Dept. Biochemistry and Molecular Biology, University of Maryland, School of Medicine, Baltimore, MD 21201, USA.
Mech Dev. 2011 Mar-Apr;128(3-4):234-45. doi: 10.1016/j.mod.2010.11.007. Epub 2010 Dec 1.
The expression pattern for tissue transglutaminase (TG2) suggests that it regulates cartilage formation. We analyzed the role of TG2 in early stages of chondrogenesis using differentiating high-density cultures of mesenchymal cells from chicken limb bud as a model. We demonstrate that TG2 promotes cell differentiation towards a pre-hypertrophic stage without inducing precocious hypertrophic maturation. This finding, combined with distinctive up-regulation of extracellular TG2 in the pre-hypertrophic cartilage of the growth plate, indicates that TG2 is an autocrine regulator of chondrocyte differentiation. We also show that TG2 regulates synthesis of the cartilaginous glycosaminoglycan (GAG)-rich extracellular matrix. Elevated levels of TG2 down-regulate xylosyltransferase activity which mediates the key steps in chondroitin sulfate synthesis. On the contrary, inhibition of endogenous transglutaminase activity in differentiating chondrogenic micromasses results in increased GAG deposition and enhancement of early chondrogenic markers. Regulation of GAG synthesis by TG2 appears independent of TGF-β activity, which is a downstream mediator of the TG2 functions in some biological systems. Instead, our data suggest a major role for cAMP/PKA signaling in transmitting TG2 signals in early chondrogenic differentiation. In summary, we demonstrate that matrix synthesis and early stages of chondrogenic differentiation are regulated through a novel mechanism involving TG2-dependent inhibition of PKA. These findings further advance understanding of cartilage formation and disease, and contribute to cartilage bioengineering.
组织转谷氨酰胺酶 (TG2) 的表达模式表明它可以调节软骨形成。我们使用鸡肢芽间充质细胞的高密度分化培养作为模型,分析了 TG2 在软骨发生早期阶段的作用。我们证明,TG2 促进细胞向预肥大阶段分化,而不会诱导过早的肥大成熟。这一发现,加上生长板预肥大软骨中外源 TG2 的独特上调,表明 TG2 是软骨细胞分化的自分泌调节剂。我们还表明,TG2 调节软骨糖胺聚糖 (GAG) 丰富的细胞外基质的合成。高水平的 TG2 下调介导软骨素硫酸盐合成关键步骤的木糖基转移酶活性。相反,在分化的软骨形成微团中抑制内源性转谷氨酰胺酶活性会导致 GAG 沉积增加和早期软骨形成标志物增强。TG2 对 GAG 合成的调节似乎独立于 TGF-β 活性,后者是 TG2 在某些生物系统中的功能的下游介质。相反,我们的数据表明 cAMP/PKA 信号转导在早期软骨发生分化中传递 TG2 信号具有重要作用。总之,我们证明了通过涉及 TG2 依赖性抑制 PKA 的新机制来调节基质合成和早期软骨分化。这些发现进一步推进了对软骨形成和疾病的理解,并为软骨生物工程做出了贡献。