Biochemical Pathways and Myometrial Cell Differentiation Leading to Nodule Formation Containing Collagen and Fibronectin

2016 ◽  
Vol 18 (2) ◽  
pp. 155-166 ◽  
Author(s):  
Liping Feng ◽  
Friederike Jayes ◽  
Lauren Johnson ◽  
David Schomberg ◽  
Phyllis Leppert
2021 ◽  
Author(s):  
Francine Lorencetti Silva ◽  
Giuliana Campos Chaves Lamarque ◽  
Fernanda Maria Machado Pereira Cabral de Oliveira ◽  
Paulo Nelson-Filho ◽  
Léa Assed Bezerra Silva ◽  
...  

Abstract Background: Leukotriene B4 (LTB4) is a potent lipid mediator that stimulate the immune response. Because dental pulp inflammation and dentin repair are intrinsically related responses, the aim of this research was to investigate the potential of LTB4 in inducing differentiation of dental pulp stem cells. Methods: Microspheres (MS) loaded with LTB4 were prepared using an oil emulsion solvent extraction evaporation process and sterility, characterization, efficiency of LTB4 encapsulation and in vitro LTB4 release assay were investigated. Mouse dental pulp stem cells (OD-21) were stimulated with soluble LTB4 or MS loaded with LTB4 (0.01 and 0.1 μM). Cytotoxicity and cell viability was determined by lactate dehydrogenase (LDH) and MTT (methylthiazol tetrazolium) assays . Gene expression were measured by quantitative reverse transcription polymerase chain reaction (qRT-PCR) after 3, 6, 24, 48 and 72 h. Results: Mineralized nodule formation was assessed after 28 days of OD-21 cell stimulation with LTB4. Groups were compared using the one-way ANOVA test followed by Dunnett's post-test (α = 0.05). Treatment with LTB4 or MS loaded with LTB4 (0.01 and 0.1 micrometer- μM) were not cytotoxic to OD-21 cells. Treatment with LTB4 modulated the expression of the Ibsp (integrin binding sialoprotein) and Runx2 (runt-related transcription factor 2) genes differently depending on the experimental period analyzed. Interestingly LTB4 loaded in microspheres (0.1 μM) allowed long term dental pulp cell differentiation and biomineralization. LTB4 loaded in MS was not cytotoxic and induced an odontoblastic cell phenotype differentiation. Conclusion: These findings shed light on a novel pharmacological strategy to induce dental pulp cell differentiation.


Author(s):  
H. Alasam

The possibility that intrathymic T-cell differentiation involves stem cell-lymphoid interactions in embryos led us to study the ultrastructure of epithelial cell in normal embryonic thymus. Studies in adult thymus showed that it produces several peptides that induce T-cell differentiation. Several of them have been chemically characterized, such as thymosin α 1, thymopoietin, thymic humoral factor or the serum thymic factor. It was suggested that most of these factors are secreted by populations of A and B-epithelial cells.Embryonic materials were obtained from inbred matings of Swiss Albino mice. Thymuses were disected from embryos 17 days old and prepared for transmission electron microscopy. Our studies showed that embryonic thymus at this stage contains undifferentiated and differentiated epithelial cells, large lymphoblasts, medium and few small lymphocytes (Fig. 5). No differences were found between cortical and medullary epithelial cells, in contrast to the findings of Van Vliet et al,. Epithelial cells were mostly of the A-type with low electron density in both cytoplasm and nucleus. However few B-type with high electron density were also found (Fig. 7).


2001 ◽  
Vol 120 (5) ◽  
pp. A517-A517
Author(s):  
A MIZOGUCHI ◽  
E MIZOGUCHI ◽  
Y DEJONG ◽  
H TAKEDATSU ◽  
F PREFFER ◽  
...  

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