KDM6B epigenetically regulates odontogenic differentiation of dental mesenchymal stem cells

Juan Xu , Bo Yu , Christine Hong , Cun-Yu Wang

International Journal of Oral Science ›› 2013, Vol. 5 ›› Issue (4) : 200 -205.

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International Journal of Oral Science ›› 2013, Vol. 5 ›› Issue (4) : 200 -205. DOI: 10.1038/ijos.2013.77
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KDM6B epigenetically regulates odontogenic differentiation of dental mesenchymal stem cells

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Abstract

A protein that regulates bone development may offer a useful target for promoting stem cell-mediated dental regeneration, report dental scientists in the US and China. The jaw contains multiple mesenchymal stem cell (MSC) populations that have the capacity to develop into a variety of mature cell types. Scientists see great potential in using these cells to repair dental damage, but they require a thorough understanding of how MSC’s development is coordinated. Christine Hong and Cun-Yu Wang of the University of California at Los Angeles have identified a protein that directly facilitates bone formation in dentally derived MSCs. They demonstrated that the enzyme KDM6B activates several genes that facilitate the transformation of MSCs into mature bone tissue. They also showed that this process is essentially blocked in the absence of KDM6B, confirming this protein’s critical role in stem cell based dental repair.

Keywords

bone morphogenic protein / dental mesenchymal stem cell / epigenetics / KDM6B / odontogenic differentiation

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Juan Xu, Bo Yu, Christine Hong, Cun-Yu Wang. KDM6B epigenetically regulates odontogenic differentiation of dental mesenchymal stem cells. International Journal of Oral Science, 2013, 5(4): 200-205 DOI:10.1038/ijos.2013.77

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References

[1]

Dominici M, Le Blanc K, Mueller I. Minimal criteria for defining multipotent mesenchymal stromal cells. The international society for cellular therapy position statement. Cytotherapy, 2006, 8(4): 315-317.

[2]

Kolf CM, Cho E, Tuan RS. Mesenchymal stromal cells. Biology of adult mesenchymal stem cells: regulation of niche, self-renewal and differentiation. Arthritis Res Ther, 2007, 9(1): 204.

[3]

Phinney DG, Prockop DJ. Concise review: mesenchymal stem/multipotent stromal cells: the state of transdifferentiation and modes of tissue repair—current views. Stem Cells, 2007, 25(11): 2896-2902.

[4]

Undale AH, Westendorf JJ, Yaszemski MJ. Mesenchymal stem cells for bone repair and metabolic bone diseases. Mayo Clin Proc, 2009, 84(10): 893-902.

[5]

Kuhn NZ, Tuan RS. Regulation of stemness and stem cell niche of mesenchymal stem cells: implications in tumorigenesis and metastasis. J Cell Physiol, 2010, 222(2): 268-277.

[6]

Fan Z, Yamaza T, Lee JS. BCOR regulates mesenchymal stem cell function by epigenetic mechanisms. Nat Cell Biol, 2009, 11(8): 1002-1009.

[7]

Chang J, Sonoyama W, Wang Z. Noncanonical Wnt-4 signaling enhances bone regeneration of mesenchymal stem cells in craniofacial defects through activation of p38 MAPK. J Biol Chem, 2007, 282(42): 30938-30948.

[8]

Jenuwein T, Allis CD. Translating the histone code. Science, 2001, 293(5532): 1074-1080.

[9]

Stein GS, van Wijnen AJ, Imbalzano AN. Architectural genetic and epigenetic control of regulatory networks: compartmentalizing machinery for transcription and chromatin remodeling in nuclear microenvironments. Crit Rev Eukaryot Gene Expr, 2010, 20(2): 149-155.

[10]

Agger K, Christensen J, Cloos PA. The emerging functions of histone demethylases. Curr Opin Genet Dev, 2008, 18(2): 159-168.

[11]

Klose RJ, Kallin EM, Zhang Y. JmjC-domain-containing proteins and histone demethylation. Nat Rev Genet, 2006, 7(9): 715-727.

[12]

Shi Y. Histone lysine demethylases: emerging roles in development, physiology and disease. Nat Rev Genet, 2007, 8(11): 829-833.

[13]

Sinha KM, Yasuda H, Coombes MM. Regulation of the osteoblast-specific transcription factor Osterix by NO66, a Jumonji family histone demethylase. EMBO J, 2010, 29(1): 68-79.

[14]

Ye L, Fan Z, Yu B. Histone demethylases KDM4B and KDM6B promotes osteogenic differentiation of human MSCs. Cell Stem Cell, 2012, 11(1): 50-61.

[15]

Lan F, Bayliss PE, Rinn JL. A histone H3 lysine 27 demethylase regulates animal posterior development. Nature, 2007, 449(7163): 689-694.

[16]

Akizu N, Estaras C, Guerrero L. H3K27me3 regulates BMP activity in developing spinal cord. Development, 2010, 137(17): 2915-2925.

[17]

Burgold T, Spreafico F, de Santa F. The histone H3 lysine 27-specific demethylase Jmjd3 is required for neural commitment. PloS ONE, 2008, 3(8): e3034.

[18]

Estaras C, Akizu N, Garcia A. Genome-wide analysis reveals that Smad3 and JMJD3 HDM co-activate the neural developmental program. Development, 2012, 139(15): 2681-2691.

[19]

Park BK, Zhang H, Zeng Q. NF-κB in breast cancer cells promotes osteolytic bone metastasis by inducing osteoclastogenesis via GM-CSF. Nat Med, 2007, 13(1): 62-69.

[20]

Huang GT, Gronthos S, Shi S. Mesenchymal stem cells derived from dental tissues vs. those from other sources: their biology and role in regenerative medicine. J Dent Res, 2009, 88(9): 792-806.

[21]

Vainio S, Karavanova I, Jowett A. Identification of BMP-4 as a signal mediating secondary induction between epithelial and mesenchymal tissues during early tooth development. Cell, 1993, 75(1): 45-58.

[22]

Nakashima M, Reddi AH. The application of bone morphogenetic proteins to dental tissue engineering. Nat Biotechnol, 2003, 21(9): 1025-1032.

[23]

Oh SH, Hwang YC, Yang H. SHP is involved in BMP2-induced odontoblast differentiation. J Dent Res, 2012, 91(12): 1124-1129.

[24]

De Santa F, Totaro MG, Prosperini E. The histone H3 lysine-27 demethylase Jmjd3 links inflammation to inhibition of polycomb-mediated gene silencing. Cell, 2007, 130(6): 1083-1094.

[25]

Noel D, Caton D, Roche S. Cell specific differences between human adipose-derived and mesenchymal-stromal cells despite similar differentiation potentials. Exp Cell Res, 2008, 314(7): 1575-1584.

[26]

Peng L, Dong G, Xu P. Expression of Wnt5a in tooth germs and the related signal transduction analysis. Arch Oral Biol, 2010, 55(2): 108-114.

[27]

Alge DL, Zhou D, Adams LL. Donor-matched comparison of dental pulp stem cells and bone marrow-derived mesenchymal stem cells in a rat model. J Tissue Eng Regen Med, 2010, 4(1): 73-81.

[28]

Six N, Lasfargues JJ, Goldberg M. Differential repair responses in the coronal and radicular areas of the exposed rat molar pulp induced by recombinant human bone morphogenetic protein 7 (osteogenic protein 1). Arch Oral Biol, 2002, 47(3): 177-187.

[29]

Yamashiro T, Tummers M, Thesleff I. Expression of bone morphogenetic proteins and Msx genes during root formation. J Dent Res, 2003, 82(3): 172-176.

[30]

Robinson GW, Mahon KA. Differential and overlapping expression domains of Dlx-2 and Dlx-3 suggest distinct roles for Distal-less homeobox genes in craniofacial development. Mech Dev, 1994, 48(3): 199-215.

[31]

Gordon CT, Brinas IM, Rodda FA. Role of Dlx genes in craniofacial morphogenesis: Dlx2 influences skeletal patterning by inducing ectomesenchymal aggregation in ovo. Evol Dev, 2010, 12(5): 459-473.

[32]

Lezot F, Thomas B, Hotton D. Biomineralization, life-time of odontogenic cells and differential expression of the two homeobox genes MSX-1 and DLX-2 in transgenic mice. J Bone Miner Res, 2000, 15(3): 430-441.

[33]

Peng L, Jia Z, Yin X. Comparative analysis of mesenchymal stem cells from bone marrow, cartilage, and adipose tissue. Stem Cells Dev, 2008, 17(4): 761-773.

[34]

McCollum M, Sharpe PT. Evolution and development of teeth. J Anat, 2001, 199(Pt 1/2): 153-159.

[35]

Thomas BL, Tucker AS, Qui M. Role of Dlx-1 and Dlx-2 genes in patterning of the murine dentition. Development, 1997, 124(23): 4811-4818.

[36]

Priam F, Ronco V, Locker M. New cellular models for tracking the odontoblast phenotype. Arch Oral Biol, 2005, 50(2): 271-277.

[37]

Hassan MQ, Javed A, Morasso MI. Dlx3 transcriptional regulation of osteoblast differentiation: temporal recruitment of Msx2, Dlx3, and Dlx5 homeodomain proteins to chromatin of the osteocalcin gene. Mol Cell Biol, 2004, 24(20): 9248-9261.

[38]

Hassan MQ, Tare RS, Lee SH. BMP2 commitment to the osteogenic lineage involves activation of Runx2 by DLX3 and a homeodomain transcriptional network. J Biol Chem, 2006, 281(52): 40515-40526.

[39]

Sen GL, Webster DE, Barragan DI. Control of differentiation in a self-renewing mammalian tissue by the histone demethylase JMJD3. Genes Dev, 2008, 22(14): 1865-1870.

[40]

Jiang W, Wang J, Zhang Y. Histone H3K27me3 demethylases KDM6A and KDM6B modulate definitive endoderm differentiation from human ESCs by regulating WNT signaling pathway. Cell Res, 2013, 23(1): 122-130.

[41]

Kartikasari AE, Zhou JX, Kanji MS. The histone demethylase Jmjd3 sequentially associates with the transcription factors Tbx3 and Eomes to drive endoderm differentiation. EMBO J, 2013, 32(10): 1393-1408.

[42]

Miller SA, Mohn SE, Weinmann AS. Jmjd3 and UTX play a demethylase-independent role in chromatin remodeling to regulate T-box family member-dependent gene expression. Mol Cell, 2010, 40(4): 594-605.

[43]

Tang Y, Wu X, Lei W. TGF-beta1-induced migration of bone mesenchymal stem cells couples bone resorption with formation. Nat Med, 2009, 15(7): 757-765.

[44]

Medici D, Shore EM, Lounev VY. Conversion of vascular endothelial cells into multipotent stem-like cells. Nat Med, 2010, 16(12): 1400-1406.

[45]

Kronenberg HM. Gs signaling in osteoblasts and hematopoietic stem cells. Ann NY Acad Sci, 2010, 1192: 327-329.

[46]

Huebsch N, Arany PR, Mao AS. Harnessing traction-mediated manipulation of the cell/matrix interface to control stem-cell fate. Nat Mater, 2010, 9(6): 518-526.

[47]

Yen AH, Sharpe PT. Regeneration of teeth using stem cell-based tissue engineering. Expert Opin Biol Ther, 2006, 6(1): 9-16.

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