Department of Neurobiology, Harvard Medical School and Howard Hughes Medical Institute, Boston, Massachusetts 02115, USA.
Nature. 2012 Jan 15;481(7382):520-4. doi: 10.1038/nature10745.
Hair cells of the inner ear are not normally replaced during an animal's life, and must continually renew components of their various organelles. Among these are the stereocilia, each with a core of several hundred actin filaments that arise from their apical surfaces and that bear the mechanotransduction apparatus at their tips. Actin turnover in stereocilia has previously been studied by transfecting neonatal rat hair cells in culture with a β-actin-GFP fusion, and evidence was found that actin is replaced, from the top down, in 2-3 days. Overexpression of the actin-binding protein espin causes elongation of stereocilia within 12-24 hours, also suggesting rapid regulation of stereocilia lengths. Similarly, the mechanosensory 'tip links' are replaced in 5-10 hours after cleavage in chicken and mammalian hair cells. In contrast, turnover in chick stereocilia in vivo is much slower. It might be that only certain components of stereocilia turn over quickly, that rapid turnover occurs only in neonatal animals, only in culture, or only in response to a challenge like breakage or actin overexpression. Here we quantify protein turnover by feeding animals with a (15)N-labelled precursor amino acid and using multi-isotope imaging mass spectrometry to measure appearance of new protein. Surprisingly, in adult frogs and mice and in neonatal mice, in vivo and in vitro, the stereocilia were remarkably stable, incorporating newly synthesized protein at <10% per day. Only stereocilia tips had rapid turnover and no treadmilling was observed. Other methods confirmed this: in hair cells expressing β-actin-GFP we bleached fiducial lines across hair bundles, but they did not move in 6 days. When we stopped expression of β- or γ-actin with tamoxifen-inducible recombination, neither actin isoform left the stereocilia, except at the tips. Thus, rapid turnover in stereocilia occurs only at the tips and not by a treadmilling process.
内耳的毛细胞在动物的一生中通常不会被替换,必须不断更新它们各种细胞器的成分。其中包括静纤毛,每根静纤毛的顶端表面都有数百根肌动蛋白丝的核心,这些丝的顶端承载着机械转导装置。以前通过在培养的新生大鼠毛细胞中转染β-肌动蛋白-GFP 融合蛋白来研究静纤毛中的肌动蛋白周转,发现肌动蛋白从顶部到底部在 2-3 天内被替换。肌动蛋白结合蛋白 espin 的过表达会在 12-24 小时内导致静纤毛伸长,这也表明静纤毛长度的快速调节。同样,鸡和哺乳动物毛细胞中的机械感觉“尖端连接”在切割后 5-10 小时内被替换。相比之下,体内雏鸡静纤毛的周转速度要慢得多。可能只有静纤毛的某些成分快速周转,快速周转仅发生在新生动物、培养物中,或仅在受到挑战(如断裂或肌动蛋白过表达)时才发生。在这里,我们通过用(15)N 标记的前体氨基酸喂养动物,并使用多同位素成像质谱测量新蛋白的出现来定量蛋白质周转。令人惊讶的是,在成年青蛙和老鼠以及新生老鼠中,无论是体内还是体外,静纤毛都非常稳定,每天仅掺入新合成的蛋白质<10%。只有静纤毛的尖端有快速周转,没有发现链轨运动。其他方法证实了这一点:在表达β-肌动蛋白-GFP 的毛细胞中,我们用荧光漂白法横跨毛束标记基准线,但在 6 天内它们没有移动。当我们用他莫昔芬诱导的重组停止β-或γ-肌动蛋白的表达时,两种肌动蛋白同工型都没有离开静纤毛,除了尖端。因此,静纤毛的快速周转仅发生在尖端,而不是通过链轨运动过程。