The epidermal-growth-control theory of stem elongation : An old and a new perspective

The botanist G. Kraus postulated in 1867 that the peripheral cell layers determine the rate of organ elongation based on the observation that the separated outer and inner tissues of growing stems spontaneously change their lengths upon isolation from each other. Here, we summarize the modern version of this classical concept, the ‘‘epidermal-growth-control’’ or ‘‘tensile skin’’ theory of stem elongation. First, we present newly acquired data from sunflower hypocotyls, which demonstrate that the expansion of the isolated inner tissues is not an experimental artefact, as recently claimed, but rather the result of metabolism-independent cell elongation caused by the removal of the growth-controlling peripheral walls. Second, we present data showing that auxin-induced elongation of excised stem segments is attributable to the loosening of the thick epidermal walls, which provides additional evidence for the ‘‘epidermal-growth-control concept’’. Third, we show that the cuticle of aerial organs can be thin and mechanically weak in seedlings raised at high humidity, but thick and mechanically important for organs growing under relatively dry air conditions. Finally, we present a modified model of the ‘‘tensile skin-theory’’ that draws attention to the mechanical and physiological roles of (a) the thickened, helicoidal outer cell walls, (b) the mechanical constraint of a cuticle, and (c) the interactions among outer and inner cell layers as growth is coordinated by hormonal signals. & 2007 Elsevier GmbH. All rights reserved.

[1]  Cathie Martin,et al.  Functional aspects of cell patterning in aerial epidermis. , 2007, Current opinion in plant biology.

[2]  L. Schreiber,et al.  Protecting against water loss: analysis of the barrier properties of plant cuticles. , 2001, Journal of experimental botany.

[3]  P. Schopfer,et al.  Biomechanics of plant growth. , 2006, American journal of botany.

[4]  U. Kutschera,et al.  Auxin Enhancement of mRNAs in Epidermis and Internal Tissues of the Pea Stem and Its Significance for Control of Elongation. , 1990, Plant physiology.

[5]  J. Boyer Cell enlargement and growth-induced water potentials , 1988 .

[6]  W. Peters,et al.  What makes plants different? Principles of extracellular matrix function in 'soft' plant tissues. , 2000, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.

[7]  K Niklas,et al.  The role of the epidermis as a stiffening agent in Tulipa (Liliaceae) stems. , 1997, American journal of botany.

[8]  S. Fry Primary cell wall metabolism: tracking the careers of wall polymers in living plant cells. , 2004, The New phytologist.

[9]  D. Cosgrove Growth of the plant cell wall , 2005, Nature Reviews Molecular Cell Biology.

[10]  L. Jost Vorlesungen über Pflanzenphysiologie , 1908 .

[11]  U. Kutschera The current status of the acid‐growth hypothesis , 1994 .

[12]  C. Neinhuis,et al.  Biomechanics of isolated plant cuticles , 1998 .

[13]  U. Kutschera Stem Elongation and Cell Wall Proteins in Flowering Plants , 2001 .

[14]  Ulrich Kutschera,et al.  Tissue stresses in growing plant organs , 1989 .

[15]  J. Boyer,et al.  Direct Demonstration of a Growth-Induced Water Potential Gradient , 1993, Plant physiology.

[16]  Karl J. Niklas,et al.  Endosymbiosis, cell evolution, and speciation , 2005, Theory in Biosciences.

[17]  Karl J. Niklas,et al.  The Evolution of Plant Body Plans—A Biomechanical Perspective , 2000 .

[18]  U. Kutschera,et al.  Differential effect of auxin on in vivo extensibility of cortical cylinder and epidermis in pea internodes. , 1987, Plant physiology.

[19]  J. Verbelen,et al.  Cellulose orientation determines mechanical anisotropy in onion epidermis cell walls. , 2006, Journal of experimental botany.

[20]  H. Edelmann Lateral redistribution of auxin is not the means for gravitropic differential growth of coleoptiles: A new model. , 2001, Physiologia plantarum.

[21]  John S. Boyer,et al.  Tissue stresses and resistance to water flow conspire to uncouple the water potential of the epidermis from that of the xylem in elongating plant stems. , 2003, Functional plant biology : FPB.

[22]  U. Kutschera,et al.  Growth, in vivo extensibility, and tissue tension in developing pea internodes. , 1988, Plant physiology.

[23]  F. Baluška,et al.  Eukaryotic cells and their cell bodies: Cell Theory revised. , 2004, Annals of botany.

[24]  U. Kutschera,et al.  Interaction between cortical cylinder and epidermis during auxin-mediated growth in pea internodes , 1988 .

[25]  A. Heyn The physiology of cell elongation , 1940, The Botanical Review.

[26]  K. Niklas The evolutionary biology of plants , 1997 .

[27]  K. Niklas,et al.  Preferential states of longitudinal tension in the outer tissues of Taraxcum officinale (Asteraceae) peduncles. , 1998, American journal of botany.

[28]  Zygmunt Hejnowicz,et al.  Graviresponses in herbs and trees: a major role for the redistribution of tissue and growth stresses , 1997, Planta.

[29]  P. Schopfer Determination of Auxin-Dependent pH Changes in Coleoptile Cell Walls by a Null-Point Method , 1993, Plant physiology.

[30]  U. Kutschera,et al.  Tissue pressure and cell-wall metabolism in auxin-mediated growth of sunflower hypocotyls , 1993 .

[31]  J. A. Bartsch,et al.  Biomechanics and anatomy of Lycopersicon esculentum fruit peels and enzyme-treated samples. , 2004, American journal of botany.

[32]  William J Lucas,et al.  Plasmodesmata and the supracellular nature of plants. , 1993, The New phytologist.

[33]  A. D. Tomos,et al.  The Epidermis Still in Control , 1996 .

[34]  T. Munnik,et al.  Life under pressure: hydrostatic pressure in cell growth and function. , 2007, Trends in plant science.

[35]  P. Schopfer,et al.  Cooperation of epidermis and inner tissues in auxin-mediated growth of maize coleoptiles , 1987, Planta.

[36]  H. Edelmann Wall extensibility during hypocotyl growth: A hypothesis to explain elastic-induced wall loosening , 1995 .

[37]  D J Cosgrove,et al.  Enzymes and other agents that enhance cell wall extensibility. , 1999, Annual review of plant physiology and plant molecular biology.

[38]  U. Kutschera Acid Growth and Plant Development , 2006, Science.

[39]  A. D. Tomos,et al.  The history of tissue tension. , 1996, Annals of botany.

[40]  Y. Masuda Auxin-induced cell elongation and cell wall changes , 1990, The botanical magazine = Shokubutsu-gaku-zasshi.

[41]  P. Schopfer,et al.  Plasma membrane‐generated reactive oxygen intermediates and their role in cell growth of plants , 2006, BioFactors.

[42]  J. Boyer,et al.  Hydraulics of plant growth. , 2004, Functional plant biology : FPB.

[43]  W F Decraemer,et al.  Cell walls at the plant surface behave mechanically like fiber-reinforced composite materials. , 2001, Plant physiology.

[44]  Stephen C. Fry,et al.  The Growing Plant Cell Wall: Chemical and Metabolic Analysis , 2001 .

[45]  Karl J. Niklas,et al.  MECHANICAL BEHAVIOR OF PLANT TISSUES AS INFERRED FROM THE THEORY OF PRESSURIZED CELLULAR SOLIDS , 1989 .

[46]  R. Cleland Cell Wall Extension , 1971 .

[47]  R. Firn,et al.  The Role of the Peripheral Cell Layers in the Geotropic Curvature of Sunflower Hypocotyls: a New Model of Shoot Geotropism , 1977 .

[48]  K. Niklas,et al.  Springer-Verlag 2004 , 2004 .

[49]  Markus Riederer,et al.  Estimating Partitioning and Transport of Organic Chemicals in the Foliage/Atmosphere System: Discussion of a Fugacity-Based Model , 1990 .

[50]  L. Taiz,et al.  Plant Cell Expansion: Regulation of Cell Wall Mechanical Properties , 1984 .

[51]  Joanne Chory,et al.  The epidermis both drives and restricts plant shoot growth , 2007, Nature.

[52]  U. Kutschera,et al.  Gravitropism of axial organs in multicellular plants. , 2001, Advances in space research : the official journal of the Committee on Space Research.

[53]  U. Kutschera Cell expansion in plant development. , 2000 .

[54]  U. Kutschera The Role of the Epidermis in the Control of Elongation Growth in Stems and Coleoptiles , 1992 .

[55]  K. Esau Anatomy of seed plants , 1960 .

[56]  Chris Somerville,et al.  Cellulose synthesis in higher plants. , 2006, Annual review of cell and developmental biology.

[57]  L. Pienaar,et al.  The predominant role of the pith in the Growth and development of internodes in Liquidambar styraciflua (Hamamelidaceae). I. Histological basis of compressive and tensile stresses in developing primary tissues , 1995 .

[58]  D. Paolillo,et al.  Crack Resistance in Cherry Tomato Fruit Correlates with Cuticular Membrane Thickness , 2004 .

[59]  D. R. Kaplan The Relationship of Cells to Organisms in Plants: Problem and Implications of an Organismal Perspective , 1992, International Journal of Plant Sciences.

[60]  A. D. Tomos,et al.  The mechanic state of "inner tissue" in the growing zone of sunflower hypocotyls and the regulation of its growth rate following excision. , 2000, Plant physiology.

[61]  M. J. Bukovac,et al.  Rheological Properties of Enzymatically Isolated Tomato Fruit Cuticle , 1995, Plant physiology.

[62]  J. Boyer,et al.  Identifying cytoplasmic input to the cell wall of growing Chara corallina. , 2006, Journal of experimental botany.

[63]  U. Kutschera Cell-wall synthesis and elongation growth in hypocotyls of Helianthus annuus L. , 1990, Planta.