in vitro, were isolated by immunosurgery and plated on mitmycin-treated mouse embryonic fibroblasts. The ICM (n = 20) were then cultured in embryonic stem cell medium containing 1000 IU mL–1 of leukemia inhibitory factor (LIF) and different bFGF concentrations (0, 4, 10, and 20 ng mL–1). The ICM outgrowths at 7 days postplating were collected and analysed for expression of pluripotent genes (SOX-2, OCT-4, and NANOG). Results showed that transcription levels of all 3 pluripotent genes were higher in ICM outgrowths cultured in 20 ng mL–1 of bFGF compared with the lower concentrations. For isolation of ES cells, ICM (n = 20) were cultured in embryonic stem cell medium supplemented with 1000 IU mL–1 of LIF and 20 ng mL–1 of bFGF due to the results obtained from the above experiment. Established ES cells were characterised by detecting alkaline phosphatase (AP) activity and expression of ES markers (SOX-2, OCT-4, SSEA-4) at protein level, and karyotyped at passage 20 and 40. In vitro differentiation into embryoid bodies (EB) was induced by the hanging drop technique, and EB samples (n = 5 for each time point) were tested for the expression of TTR, AFP, T (Bracyury), NKX2.5, MAP-2, and NESTIN genes at 0, 7, and 14 days of culture. A total of 3 ES-like cell lines were established with a typical ES morphology, such as a well-defined colony, a large nucleus to cytoplasm ratio with 1 to 2 prominent nucleoli. The 3 ES-like cell lines were passaged up to 40 times with a normal diploid karyotype (n = 38). They were strongly positive for AP, SOX-2, OCT-4, and SSEA-4. Following EB culture, cell aggregation and cystic-like structure were observed. The EB samples also expressed all differentiation markers. This study reports that feline ES-like cell lines can be generated from in vitro-produced feline blastocysts. The ES cell lines can be repeatedly passaged indicating self-renewal ability, and gene expression of the EB demonstrates cellular differentiation into all 3 germ layers.


2014 ◽  
Vol 45 (5) ◽  
pp. 1857-1866 ◽  
Author(s):  
YUSAKU WATANABE ◽  
KIYOSHI YOSHIMURA ◽  
KOICHI YOSHIKAWA ◽  
RYOICHI TSUNEDOMI ◽  
YOSHITARO SHINDO ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Laura L. Stafman ◽  
Adele P. Williams ◽  
Raoud Marayati ◽  
Jamie M. Aye ◽  
Hooper R. Markert ◽  
...  

Abstract Patient-derived xenografts (PDXs) provide an opportunity to evaluate the effects of therapies in an environment that more closely resembles the human condition than that seen with long-term passage cell lines. In the current studies, we investigated the effects of FAK inhibition on two neuroblastoma PDXs in vitro. Cells were treated with two small molecule inhibitors of FAK, PF-573,228 (PF) and 1,2,4,5-benzentetraamine tetrahydrochloride (Y15). Following FAK inhibition, cell survival and proliferation decreased significantly and cell cycle arrest was seen in both cell lines. Migration and invasion assays were used to determine the effect of FAK inhibition on cell motility, which decreased significantly in both cell lines in the presence of either inhibitor. Finally, tumor cell stemness following FAK inhibition was evaluated with extreme limiting dilution assays as well as with immunoblotting and quantitative real-time PCR for the expression of stem cell markers. FAK inhibition decreased formation of tumorspheres and resulted in a corresponding decrease in established stem cell markers. FAK inhibition decreased many characteristics of the malignant phenotype, including cancer stem cell like features in neuroblastoma PDXs, making FAK a candidate for further investigation as a potential target for neuroblastoma therapy.


2013 ◽  
Vol 73 (7) ◽  
pp. 2368-2378 ◽  
Author(s):  
Amanda F. Swindall ◽  
Angelina I. Londoño-Joshi ◽  
Matthew J. Schultz ◽  
Naomi Fineberg ◽  
Donald J. Buchsbaum ◽  
...  

Zygote ◽  
2015 ◽  
Vol 24 (2) ◽  
pp. 236-244 ◽  
Author(s):  
Qing-Shan Gao ◽  
Long Jin ◽  
Suo Li ◽  
Hai-Ying Zhu ◽  
Qing Guo ◽  
...  

SummaryWe investigated the effect of human induced pluripotent stem cell (hiPS) medium on porcine somatic cell nuclear transfer and bovine in vitro fertilized early blastocysts, in comparison with North Carolina State University (NCSU)-37 medium and in vitro culture (IVC)-II medium. After 2 days of culture, the diameter of the portion of the blastocyst that was extruded from the zona pellucid dramatically differed between porcine blastocysts cultured in hiPS medium and those cultured in NCSU-37 medium (221.47 ± 38.94 μm versus 481.87 ± 40.61 μm, P < 0.01). Moreover, the diameter of the portion of the blastocyst significantly differed between bovine blastocysts cultured in hiPS medium and those cultured in IVC-II medium (150.30 ± 29.49 μm versus 195.58 ± 41.59 μm, P < 0.01). Furthermore, the total number of cells per porcine and bovine blastocyst was more than two-fold higher in blastocysts cultured in hiPS medium than in those cultured in NCSU-37 medium (44.33 ± 5.28 and 143.33 ± 16.05, P < 0.01) or IVC-II medium (172.12 ± 45.08 and 604.83 ± 242.64, P < 0.01), respectively. These results indicate that hiPS medium markedly improves the quality of porcine and bovine blastocysts.


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