Gushwa Nathan N, Hayashi Derek, Kemper Andrea, Abram Beverly, Taylor Jane E, Upton Jason, Tay Chloe F, Fiedler Sarah, Pullen Sam, Miller Linnsey P, Tallman Gary
Department of Biology, Willamette University, 900 State Street, Salem, Oregon 97301, USA.
Plant Physiol. 2003 Aug;132(4):1925-40. doi: 10.1104/pp.103.024067.
When guard cell protoplasts (GCPs) of tree tobacco [Nicotiana glauca (Graham)] are cultured at 32 degrees C with an auxin (1-napthaleneacetic acid) and a cytokinin (6-benzylaminopurine), they reenter the cell cycle, dedifferentiate, and divide. GCPs cultured similarly but at 38 degrees C and with 0.1 micro M +/- -cis,trans-abscisic acid (ABA) remain differentiated. GCPs cultured at 38 degrees C without ABA dedifferentiate partially but do not divide. Cell survival after 1 week is 70% to 80% under all of these conditions. In this study, we show that GCPs cultured for 12 to 24 h at 38 degrees C accumulate heat shock protein 70 and develop a thermotolerance that, upon transfer of cells to 32 degrees C, enhances cell survival but inhibits cell cycle reentry, dedifferentiation, and division. GCPs dedifferentiating at 32 degrees C require both 1-napthaleneacetic acid and 6-benzylaminopurine to survive, but thermotolerant GCPs cultured at 38 degrees C +/- ABA do not require either hormone for survival. Pulse-labeling experiments using 5-bromo-2-deoxyuridine indicate that culture at 38 degrees C +/- ABA prevents dedifferentiation of GCPs by blocking cell cycle reentry at G1/S. Cell cycle reentry at 32 degrees C is accompanied by loss of a 41-kD polypeptide that cross-reacts with antibodies to rat (Rattus norvegicus) extracellular signal-regulated kinase 1; thermotolerant GCPs retain this polypeptide. A number of polypeptides unique to thermotolerant cells have been uncovered by Boolean analysis of two-dimensional gels and are targets for further analysis. GCPs of tree tobacco can be isolated in sufficient numbers and with the purity required to study plant cell thermotolerance and its relationship to plant cell survival, growth, dedifferentiation, and division in vitro.
当树烟草[黄花烟草(格雷厄姆)]的保卫细胞原生质体(GCPs)在32℃下与生长素(1-萘乙酸)和细胞分裂素(6-苄基腺嘌呤)一起培养时,它们重新进入细胞周期,去分化并分裂。以类似方式培养但在38℃且添加0.1μM±顺,反式脱落酸(ABA)的GCPs保持分化状态。在38℃无ABA条件下培养的GCPs部分去分化但不分裂。在所有这些条件下,1周后的细胞存活率为70%至80%。在本研究中,我们表明在38℃下培养12至24小时的GCPs积累热休克蛋白70并产生耐热性,当将细胞转移至32℃时,这种耐热性可提高细胞存活率,但会抑制细胞周期重新进入、去分化和分裂。在32℃下去分化的GCPs需要1-萘乙酸和6-苄基腺嘌呤两者才能存活,但在38℃±ABA条件下培养的耐热GCPs存活不需要任何一种激素。使用5-溴-2-脱氧尿苷的脉冲标记实验表明,在38℃±ABA条件下培养可通过在G1/S期阻断细胞周期重新进入来防止GCPs去分化。在32℃时细胞周期重新进入伴随着一种41-kD多肽的丢失,该多肽与大鼠(褐家鼠)细胞外信号调节激酶1的抗体发生交叉反应;耐热GCPs保留了这种多肽。通过二维凝胶的布尔分析发现了一些耐热细胞特有的多肽,它们是进一步分析的目标。树烟草的GCPs可以大量分离且纯度足以用于研究植物细胞耐热性及其与植物细胞在体外存活、生长、去分化和分裂的关系。