Adli Mazhar, Parlak Mahmut, Li Yuwen, El-Dahr Samir S
Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virgina.
J Cell Biochem. 2015 Jun;116(6):893-902. doi: 10.1002/jcb.25048.
In mammals, formation of new nephrons ends perinatally due to consumption of mesenchymal progenitor cells. Premature depletion of progenitors due to prematurity or postnatal loss of nephrons due to injury causes chronic kidney disease and hypertension. Intensive efforts are currently invested in designing regenerative strategies to form new nephron progenitors from pluripotent cells, which upon further differentiation provide a potential source of new nephrons. To know if reprogramed renal cells can maintain their identity and fate requires knowledge of the epigenetic states of native nephron progenitors and their progeny. In this article, we summarize current knowledge and gaps in the epigenomic landscape of the developing kidney. We now know that Pax2/PTIP/H3K4 methyltransferase activity provides the initial epigenetic specification signal to the metanephric mesenchyme. During nephrogenesis, the cap mesenchyme housing nephron progenitors is enriched in bivalent chromatin marks; as tubulogenesis proceeds, the tubular epithelium acquires H3K79me2. The latter mark is uniquely induced during epithelial differentiation. Analysis of histone landscapes in clonal metanephric mesenchyme cell lines and in Wilms tumor and normal fetal kidney has revealed that promoters of poised nephrogenesis genes carry bivalent histone signatures in progenitors. Differentiation or stimulation of Wnt signaling promotes resolution of bivalency; this does not occur in Wilms tumor cells consistent with their developmental arrest. The use of small cell number ChIP-Seq should facilitate the characterization of the chromatin landscape of the metanephric mesenchyme and various nephron compartments during nephrogenesis. Only then we will know if stem and somatic cell reprogramming into kidney progenitors recapitulates normal development.
在哺乳动物中,由于间充质祖细胞的消耗,新肾单位的形成在围产期结束。由于早产导致祖细胞过早耗竭或因损伤导致出生后肾单位丢失会引发慢性肾病和高血压。目前,人们正在大力投入设计再生策略,以从多能细胞中形成新的肾单位祖细胞,这些祖细胞进一步分化后可成为新肾单位的潜在来源。要了解重编程的肾细胞是否能维持其身份和命运,需要了解天然肾单位祖细胞及其后代的表观遗传状态。在本文中,我们总结了发育中肾脏表观基因组格局的现有知识和空白。我们现在知道,Pax2/PTIP/H3K4甲基转移酶活性为后肾间充质提供了初始的表观遗传特异性信号。在肾发生过程中,容纳肾单位祖细胞的帽状间充质富含二价染色质标记;随着肾小管形成的进行,肾小管上皮获得H3K79me2。后一种标记是上皮分化过程中独特诱导产生的。对克隆的后肾间充质细胞系、肾母细胞瘤和正常胎儿肾脏中的组蛋白格局分析表明,处于准备状态的肾发生基因的启动子在祖细胞中携带二价组蛋白特征。Wnt信号的分化或刺激促进二价性的消退;这在肾母细胞瘤细胞中不会发生,这与它们的发育停滞一致。使用少量细胞的ChIP-Seq应该有助于表征肾发生过程中后肾间充质和各种肾单位区室的染色质格局。只有到那时,我们才会知道将干细胞和体细胞重编程为肾祖细胞是否能重现正常发育过程。