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Expression pattern of histone H3 subtypes in articular chondrocytes

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Three-dimensional cell culture used for tissue engineering has its own rules and directions. There is a deficiency of proliferative markers suitable for tissue engineering research when cells are cross-linked in network of fibers or suspended in hydrogel. It limits cell harvesting or impairs the flow to cell area conventional chemicals used as proliferative markers. According to current published data, the expression of replication-dependent histone H3 genes could be novel proliferative marker of cells. The intensive synthesis of H3 histones is tightly correlated with DNA synthesis and H3 mRNA is rapidly degraded when the S phase is completed or inhibited by cell cycle inhibitors. Based on this relation, non-dividing cells contain no H3 mRNA. The aim of the study was to determine expression pattern of replication-dependent H3 subtypes and tissue-specific H3/t subtype in normal human connective tissue cells. Analyzed cellular model was chondrocytes cell line due to the phenomenon that articular cartilage doesn't have natural ability to heal its injuries, consequently development of cartilage engineering is necessary. Evaluation of expression pattern was performed using Reverse Transcription PCR and reaction products were visualized on the gel electrophoresis. This study demonstrated that RT-PCR technique can be successfully used to study the expression of different histone H3 subtypes. Presented electrophoregram showed differential expression of the analyzed subtypes (no expression of H3/g and H3/t subtypes). Incubation with sodium butyrate and quantitative Real Time PCR enabled quantification of mRNA level of selected H3/d subtype. This part of study showed a significant reduction in the mRNA level of H3/d when the sodium butyrate was added. Obtained results indicated the possibility of using the expression of individual histone H3 subtype as a new proliferative marker.
Rocznik
Strony
2--5
Opis fizyczny
Bibliogr. 17 poz., tab., wykr.
Twórcy
autor
  • Department of Biotechnology and Genetic Engineering, Medical University of Silesia, Narcyzów 1, 41-206 Sosnowiec, Poland
autor
  • Department of Molecular Biology, Medical University of Silesia, Narcyzów 1, 41-206 Sosnowiec, Poland
autor
  • Department of Biopharmacy, Medical University of Silesia, Narcyzów 1, 41-206 Sosnowiec, Poland
  • Department of Biopharmacy, Medical University of Silesia, Narcyzów 1, 41-206 Sosnowiec, Poland
autor
  • Department of Biotechnology and Genetic Engineering, Medical University of Silesia, Narcyzów 1, 41-206 Sosnowiec, Poland
Bibliografia
  • [1] Ikada Y.: Challenges in tissue engineering. J R Soc Interface 2006; 3(10): 589-601.
  • [2] Lin Z., Willers C., Xu J., Zheng M.H.: The chondrocyte: biology and clinical application. Tissue Eng 2006; 7(12): 1971-1984.
  • [3] Bosch F.X., Udvarhelyi N., Venter E., Herold-Mende C., Schuhmann A., Maier H., Weidauer H., Born A.I. Expression of the histone H3 gene in benign, semi-malignant and malignant lesions of the head and neck: a reliable proliferation marker. Eur J Cancer 1993; 29A(10): 1454-1461.
  • [4] Rautiainen E., Haapasalo H., Sallinen P., Rantala I., Helen P., Helin H.: Histone mRNA in-situ hybridization in astrocytomas: a comparison with PCNA, MIB-1 and mitoses in paraffin-embedded material. Histopathology 1998; 32(1): 43-50.
  • [5] Muskhelishvili L., Latendresse J.R., Kodell R.L., Henderson E.B.: Evaluation of cell proliferation in rat tissues with BrdU, PCNA, Ki-67(MIB-5) immunohistochemistry and in situ hybridization for histone mRNA. J Histochem Cytochem 2003; 51(12):1681-1688.
  • [6] Wong D.T.W., Chou M.Y., Chang L.C., Gallagher G.T.: Use of intracelluar H3 messenger RNA as a marker to determine the proliferation pattern of normal and 7,12-dimethylbenz[a]antracene- transformed hamster oral epithelium. Cancer Res 1990; 50(16): 5107-5111.
  • [7] Tian X., Xu J., Zhou H., Liu R., Chen J., Huang X.: Thr 3 phosphorylated histone H3 concentrates at centromeric chromatin at metaphase. Biochem Biophys Res Commun. 2010;401(4):618-23.
  • [8] Doenecke D., Albig W., Bode C., Drabent B., Franke K., Gavenis K., Witt O.: Histones: gene diversity and tissue-specific gene expression. Histochem Cell Biol 1997; 107: 1-10.
  • [9] Govin J., Caron C., Rousseaux S., Khochbin S.: Testis-specific histone H3 expression in somatic cells. Trends Biochem Sci. 2005; 30(7):357-359.
  • [10] Dominski Z., Marzluff W.F.: Formation of the 3' end of histone mRNA. Gene 1999;239: 1-14.
  • [11] Brock W.A., Trostle-Weige P.K., Williams M., Meistrich M.L.: Histone and DNA synthesis in differentiating and rapidly proliferating cells in vivo and in vitro. Cell Differ 1983; 12(1): 47-55
  • [12] Koh C.J., Atala A.: Tissue engineering, stem cells, and cloning: opportunities for regenerative medicine. J Am Soc Nephrol 2004; 15(5): 1113-1125.
  • [13] Slowinski J., Mazurek U., Bierzynska-Macyszyn G.: Histone mRNA In situ hybridization In assessing proliferative activity of normal and malignant cells. Folia Histochemica et Cytobiologica 2002 ; 40(4): 335-339.
  • [14] Chou M.Y., Chang A.L.C., McBride J., Donoff B., Gallagher G.T., Wong D.T.: A rapid method to determine proliferation patterns of normal and malignant tissues by H3 mRNA in situ hybridization. Am J Pathol 1990; 136: 729-733.
  • [15] Ignatius A., Blessing H., Liedert A., Schmidt C., Neidlinger-Wilke C., Kaspar D., Friemert B., Claes L.: Tissue engineering of bone: effects of mechanical strain on osteoblastic cells in type I collagen matrices. Biomaterials 2005; 26(3): 311-318.
  • [16] Koessler H., Doenecke D., Albig W.: Aberrant expression pattern of replication-dependent histone H3 subtype genes in human tumor cell lines. DNA and Cell Biology 2003; 22(4): 233-240.
  • [17] Koessler H., Kahle J., Bode C., Doenecke D., Albig W.: Human replication-dependent histone H3 genes are activated by a tandemly arranged pair of two CCAAT boxes. Biochem J 2004; 384(2): 317-326.
Uwagi
EN
This work was supported by the European Community from the European Social Fund within the RFSD 2 project and funded by the grant MEMSTENT (brand No:UDA-POIG.01.03.01-00-123/08-04) and KNW-1-030/D/1/0.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-7de49197-d17a-46a9-8aee-f27f5f29379c
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