Laboratory of Cell Physiology, Growth and Development, Cornell University, 252 Clark Hall, 14850, Ithaca, New York, USA.
Planta. 1973 Sep;111(3):219-43. doi: 10.1007/BF00385106.
Earlier papers of this series relate to different growth-promoting substances and systems which, singly and in combination, have interacted with trace elements (Mn and Mo) and Fe to induce growth and to affect the metabolism of aseptic cultures of carrot. The solutes of cultured carrot cells (K(+), Na(+), Cl(-), total solutes) are also affected. Two clones were grown in 9 combinations of growth factors and under 4 trace-element regimes (a complete complement including Fe, and this complement lacking either Mn or Mo, or both Mn and Mo), a total of 36 treatments under otherwise standardized experimental conditions. Under the treatments applied the number of cells varied over a 35fold range and their average size over a 7fold range; the concomitant effects on their solutes are expressed in terms of concentrations and of total content per cell. Both growth and the solutes accumulated were variously affected by carrot growth-promoting system I (mediated by inositol), by system II (mediated by IAA), and by coconut milk in the presence of Fe, with and without Mn, Mo, or Mn and Mo.The greatest concentrations of total solutes occurred in tissue cultured in nutrient solutions which lacked the stimuli to rapid cell multiplication and were also limited by the trace elements Mn and Mo. Moreover, specific regulatory effects of the trace elements on solute content, not solely attributable to their effects on cell growth, have been noted. An imbalanced growth-factor regime (zeatin acting alone, i.e. without IAA) shifted the normal preference for K(+) over Na(+) strongly toward Na(+), a trend which could also be induced by certain trace elements and more balanced growth-factor regimes, e.g. in a basal coconut milk medium lacking only Mn.The data are interpreted in the context of views on the de-novo uptake of salts and solutes in cultured cells as they grow. These cells respond to a network, or matrix, of interacting factors by distinctive effects that are attributable to the component parts of the culture medium acting singly and in various combinations. These interactions (involving trace elements and exogenous growth factors) control growth (fresh weight, number and size of cells) and regulate the solutes (organic and inorganic; K(+) vs. Na(+); organic anions vs. Cl(-)) which the cells acquire as they grow and develop. The intensity of the response of the cultures to balanced, or imbalanced, growth factors creates the internal spaces accessible to solutes; and the metabolism, as it is also affected by growth factors and trace elements, determines how these spaces are to be filled at a given osmotic value. The evidence shows the range of factors that affect the accumulation of solutes in cells as they grow and is to be contrasted with conventional observations on mature cells held in steady states under conditions that preclude all growth and when only a single ionic species is followed over a very short interval of time.
早期的论文涉及不同的生长促进物质和系统,它们单独或组合作用于痕量元素(Mn 和 Mo)和 Fe 以诱导生长并影响胡萝卜无菌培养物的代谢。培养的胡萝卜细胞的溶质(K(+)、Na(+)、Cl(-)、总溶质)也受到影响。在 4 种痕量元素(完整补充物包括 Fe,以及缺乏 Mn 或 Mo 或两者的补充物)和 36 种处理下,两种克隆在 9 种生长因子组合下生长,在其他标准化实验条件下。在应用的处理下,细胞数量变化范围为 35 倍,细胞平均大小变化范围为 7 倍;对其溶质的伴随影响以浓度和每个细胞的总含量表示。胡萝卜生长促进系统 I(由肌醇介导)、系统 II(由 IAA 介导)和椰子乳在 Fe 存在下、有或没有 Mn、Mo 或 Mn 和 Mo 时,以及生长和积累的溶质都受到不同程度的影响。在缺乏快速细胞增殖刺激物且受到 Mn 和 Mo 痕量元素限制的营养溶液中培养的组织中,总溶质的浓度最大。此外,还注意到痕量元素对溶质含量的特定调节作用,而不仅仅归因于它们对细胞生长的影响。不平衡的生长因子(仅由玉米素作用,即没有 IAA)强烈地将对 K(+)的正常偏好转移到 Na(+)上,这种趋势也可以被某些痕量元素和更平衡的生长因子诱导,例如在仅缺乏 Mn 的基础椰子乳培养基中。这些数据是在关于培养细胞在生长过程中盐和溶质从头吸收的观点的背景下解释的。这些细胞通过独特的影响对相互作用的因素网络或基质做出反应,这些影响归因于培养基的组成部分单独和各种组合的作用。这些相互作用(涉及痕量元素和外源性生长因子)控制生长(鲜重、细胞数量和大小)并调节细胞获取的溶质(有机和无机;K(+)与 Na(+);有机阴离子与 Cl(-)),随着细胞的生长和发育,这些溶质被调节。培养物对平衡或不平衡生长因子的反应强度为溶质提供了可进入的内部空间;而代谢,也受到生长因子和痕量元素的影响,决定了在给定渗透压下如何填充这些空间。证据表明了影响细胞在生长过程中溶质积累的因素范围,并与在排除所有生长且仅在很短时间内跟踪单个离子物种的情况下处于稳定状态的成熟细胞的常规观察结果形成对比。