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41.
Ludovic?Le Guen Stéphane?Marchal Sandrine?Faure Pascal?de Santa BarbaraEmail author 《Cellular and molecular life sciences : CMLS》2015,72(20):3883-3896
The gastrointestinal tract develops from a simple and uniform tube into a complex organ with specific differentiation patterns along the anterior–posterior and dorso-ventral axes of asymmetry. It is derived from all three germ layers and their cross-talk is important for the regulated development of fetal and adult gastrointestinal structures and organs. Signals from the adjacent mesoderm are essential for the morphogenesis of the overlying epithelium. These mesenchymal–epithelial interactions govern the development and regionalization of the different gastrointestinal epithelia and involve most of the key morphogens and signaling pathways, such as the Hedgehog, BMPs, Notch, WNT, HOX, SOX and FOXF cascades. Moreover, the mechanisms underlying mesenchyme differentiation into smooth muscle cells influence the regionalization of the gastrointestinal epithelium through interactions with the enteric nervous system. In the neonatal and adult gastrointestinal tract, mesenchymal–epithelial interactions are essential for the maintenance of the epithelial regionalization and digestive epithelial homeostasis. Disruption of these interactions is also associated with bowel dysfunction potentially leading to epithelial tumor development. In this review, we will discuss various aspects of the mesenchymal–epithelial interactions observed during digestive epithelium development and differentiation and also during epithelial stem cell regeneration. 相似文献
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43.
Beryl?Royer-Bertrand Carlo?RivoltaEmail author 《Cellular and molecular life sciences : CMLS》2015,72(8):1463-1471
The past decade has seen the emergence of next-generation sequencing (NGS) technologies, which have revolutionized the field of human molecular genetics. With NGS, significant portions of the human genome can now be assessed by direct sequence analysis, highlighting normal and pathological variants of our DNA. Recent advances have also allowed the sequencing of complete genomes, by a method referred to as whole genome sequencing (WGS). In this work, we review the use of WGS in medical genetics, with specific emphasis on the benefits and the disadvantages of this technique for detecting genomic alterations leading to Mendelian human diseases and to cancer. 相似文献
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[目的]针对协同训练算法在视图分割时未考虑噪声影响和两视图分类器对无标记样本标注不一致问题,提出了基于加权主成分分析和改进密度峰值聚类的协同训练算法.[方法]首先引入加权主成分分析对数据进行预处理,通过寻求初始有标记样本中特征和类标记之间的依赖关系求得各特征加权系数,再对加权变换后的数据进行降维并提取高贡献度特征进行视... 相似文献
46.
Gauthier LR Granotier C Hoffschir F Etienne O Ayouaz A Desmaze C Mailliet P Biard DS Boussin FD 《Cellular and molecular life sciences : CMLS》2012,69(4):629-640
Functional telomeres are protected from non-homologous end-joining (NHEJ) and homologous recombination (HR) DNA repair pathways.
Replication is a critical period for telomeres because of the requirement for reconstitution of functional protected telomere
conformations, a process that involves DNA repair proteins. Using knockdown of DNA-PKcs and Rad51 expression in three different
cell lines, we demonstrate the respective involvement of NHEJ and HR in the formation of telomere aberrations induced by the
G-quadruplex ligand 360A during or after replication. HR contributed to specific chromatid-type aberrations (telomere losses
and doublets) affecting the lagging strand telomeres, whereas DNA-PKcs-dependent NHEJ was responsible for sister telomere
fusions as a direct consequence of G-quadruplex formation and/or stabilization induced by 360A on parental telomere G strands.
NHEJ and HR activation at telomeres altered mitotic progression in treated cells. In particular, NHEJ-mediated sister telomere
fusions were associated with altered metaphase-anaphase transition and anaphase bridges and resulted in cell death during
mitosis or early G1. Collectively, these data elucidate specific molecular and cellular mechanisms triggered by telomere targeting
by the G-quadruplex ligand 360A, leading to cancer cell death. 相似文献
47.
Voltage-gated calcium channels are important mediators of calcium influx into electrically excitable cells. The amount of
calcium entering through this family of channel proteins is not only determined by the functional properties of channels embedded
in the plasma membrane but also by the numbers of channels that are expressed at the cell surface. The trafficking of channels
is controlled by numerous processes, including co-assembly with ancillary calcium channel subunits, ubiquitin ligases, and
interactions with other membrane proteins such as G protein coupled receptors. Here we provide an overview about the current
state of knowledge of calcium channel trafficking to the cell membrane, and of the mechanisms regulating the stability and
internalization of this important ion channel family. 相似文献
48.
Although all nucleated cells within a multicellular organism contain a complete copy of the genome, cell identity relies on
the expression of a specific subset of genes. Therefore, when cells divide they must not only copy their genome to their daughters,
but also ensure that the pattern of gene expression present before division is restored. While the carrier of this epigenetic
memory has been a topic of much research and debate, post-translational modifications of histone proteins have emerged in
the vanguard of candidates. In this paper we examine the mechanisms by which histone post-translational modifications are
propagated through DNA replication and cell division, and we critically examine the evidence that they can also act as vectors
of epigenetic memory. Finally, we consider ways in which epigenetic memory might be disrupted by interfering with the mechanisms
of DNA replication. 相似文献
49.
Valiokas R 《Cellular and molecular life sciences : CMLS》2012,69(3):347-356
The actual progress towards biological chip devices consisting of nanostructured functional entities is summarized. The practical
aspects of molecular nanobiochips are discussed, including the main surface chemistry platforms, as well as conventional and
unconventional fabrication tools. Several successful biological demonstrations of the first generation of nanobiochip devices
(mainly, different nanoarrays) are highlighted with the aim of revealing the potential of this technology in life sciences,
medicine, and related areas. 相似文献
50.
Toll-like receptors (TLRs) are a class of pattern recognition receptors sensing microbial components and triggering an immune
response against pathogens. In addition to their role in anti-infection immunity, increasing evidence indicates that engagement
of TLRs can promote cancer cell survival and proliferation, induce tumor immune evasion, and enhance tumor metastasis and
chemoresistance. Recent studies have demonstrated that endogenous molecules or damage-associated molecular patterns released
from damaged/necrotic tissues are capable of activating TLRs and that the endogenous ligands-mediated TLR signaling is implicated
in the tumor development and affects the therapeutic efficacy of tumors. Since both exogenous and endogenous TLR ligands can
initiate TLR signaling, which is the most valuable player in tumor development becomes an interesting question. Here, we summarize
the effect of TLR signaling on the development and progression of tumors, and discuss the role of exogenous and endogenous
TLR ligands in the tumorigenesis. 相似文献