Tong A, Reich A, Genin O, Pines M, Monsonego-Ornan E
Institute of Animal Science, The Volcani Center, Bet Dagan, Israel.
J Bone Miner Res. 2003 Aug;18(8):1443-52. doi: 10.1359/jbmr.2003.18.8.1443.
A newly cloned avian 75-kDa gelatinase B-like enzyme is expressed by the cells surrounding the blood vessels of the growth plate and upregulated by angiogenic substances in cultured chondrocytes. Despite its low homology to mammalian gelatinase-B, the avian 75-kDa seems to function similarly in the context of endochondral bone formation.
Gelatinase B/metalloproteinase (MMP)-9, a zinc-dependent protease of the MMP family, is a key regulator in the final step of endochondral ossification. Recently an avian 75-kDa gelatinase B-like enzyme that shows low sequence similarity to the mammalian enzyme (59% on the protein level) was cloned and characterized. However, its expression pattern in the chicken growth plate and its role in bone formation have not, so far, been examined.
Based on the published sequence, we cloned a 700-bp fragment from cDNA of the chicken growth plate and studied its expression pattern in primary chondrocytes. Because the basal expression level of gelatinase B was almost undetectable, we induced its expression by different culturing conditions, the most dramatic induction achieved by treatment with retinoic acid, which is known as an inducer of vascular invasion in the epiphyseal plates. The gelatinolitic activity, checked by zymography, detected bands corresponding to the gelatinase A and B as well as a new high-molecular weight band of approximately 200 kDa. We further studied the expression pattern of gelatinase B by in situ hybridization. The gelatinase B was expressed by the cells surrounding the blood vessels penetrating the growth plate and by chondrocytes located in the front of these vascular invasions in the borders between the bone and the cartilage, resembling the expression of mouse gelatinase B in the growth plate. The induction of rickets by a vitamin D-deficient diet reduced the expression levels of gelatinase B in the growth plate of 12-day-old chickens but did not affect the expression of gelatinase A mRNA.
The chicken growth plate has a distinctly different structure from the mammalian one: it is much wider, it contains more cells in each zone, and the blood vessels penetrate deeper into the hypertrophic zone. Nevertheless, the upregulation of the avian 75-kDa gelatinase B-like enzyme by vitamins A and D, coupled with its perivascular expression pattern in the growth plate, implies a similar role for the mammalian and avian genes in bone formation.
一种新克隆的禽类75 kDa明胶酶B样酶由生长板血管周围的细胞表达,并在培养的软骨细胞中被血管生成物质上调。尽管其与哺乳动物明胶酶B的同源性较低,但禽类75 kDa酶在软骨内骨形成过程中似乎具有相似的功能。
明胶酶B/金属蛋白酶(MMP)-9是MMP家族的一种锌依赖性蛋白酶,是软骨内骨化最后一步的关键调节因子。最近,一种与哺乳动物酶序列相似性较低(蛋白质水平为59%)的禽类75 kDa明胶酶B样酶被克隆并进行了表征。然而,其在鸡生长板中的表达模式及其在骨形成中的作用迄今尚未得到研究。
根据已发表的序列,我们从鸡生长板的cDNA中克隆了一个700 bp的片段,并研究了其在原代软骨细胞中的表达模式。由于明胶酶B的基础表达水平几乎检测不到,我们通过不同的培养条件诱导其表达,其中最显著的诱导是用视黄酸处理,视黄酸是已知的骺板血管侵入诱导剂。通过酶谱法检测明胶分解活性,检测到与明胶酶A和B相对应的条带以及一条约200 kDa的新的高分子量条带。我们通过原位杂交进一步研究了明胶酶B的表达模式。明胶酶B由穿透生长板的血管周围的细胞以及位于骨与软骨边界处这些血管侵入前方的软骨细胞表达,类似于小鼠明胶酶B在生长板中的表达。维生素D缺乏饮食诱导佝偻病可降低12日龄鸡生长板中明胶酶B的表达水平,但不影响明胶酶A mRNA的表达。
鸡生长板的结构与哺乳动物生长板明显不同:它更宽,每个区域含有更多细胞,血管更深地穿透到肥大区。然而,维生素A和D对禽类75 kDa明胶酶B样酶的上调作用,以及其在生长板中的血管周围表达模式,意味着哺乳动物和禽类基因在骨形成中具有相似的作用。