Lauing Kristen L, Cortes Mauricio, Domowicz Miriam S, Henry Judith G, Baria Alexis T, Schwartz Nancy B
Department of Pediatrics, The University of Chicago, Chicago IL 60637, USA.
Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637, USA.
Dev Biol. 2014 Dec 15;396(2):224-36. doi: 10.1016/j.ydbio.2014.10.005. Epub 2014 Oct 18.
The proteoglycan aggrecan is a prominent component of the extracellular matrix in growth plate cartilage. A naturally occurring, recessive, perinatally lethal mutation in the aggrecan core protein gene, cmd(bc) (Acan(cmd-Bc)), that deletes the entire protein-coding sequence provided a model in which to characterize the phenotypic and morphologic effects of aggrecan deletion on skeletal development. We also generated a novel transgenic mouse, Tg(COL2A1-ACAN), that has the chick ACAN coding sequence driven by the mouse COL2A1 promoter to enable the production of cmd(bc)/cmd(bc); Tg(COL2A1-ACAN) rescue embryos. These were used to assess the impact of aggrecan on growth plate organization, chondrocyte survival and proliferation, and the expression of mRNAs encoding chondrocyte differentiation markers and growth factors. Homozygous mutant (cmd(bc)/cmd(bc)) embryos exhibited severe defects in all skeletal elements with deformed and shortened (50%) limb elements. Expression of aggrecan in rescue embryos reversed the skeletal defects to varying degrees with a 20% increase in limb element length and near-full reversal (80%) of size and diameter of the ribcage and vertebrae. Aggrecan-null growth plates were devoid of matrix and lacked chondrocyte organization and differentiation, while those of the rescue embryos exhibited matrix production concomitant with partial zonation of chondrocytes having proliferative and hypertrophic morphologies. Deformation of the trachea, likely the cause of the mutation's lethality, was reduced in the rescue embryos. Aggrecan-null embryos also had abnormal patterns of COL10A1, SOX9, IHH, PTCH1, and FGFR3 mRNA expression in the growth plate. Expression of chick aggrecan in the rescue embryos notably increased COLX expression, accompanied by the reappearance of a hypertrophic zone and IHH expression. Significantly, in transgenic rescue embryos, the cell death and decreased proliferation phenotypes exhibited by the mutants were reversed; both were restored to wild-type levels. These findings suggest that aggrecan has a major role in regulating the expression of key growth factors and signaling molecules during development of cartilaginous tissue and is essential for proper chondrocyte organization, morphology, and survival during embryonic limb development.
蛋白聚糖聚集蛋白聚糖是生长板软骨细胞外基质的重要组成部分。聚集蛋白聚糖核心蛋白基因中一种自然发生的隐性围产期致死突变cmd(bc)(Acan(cmd-Bc)),该突变删除了整个蛋白质编码序列,提供了一个模型,用于表征聚集蛋白聚糖缺失对骨骼发育的表型和形态学影响。我们还构建了一种新型转基因小鼠Tg(COL2A1-ACAN),其具有由小鼠COL2A1启动子驱动的鸡ACAN编码序列,以产生cmd(bc)/cmd(bc); Tg(COL2A1-ACAN)拯救胚胎。这些胚胎用于评估聚集蛋白聚糖对生长板组织、软骨细胞存活和增殖以及编码软骨细胞分化标志物和生长因子的mRNA表达的影响。纯合突变体(cmd(bc)/cmd(bc))胚胎在所有骨骼元素中均表现出严重缺陷,肢体元素变形且缩短(50%)。拯救胚胎中聚集蛋白聚糖的表达不同程度地逆转了骨骼缺陷,肢体元素长度增加了20%,胸腔和椎骨的大小和直径几乎完全逆转(80%)。缺乏聚集蛋白聚糖的生长板没有基质,缺乏软骨细胞组织和分化,而拯救胚胎的生长板表现出基质产生,同时伴有具有增殖和肥大形态的软骨细胞部分分区。气管变形可能是突变致死的原因,在拯救胚胎中有所减轻。缺乏聚集蛋白聚糖的胚胎在生长板中COL10A1、SOX9、IHH、PTCH1和FGFR3 mRNA的表达模式也异常。拯救胚胎中鸡聚集蛋白聚糖的表达显著增加了COLX的表达,同时肥大带和IHH表达重新出现。重要的是,在转基因拯救胚胎中,突变体表现出的细胞死亡和增殖减少表型得到了逆转;两者均恢复到野生型水平。这些发现表明,聚集蛋白聚糖在软骨组织发育过程中对关键生长因子和信号分子的表达具有重要调节作用,并且对于胚胎肢体发育过程中软骨细胞的正常组织、形态和存活至关重要。