Showing 6 results for Differentiation
Ahmadi, Moosavi, Hosseinpour Feizi,
Volume 13, Issue 3 (9-2010)
Abstract
Background: Recently, reports have been made of the effects of boric acid (BA) on cancer prevention and inhibition of cancer cell proliferation. This study was designed to investigate the effects of this compound on K562 cell line as a model of chronic myeloid leukemia (CML). Materials and Methods: In this experimental trial, K562 cell line was cultured in the presence of 0.75 to 12 mmol concentrations of boric acid for 24, 48, 72, and 96 hour intervals. Anti-proliferative and cytotoxic effects of BA were measured by trypan blue exclusion test and MTT assay, respectively. Flow-cytometery was utilized for evaluating the effects of BA on cell cycle. Wright-giemsa staining was used for determining the effects of BA, and latex phagocytic assay was used for evaluating the phagocytic potential of the differentiated cells. Results: BA induced growth inhibition of K562 cells in a dose and time dependent manner after 96 hours of treatment with 12 mmol BA, cell proliferation of K562 cells was inhibited to about 83% (p<0.001). In addition, BA induced G1 cell cycle arrest in a way that for instance, after 6 days of treatment with 9 mmol BA, 98% of cell populations were at G1 level. Wright-giemsa staining and latex phagocytic assay results confirmed that K562 cells differentiated toward monocyte-macrophage lineage. Conclusion: Noticing the anti-proliferative and differentiating effects of BA, and no evidence of its adverse effects, this compound can be used as alone or in combination with other drugs in CML differentiation therapy.
Fatemeh Piryaei, Mina Ramezani, Fahimeh Piryaei,
Volume 14, Issue 2 (5-2011)
Abstract
Background: Noticing the practical significance of stem cells, this study was conducted to culture and screen bone marrow mesenchymal stem cells derived from Raf and Hilline chicken strains and investigate the effect of age and race on the morphology and differentiation of the generated cells.
Materials and Methods: In this fundamental study, bone marrow cells from 3 to 25 day-old Raf and Hiline chicken strains were cultured in low glucose DMEM, 10% BFS. Then third passage bone marrow cells of the two strains were compared in terms of morphology, differentiation to bone, cartilage, and adiposity. Data were analyzed through SPSS software.
Results: In culturing Raf chicken derived bone marrow cells, in contrast to Hiline chicken strain, colonization took place and they almost had a better fibroblastic morphology. The results indicated higher yields of differentiation to bone, cartilage, and adipose tissues in Raf chicken derived bone marrow cells than Hiline chicken. These differences were statistically significant. Also, 15 days was the most suitable age for screening the mesenchymal stem cells of chicken.
Conclusion: Screening and proliferation of mesenchymal stem cells from 15-day old Raf chicken bone marrow cells are good resources for differentiation and purification of chicken bone marrow mesenchymal stem cells.
Sara Sadegh Moghaddam Abaspour , Naser Mahdavi Shahri, Seyed Mohammad Ali Shariat Zadeh,
Volume 15, Issue 3 (8-2012)
Abstract
Background: Obtaining cells from the patient, expanding cell population on a scaffold, and, eventually, grafting the tissue to the patient is one of the tissue engineering techniques to create replacement tissue structures. Blastema tissue is one of the cellular sources in this regard. This study investigated the use of human gum tissue to prepare a scaffold and the interaction between the three-dimensional tissue scaffold and blastema tissue. Materials and Methods: In this experimental study, human gingiva was prepared and through snap freezing method and the use of sodium dodecyl sulfate (SDS) and Triton X-100, went through cell bleaching. Then the provided scaffoldings were placed in 2-day-old blastema rings and stored in culture media for 25 days. Sampling of the blastema and scaffolding tissues was done once every five days. Results: The results confirmed the removal of the cells from the prepared scaffolds. Also, histological studies in the fifth and tenth days indicated cell penetration into the blastema scaffolds. In the fifteenth day, in addition to penetration, blastema cells division and differentiation as well as epidermis genesis were observed. In the twentieth and twenty-fifth days, infiltration, cell division, and differentiation processes continued. Conclusion: The findings of this study indicated the possibility of creating a natural scaffold of human gingiva through this method. This scaffold can have an inductive effect on cell behaviors such as such as migration, adhesion, division, and probable differentiation. However, further studies for demonstrating the identity of the cells and other properties of such a scaffold as well as the possibility of using it in gingiva tissue engineering are recommended.
Mohammad Mosleh Abadi Farahani, Naser Amirizadeh, Arezoo Odi, Mona Khorshidfar, Mahin Nikougoftar Zarif,
Volume 17, Issue 7 (10-2014)
Abstract
Background: Hematopoietic stem cell transplants are routinely used to treat patients with cancers and other disorders of blood and immune systems. Osteoblasts constitute part of the stromal cell support system in marrow for hematopoiesis by participating in the formation of the HSC niche. It is believed that interaction between hematopoietic cells and bone forming osteoblasts regulate each other’s function. It is established that acute blood loss in animal models activates bone formation and niche development because of EPO stimulation. In this experimental study we have examined the co-culture of HSCs derived from cord blood which treated with EPO in vitro, on osteoblastic differentiation of mesenchymal stem cells.
Materials and Methods: In this experimental study MSCs isolated from bone marrow and co-cultured with CD 34+ CD38- HSCs isolated from cord blood. These co-cultured cells were treated with different doses of erythropoietin for 14 days, after that RNA were extracted from MSCs and analysed with RT-PCR to evaluate the expression of osteopontin and osteocalcin. Alizarin red and alkaline phosphatase staining were done for osteoblastic differentiation.
Results: Osteopontin and osteocalcin were expressed in MSCs. Cellular staining were positive for osteoblastic differentiation. Differentiated cells expressed osteoblastic markers.
Conclusion: These data suggest that EPO regulates the osteoblastic differentiation from bone marrow MSCs in vitro.
Homeyra Babaei, Javaher Chabavizadeh, Parvin Dehghan, Rasoul Mohammadi,
Volume 19, Issue 8 (11-2016)
Abstract
Abstract
Background: Candida albicans is still the main etiologic agent of candidiasis. However, infections of non-albicans Candida species are increasing. Candida dubliniensis is similar to C. albicans phenotypically and must be identified due to the better management of infection. The aim of the present study is to defferentiate and identify Candida species by Duplex PCR for getting an epidemiological data of Candida species among clinical specimens.
Materials and Methods: DNA was extracted using phenol-chloroform method from fresh colonies. Internal Transcribed Spacer region was amplified by polymerase chain reaction using specific primers. Based on differences of bands sizes on agarose gel electrophoresis, species were identified.
Results: Ninety four out of 100 patients (49 males and 51 females) had predisposing factors in the present study. Diabetes (73.4%), use of antibiotic (6.3%), vitamin deficiency (4.3%) were the main predisposing factors. The most specimens belonged to mouth (75%), vagina (5%), and blood (4%). All isolates were identified as C. albicans.
Conclusion: Duplex PCR is a rapid and precise method for the detection and differentiation of Candida species carefully, and in this method, phenotypic tests like germ-tube and chlamydoconidia production, as well as biochemical tests are not required for clinical laboratories that have limited resources and time for response to the patients, and it can replace with the traditional methods.
Mohsen Khaki, Hamid Abtahi, Ghasem Mosayebi,
Volume 22, Issue 6 (1-2020)
Abstract
Background and Aim: The most important problem in the production of recombinant proteins in prokaryotic cells is the disruption of the function of these proteins due to their altered natural structure. The aim of present study is to identify the best chemicals dialysis buffer additives in order to improve the protein structure of recombinant Vascular Endothelial Growth Factor (VEGF)
Methods & Materials: In this experimental study, different chemicals additives were selected using relevant software. After adding these additives to the recombinant VEGF dialysis buffer, their effect on the refolding of recombinant proteins and the differentiation of mesenchymal stem cells into endothelial cells was assessed by flow cytometry method.
Ethical Considerations: This study obtained its ethical approval from the Research Ethics Committee of Arak University of Medical Sciences (Code: ARAKMU. REC.1394.199).
Results: The results showed that the addition of arginine, cysteine and dithiothreitol (DTT) to dialysis buffer increases the differentiation of mesenchymal stem cells into endothelial cells. With the presence of sodium chloride (NaCl), cysteine, arginine and DTT in treated cells, the rate of specific Cluster Differentiation (CD) markers of endothelial cell (CD31/144) was at the highest level.
Conclusion: Adding cysteine, arginine, DTT and NaCl to the dialysis buffer of recombinant VEGF had the greatest effect on the mesenchymal cell differentiation into endothelial cells.
