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脊索、脊索细胞和 CTGF/CCN-2:从发育到成熟的持续活动。

The Notochord, Notochordal cell and CTGF/CCN-2: ongoing activity from development through maturation.

机构信息

Division of Orthopaedic Surgery, University of Toronto, Toronto Western Hospital, 399 Bathurst St., McLaughlin Pavilion Rm 13-415, Toronto, ON, M5T 2S8, USA,

出版信息

J Cell Commun Signal. 2008 Dec;2(3-4):59-65. doi: 10.1007/s12079-008-0031-5. Epub 2008 Nov 12.

Abstract

The growth regulating factor CTGF/CCN-2 is an integral factor in growth and development, connective tissue maintenance, wound repair and cell cycle regulation. It has recently been reported that CTGF/CCN-2 is involved in very early development having been detected in early notochord formation in zebrafish using CTGF/CCN-2 promoter-driven green fluorescent protein (GFP) plasmids. In these studies fluorescence was detected early in the developing embryos, a finding of considerable significance in that CTGF/CCN-2 deficient mutant mice die early after birth due to severe cartilage and skeletal dysplasia and respiratory failure. Such findings confirm the importance of CTGF/CCN-2 in development and of the necessary and sufficient role of this molecule in formation of the skeleton, extracellular matrix and chondrogenesis. Of particular relevance to the relationship between the notochordal cell and CTGF/CCN-2 there is a remarkable sub-species of canine, the 'non-chondrodystrophic' canine that is protected from developing degenerative disc disease (DDD). These animals are unique in that they preserve the population of notochordal cells within their disc nucleus (NP) and these cells secrete CTGF/CCN-2. We have detected CTGF/CCN-2 within conditioned medium developed from the notochordal cells of these animals (NCCM) and used this conditioned medium to demonstrate robustly increased proteoglycan production. The addition of recombinant human CTGF/CCN-2 to totally serum-free media containing cultures of bovine NP cells replicated the robustly increased aggrecan gene expression found with NCCM alone strongly suggesting the importance of the effect of CTGF/CCN-2 in notochordal cell biology within the disc nucleus of non-chondrodystrophic canines. The chondrodystrophic canine, another sub-species on the other hand are almost totally devoid of notochordal cells and they develop DDD profoundly and early. These two sub-species of canine reflect a naturally occurring animal model that is an excellent example of differential notochordal cell survival and possible associated developmental differences in extracellular maintenance.

摘要

生长调节因子 CTGF/CCN-2 是生长和发育、结缔组织维持、伤口修复和细胞周期调节的重要因素。最近有报道称,CTGF/CCN-2 参与了早期发育过程,在斑马鱼的早期脊索形成中,使用 CTGF/CCN-2 启动子驱动的绿色荧光蛋白 (GFP) 质粒检测到了 CTGF/CCN-2。在这些研究中,在发育中的胚胎早期就检测到了荧光,这一发现意义重大,因为 CTGF/CCN-2 缺失突变小鼠在出生后因严重的软骨和骨骼发育不良以及呼吸衰竭而早期死亡。这些发现证实了 CTGF/CCN-2 在发育中的重要性,以及该分子在骨骼形成、细胞外基质和软骨发生中的必要和充分作用。与脊索细胞和 CTGF/CCN-2 之间的关系特别相关的是一种非常特殊的犬种,即“非软骨发育不良”犬,这种犬种可以免受退行性椎间盘疾病 (DDD) 的影响。这些动物的独特之处在于,它们在椎间盘核 (NP) 内保留了脊索细胞的种群,这些细胞分泌 CTGF/CCN-2。我们已经在这些动物的脊索细胞产生的条件培养基 (NCCM) 中检测到 CTGF/CCN-2,并使用这种条件培养基证明了糖胺聚糖的大量产生。将重组人 CTGF/CCN-2 添加到完全不含血清的培养基中,培养牛 NP 细胞,复制了仅使用 NCCM 时发现的强有力的聚集蛋白聚糖基因表达,强烈表明 CTGF/CCN-2 在非软骨发育不良犬的椎间盘核内的脊索细胞生物学中的重要作用。另一方面,软骨发育不良犬是另一个亚种,几乎完全没有脊索细胞,它们很早就出现了 DDD 。这两个犬亚种反映了一种自然发生的动物模型,是脊索细胞存活和可能相关的细胞外维持发育差异的一个极好例子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ae3/2648046/ab2efab26a69/12079_2008_31_Fig1_HTML.jpg

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