Sehm Tina, Sachse Christoph, Frenzel Corina, Echeverri Karen
DFG Center for Regenerative Therapies (CRTD), c/o MPI-CBG Pfotenhauerstrasse 108, Dresden 01307, Germany.
Dev Biol. 2009 Oct 15;334(2):468-80. doi: 10.1016/j.ydbio.2009.08.008. Epub 2009 Aug 13.
Salamanders have the remarkable ability to regenerate many body parts following catastrophic injuries, including a fully functional spinal cord following a tail amputation. The molecular basis for how this process is so exquisitely well-regulated, assuring a faithful replication of missing structures every time, remains poorly understood. Therefore a study of microRNA expression and function during regeneration in the axolotl, Ambystoma mexicanum, was undertaken. Using microarray-based profiling, it was found that 78 highly conserved microRNAs display significant changes in expression levels during the early stages of tail regeneration, as compared to mature tissue. The role of miR-196, which was highly upregulated in the early tail blastema and spinal cord, was then further analyzed. Inhibition of miR-196 expression in this context resulted in a defect in regeneration, yielding abnormally shortened tails with spinal cord defects in formation of the terminal vesicle. A more detailed characterization of this phenotype revealed downstream components of the miR-196 pathway to include key effectors/regulators of tissue patterning within the spinal cord, including BMP4 and Pax7. As such, our dataset establishes miR-196 as an essential regulator of tail regeneration, acting upstream of key BMP4 and Pax7-based patterning events within the spinal cord.
蝾螈具有非凡的能力,能够在遭受灾难性损伤后再生许多身体部位,包括在尾巴截肢后再生出功能完全正常的脊髓。然而,对于这一过程如何得到如此精确调控,从而确保每次都能准确复制缺失结构的分子基础,我们仍知之甚少。因此,我们对墨西哥钝口螈(Ambystoma mexicanum)再生过程中的微小RNA(miRNA)表达和功能进行了研究。通过基于微阵列的分析,我们发现与成熟组织相比,78种高度保守的miRNA在尾巴再生早期阶段的表达水平发生了显著变化。随后,我们进一步分析了在早期尾巴芽基和脊髓中高度上调的miR-196的作用。在这种情况下抑制miR-196的表达会导致再生缺陷,产生异常缩短的尾巴,并在终末囊泡形成过程中出现脊髓缺陷。对这一表型的更详细特征分析揭示了miR-196途径的下游成分,包括脊髓内组织模式形成的关键效应器/调节因子,如BMP4和Pax7。因此,我们的数据表明miR-196是尾巴再生的关键调节因子,在脊髓内基于BMP4和Pax7的关键模式形成事件上游发挥作用。