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Relevant bibliographies by topics / Cultivated fibroblasts

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Journal articles

Academic literature on the topic 'Cultivated fibroblasts'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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Journal articles on the topic "Cultivated fibroblasts"

1

Pigeolet, E., M. Raes, A. Houbion, and J. Remacle. "Effect of procaine on cultivated human WI-38 fibroblasts." Experimental Gerontology 23, no. 2 (1988): 87–96. http://dx.doi.org/10.1016/0531-5565(88)90073-3.

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2

Levina, Elina M., Margarita A. Kharitonova, Yuri A. Rovensky, and Jury M. Vasiliev. "Cytoskeletal control of fibroblast length: experiments with linear strips of substrate." Journal of Cell Science 114, no. 23 (2001): 4335–41. http://dx.doi.org/10.1242/jcs.114.23.4335.

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In order to understand the factors determining the length of fibroblasts, three cell lines (mouse embryonic fibroblasts plus human fibroblast lines AGO 1523 and M19) were cultivated on the usual planar substrate (glass) and on specially prepared narrow linear strips of the same substrate, where the cells could spread only linearly. Morphometric measurements showed that the average length of cells of each type on the ‘unidimensional’ strips was no different from that on the usual ‘bidimensional’ substrate. The addition of colcemid significantly decreased cell length on both substrates, whereas

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3

Tansaz, Samira, Raminder Singh, Iwona Cicha, and Aldo Boccaccini. "Soy Protein-Based Composite Hydrogels: Physico-Chemical Characterization and In Vitro Cytocompatibility." Polymers 10, no. 10 (2018): 1159. http://dx.doi.org/10.3390/polym10101159.

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Novel composite hydrogels based on the combination of alginate (Alg), soy protein isolate (SPI) and bioactive glass (BG) nanoparticles were developed for soft tissue engineering. Human umbilical vein endothelial cells (HUVEC) and normal human dermal fibroblasts were cultivated on hydrogels for 7, 14 and 21 days. Cell morphology was visualized using fluorescent staining at Days 7 and 14 for fibroblast cells and Days 14 and 21 for HUVEC. Metabolic activity of cells was analyzed using a colorimetric assay (water soluble tetrazolium (WST) assay). Compared to pure Alg, Alg/SPI and Alg/SPI/BG provid

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4

Bongenhielm, U., A. Hægerstrand, E. Theodorsson, and K. Fried. "Effects of neuropeptides on growth of cultivated rat molar pulp fibroblasts." Regulatory Peptides 60, no. 2-3 (1995): 91–98. http://dx.doi.org/10.1016/0167-0115(95)00115-8.

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5

Doillon, Charles J., Arthur J. Wasserman, Richard A. Berg, and Frederick H. Silver. "Behaviour of fibroblasts and epidermal cells cultivated on analogues of extracellular matrix." Biomaterials 9, no. 1 (1988): 91–96. http://dx.doi.org/10.1016/0142-9612(88)90077-4.

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6

Letsiou, Sophia, Artemis Bakea, Géraldine Le Goff, et al. "Marine Fungus Aspergillus chevalieri TM2-S6 Extract Protects Skin Fibroblasts from Oxidative Stress." Marine Drugs 18, no. 9 (2020): 460. http://dx.doi.org/10.3390/md18090460.

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The strain Aspergillus chevalieri TM2-S6 was isolated from the sponge Axinella and identified according to internal transcribed spacer (ITS) molecular sequence homology with Aspergillus species from the section Restricti. The strain was cultivated 9 days on potato dextrose broth (PDB), and the medium evaluated as antioxidant on primary normal human dermal fibroblasts (NHDF). The cultivation broth was submitted to sterile filtration, lyophilized and used without any further processing to give the Aspergillus chevalieri TM2-S6 cultivation broth ingredient named ACBB. ACCB contains two main compo

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7

Bonatti, Silvilena, Bernardo Hochman, Vanina Monique Tucci-Viegas, et al. "In vitro effect of 470 nm LED (Light Emitting Diode) in keloid fibroblasts." Acta Cirurgica Brasileira 26, no. 1 (2011): 25–30. http://dx.doi.org/10.1590/s0102-86502011000100006.

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Purpose: To quantify keloid fibroblasts after irradiation with 470nm blue LED, in vitro. Methods: Fibroblasts from keloid and adjacent skin have been obtained from 6 patients. Cells have been cultivated and maintained in DMEM culture medium. In Petri dishes, they were irradiated with energy doses of 6J, 12J and 18J. After 24 h, counting was done by the average of the triplicates for each sample. Results: There were no significant differences in the number of irradiated keloid fibroblasts at the studied doses (p=0.261). In adjacent skin fibroblasts, differences were observed (p=0.025) concernin

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8

Yartsev, Vasily, Anna Gabashvili, Eugenia Atkova, Pavel Melnikov, and Tatiana Nesterova. "Study of Dosage-Dependent Effects of Cytostatic Drugs Using a Fibroblast Cell Culture of the Human Nasal Mucosa." International Archives of Otorhinolaryngology 24, no. 02 (2020): e206-e210. http://dx.doi.org/10.1055/s-0039-1697996.

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Abstract Introduction Knowing a concentration at which cytostatic drugs are toxic for the nasal fibroblasts will enable the use cytostatic drugs in the clinical practice to prevent excessive cicatrization. Objective To determine the cytostatic concentrations of mitomycin С, doxorubicin, and 5-fluorouracil affecting nasal mucosa fibroblasts. Methods We obtained material during an endonasal dacryocystorhinostomy with the patient's informed consent. The cells were cultivated. Second- to fourth-passage cells were used in the experiments. The cells were stained for vimentin and cluster of different

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9

Van Gansen, Paulette, and Nadine Van Lerberghe. "Potential and limitations of cultivated fibroblasts in the study of senescence in animals. A review on the murine skin fibroblasts system." Archives of Gerontology and Geriatrics 7, no. 1 (1988): 31–74. http://dx.doi.org/10.1016/0167-4943(88)90021-0.

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10

Markhoff, Jana, Martin Krogull, Christian Schulze, Christian Rotsch, Sandra Hunger, and Rainer Bader. "Biocompatibility and Inflammatory Potential of Titanium Alloys Cultivated with Human Osteoblasts, Fibroblasts and Macrophages." Materials 10, no. 1 (2017): 52. http://dx.doi.org/10.3390/ma10010052.

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