Hutchison Michele R, Bassett Mary H, White Perrin C
Division of Pediatric Endocrinology, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9063, USA.
Mol Endocrinol. 2010 Jan;24(1):193-203. doi: 10.1210/me.2009-0228. Epub 2009 Nov 6.
We previously demonstrated that bovine epiphyseal chondrocytes separated by density gradient centrifugation differ in proliferative response to IGF-I and IGF-I receptor number. To identify novel modifiers of IGF-I action at the growth plate, we used microarray analyses to compare bovine hypertrophic and reserve zones and identified several receptors differentially expressed across the growth plate: NTRK2 [receptor for brain-derived neurotrophic factor (BDNF)], KIT [receptor for stem cell factor (SCF)], and MER and AXL [two receptors for growth arrest-specific 6 (Gas6)]. The corresponding ligands were tested for their ability to stimulate either proliferation of isolated chondrocytes or differentiation in ATDC5 cells. Each factor inhibited IGF-I-mediated proliferation in isolated chondrocytes by attenuating ERK1/2 activation. SCF, BDNF, Gas6, and C-type natriuretic peptide promoted differentiation in ATDC5 cells, each factor producing different expression patterns for collagen X, collagen 2, aggrecan, and lysyl oxidase. Whereas multiple factors stimulated ATDC5 differentiation, only IGF-I and high-dose insulin, out of several factors implicated in chondrocyte maturation, stimulated proliferation of isolated chondrocytes. IGF-I appears to be the primary proliferative signal in growth plate chondrocytes, whereas multiple factors including SCF, BDNF, and Gas6 regulate the pace of differentiation at the growth plate.
我们之前证明,通过密度梯度离心分离的牛骨骺软骨细胞对胰岛素样生长因子-I(IGF-I)的增殖反应以及IGF-I受体数量存在差异。为了确定生长板处IGF-I作用的新型调节因子,我们使用微阵列分析比较了牛的肥大区和储备区,并鉴定出几种在整个生长板中差异表达的受体:神经营养酪氨酸激酶2(NTRK2)[脑源性神经营养因子(BDNF)的受体]、干细胞因子受体(KIT)[干细胞因子(SCF)的受体],以及MER和AXL[生长停滞特异性蛋白6(Gas6)的两种受体]。测试了相应配体刺激分离软骨细胞增殖或ATDC5细胞分化的能力。每种因子通过减弱细胞外信号调节激酶1/2(ERK1/2)的激活来抑制IGF-I介导的分离软骨细胞增殖。SCF、BDNF、Gas6和C型利钠肽促进ATDC5细胞分化,每种因子产生不同的X型胶原、Ⅱ型胶原、聚集蛋白聚糖和赖氨酰氧化酶表达模式。虽然多种因子刺激ATDC5细胞分化,但在与软骨细胞成熟相关的几种因子中,只有IGF-I和高剂量胰岛素刺激分离软骨细胞增殖。IGF-I似乎是生长板软骨细胞中的主要增殖信号,而包括SCF、BDNF和Gas6在内的多种因子调节生长板处的分化速度。