Unbiased estimation of chloroplast number in mesophyll cells: advantage of a genuine three-dimensional approach
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24336344
PubMed Central
PMC3904715
DOI
10.1093/jxb/ert407
PII: ert407
Knihovny.cz E-zdroje
- Klíčová slova
- Chloroplast counting, Norway spruce (Picea abies L. Karst.), confocal microscopy, coniferous needle structure, disector method, mesophyll, profile counting, stereology.,
- MeSH
- biologické modely MeSH
- chloroplasty metabolismus MeSH
- mezofylové buňky cytologie metabolismus MeSH
- smrk MeSH
- zobrazování trojrozměrné metody MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Chloroplast number per cell is a frequently examined quantitative anatomical parameter, often estimated by counting chloroplast profiles in two-dimensional (2D) sections of mesophyll cells. However, a mesophyll cell is a three-dimensional (3D) structure and this has to be taken into account when quantifying its internal structure. We compared 2D and 3D approaches to chloroplast counting from different points of view: (i) in practical measurements of mesophyll cells of Norway spruce needles, (ii) in a 3D model of a mesophyll cell with chloroplasts, and (iii) using a theoretical analysis. We applied, for the first time, the stereological method of an optical disector based on counting chloroplasts in stacks of spruce needle optical cross-sections acquired by confocal laser-scanning microscopy. This estimate was compared with counting chloroplast profiles in 2D sections from the same stacks of sections. Comparing practical measurements of mesophyll cells, calculations performed in a 3D model of a cell with chloroplasts as well as a theoretical analysis showed that the 2D approach yielded biased results, while the underestimation could be up to 10-fold. We proved that the frequently used method for counting chloroplasts in a mesophyll cell by counting their profiles in 2D sections did not give correct results. We concluded that the present disector method can be efficiently used for unbiased estimation of chloroplast number per mesophyll cell. This should be the method of choice, especially in coniferous needles and leaves with mesophyll cells with lignified cell walls where maceration methods are difficult or impossible to use.
Zobrazit více v PubMed
Adachi S, Nakae T, Uchida M, et al. 2013. The mesophyll anatomy enhancing CO2 diffusion is a key trait for improving rice photosynthesis. Journal of Experimental Botany 64, 1061–1072 PubMed
Albrechtová J, Kubínová L. 1991. Quantitative analysis of the structure of etiolated barley leaf using stereological methods. Journal of Experimental Botany 42, 1311–1314
Albrechtová J, Janáček J, Lhotáková Z, Radochová B, Kubínová L. 2007. Novel efficient methods for measuring mesophyll anatomical characteristics from fresh thick sections using stereology and confocal microscopy: application on acid rain-treated Norway spruce needles. Journal of Experimental Botany 58, 1451–1461 PubMed
Bockers M, Čapková V, Tichá I, Schafer C. 1997. Growth at high CO2 affects the chloroplast number but not the photosynthetic efficiency of photoautotrophic Marchantia polymorpha culture cells. Plant Cell Tissue and Organ Culture 48, 103–110
Boffey SA, Ellis JR, Sellden G, Leech RM. 1979. Chloroplast division and DNA synthesis in light-grown wheat leaves. Plant Physiology 64, 502–505 PubMed PMC
Chaly N, Possingham JV, Thomson WW. 1980. Chloroplast division in spinach leaves examined by scanning electron-microscopy and freeze-etching. Journal of Cell Science 46, 87–96 PubMed
Coate JE, Luciano AK, Seralathan V, Minchew KJ, Owens TG, Doyle JJ. 2012. Anatomical, biochemical, and photosynthetic responses to recent allopolyploidy in Glycine dolichocarpa (Fabaceae). American Journal of Botany 99, 55–67 PubMed
Dean C, Leech RM. 1982. Genome expression during normal leaf development.1. Cellular and chloroplast numbers and DNA, RNA, and protein-levels in tissues of different ages within a 7-day-old wheat leaf. Plant Physiology 69, 904–910 PubMed PMC
Dinkins R., Srinivasa Reddy MS, Leng M, Collins GB. 2001. Overexpression of the Arabidopsis thaliana MinD1 gene alters chloroplast size and number in transgenic tobacco plants. Planta 214, 180–188 PubMed
Ellis JR, Leech RM. 1985. Cell-size and chloroplast size in relation to chloroplast replication in light-grown wheat leaves. Planta 165, 120–125 PubMed
Frandsen N. 1968. Die Plastidenzahl als Merkmal bei der Kartoffel. Theoretical and Applied Genetics 38, 153–167 PubMed
Gopi R, Jaleel CA, Panneerselvam R. 2008. Leaf anatomical responses of Amorphophallus campanulatus to triazoles fungicides. EurAsian Journal of BioSciences 2, 46–52
Gundersen HJG. 1986. Stereology of arbitrary particles—a review of unbiased number and size estimators and the presentation of some new ones, in memory of Thompson, William, R. Journal of Microscopy 143, 3–45 PubMed
Gundersen HJG, Jensen EB. 1987. The efficiency of systematic sampling in stereology and its prediction. Journal of Microscopy 147, 229–263 PubMed
Gundersen HJG. 1977. Notes on the estimation of the numerical density of arbitrary profiles: the edge effect. Journal of Microscopy 111, 219–223
Hassan L, Wazuddin M. 2000. Colchicine-induced variation of cell size and chloroplast number in leaf mesophyll of rice. Plant Breeding 119, 531–533
Hayashida A, Takechi K, Sugiyama M, Kubo M, Itoh RD, Takio S, Fujita T, Hiwatashi Y, Hasebe M, Takano H. 2005. Isolation of mutant lines with decreased numbers of chloroplasts per cell from a tagged mutant library of the moss Physcomitrella patens . Plant Biology 7, 300–306 PubMed
Jin B, Wang L, Wang J, Jiang KZ, Wang Y, Jiang XX, Ni CY, Wang YL, Teng NJ. 2011. The effect of experimental warming on leaf functional traits, leaf structure and leaf biochemistry in Arabidopsis thaliana . BMC Plant Biology 11, 10. PubMed PMC
Kubínová L. 1991. Stomata and mesophyll characteristics of barley leaf as affected by light—stereological analysis. Journal of Experimental Botany 42, 995–1001
Kubínová L. 1993. Recent stereological methods for the measurement of leaf anatomical characteristics: estimation of volume density, volume and surface area. Journal of Experimental Botany 44, 165–173
Kubínová L. 1994. Recent stereological methods for measuring leaf anatomical characteristics: estimation of the number and sizes of stomata and mesophyll cells. Journal of Experimental Botany 45, 119–127
Kubínová L, Janáček J, Krekule I. 2002. Stereological methods for estimating geometrical parameters of microscopical structure studied by three-dimensional microscopical techniques. In: Diaspro A, ed. Confocal and two-photon microscopy, New York: Wiley-Liss
Lamppa GK, Elliot LV, Bendich AJ. 1980. Changes in chloroplast number during pea leaf development—an analysis of a protoplast population. Planta 148, 437–443 PubMed
Lhotáková Z, Albrechtová J, Janáček J, Kubínová L. 2008. Advantages and pitfalls of using free-hand sections of frozen needles for three-dimensional analysis of mesophyll by stereology and confocal microscopy. Journal of Microscopy 232, 56–63 PubMed PMC
Marrison JL, Rutherford SM, Robertson EJ, Lister C, Dean C, Leech RM. 1999. The distinctive roles of five different ARC genes in the chloroplast division process in Arabidopsis. Plant Journal 18, 651–662 PubMed
Marsaglia G. 2006. Ratios of normal variables. Journal of Statistical Software 16, 1–10
Maslova TG, Mamushina NS, Sherstneva OA, Bubolo LS, Zubkova EK. 2009. Seasonal structural and functional changes in the photosynthetic apparatus of evergreen conifers. Russian Journal of Plant Physiology 56, 607–615
Meyer R, Yuan J, Afzal J, Iqbal MJ, Zhu MX, Garvey G, Lightfoot DA. 2006. Identification of Gsr1 in Arabidopsis thaliana: a locus inferred to regulate gene expression in response to exogenous glutamine. Euphytica 151, 291–302
Miyazawa SI, Terashima I. 2001. Slow development of leaf photosynthesis in an evergreen broad-leaved tree, Castanopsis sieboldii: relationships between leaf anatomical characteristics and photosynthetic rate. Plant, Cell & Environment 24, 279–291
Mochizuki A, Sueoka N. 1955. Genetic studies on the number of plastid in stomata. I. Effect of autopolyploidy in sugar beets. Cytologia 20, 358–366
Molin WT, Meyers SP, Baer GR, Schrader LE. 1982. Ploidy effects in isogenic populations of alfalfa. 2. Photosynthesis, chloroplast number, ribulose-1,5-bisphosphate carboxylase, chlorophyll, and DNA in protoplasts. Plant Physiology 70, 1710–1714 PubMed PMC
Mozafari J, Wolyn DJ, AliKhan ST. 1997. Chromosome doubling via tuber disc culture in dihaploid potato as determined by confocal microscopy. Plant Cell Reports 16, 329–333 PubMed
Nicholson GG. 1981. The use of chloroplast numbers in guard cells as a means of distinguishing the chromosome races of Ranunculus ficaria L. Annals of Botany 48, 909–913
O’Brian TP, McCully ME. 1981. The study of plant structure: principles and selected methods. Melbourne, Australia: Termarcarphi Pty Ltd
Oguchi R, Hikosaka K, Hirose T. 2005. Leaf anatomy as a constraint for photosynthetic acclimation: differential responses in leaf anatomy to increasing growth irradiance among three deciduous trees. Plant, Cell & Environment 28, 916–927
Pazourek J. 1966. Anatomical gradients. Acta Universitatis Carolinae—Biologica , Suppl. 1/2, 19–25
Possingham JV, Saurer W. 1969. Changes in chloroplast number per cell during leaf development in spinach (Spinacea oleracea). Planta 86, 186–194 PubMed
Possingham JV, Smith JW. 1972. Factors affecting chloroplast replication in spinach. Journal of Experimental Botany 23, 1050–1059
Possingham JV. 1980. Plastid replication and development in the life-cycle of higher-plants. Annual Review of Plant Physiology and Plant Molecular Biology 31, 113–129
Pyke KA, Leech RM. 1991. Rapid image analysis screening procedure for identifying chloroplast number mutants in mesophyll cells of Arabidopsis thaliana (L.) Heynh. Plant Physiology 96, 1193–1195 PubMed PMC
Pyke KA, Leech RM. 1992. Chloroplast division and expansion is radically altered by nuclear mutations in Arabidopsis thaliana . Plant Physiology 99, 1005–1008 PubMed PMC
Qin X, Rotino GL. 1995. Chloroplast number in guard cells as ploidy indicator of in vitro-grown androgenic pepper plantlets. Plant Cell Tissue and Organ Culture 41, 145–149
Sam O, Ramirez C, Coronado MJ, Testillano PS, Risueno MC. 2003. Changes in tomato leaves induced by NaCl stress: leaf organization and cell ultrastructure. Biologia Plantarum 47, 361–366
Sari N, Abak K, Pitrat M. 1999. Comparison of ploidy level screening methods in watermelon: Citrullus lanatus (Thunb.) Matsum. and Nakai. Scientia Horticulturae 82, 265–277
Simon UK, Polanschütz LM, Koffler BE, Zechmann B. 2013. High resolution imaging of temporal and spatial changes of subcellular ascorbate, glutathione and H2O2 Distribution during Botrytis cinerea infection in Arabidopsis. PLoS ONE 8, 1–11 PubMed PMC
Soukupová J, Cvikrová M, Albrechtová J, Rock BN, Eder J. 2000. Histochemical and biochemical approaches to the study of phenolic compounds and peroxidases in needles of Norway spruce (Picea abies). New Phytologist 146, 403–414
Sterio DC. 1984. The unbiased estimation of number and sizes of arbitrary particles using the disector. Journal of Microscopy 134, 127–136 PubMed
Stettler M, Eicke S, Mettler T, Messerli G, Hortensteiner S, Zeeman SC. 2009. Blocking the metabolism of starch breakdown products in Arabidopsis leaves triggers chloroplast degradation. Molecular Plant 2, 1233–1246 PubMed PMC
Sung FJM, Chen JJ. 1989. Changes in photosynthesis and other chloroplast traits in lanceolate leaflet isoline of soybean. Plant Physiology 90, 773–777 PubMed PMC
Teng NJ, Wang J, Chen T, Wu XQ, Wang YH, Lin JX. 2006. Elevated CO2 induces physiological, biochemical and structural changes in leaves of Arabidopsis thaliana . New Phytologist 172, 92–103 PubMed
Terashima I, Hanba YT, Tholen D, Niinemets U. 2011. Leaf functional anatomy in relation to photosynthesis. Plant Physiology 155, 108–116 PubMed PMC
Tomori Z, Krekule I, Kubínová L. 2001. DISECTOR program for unbiased estimation of particle number, numerical density and mean volume. Image Analysis & Stereology 20, 119–130
Tymms MJ, Scott NS, Possingham JV. 1983. DNA content of Beta vulgaris chloroplasts during leaf cell expansion. Plant Physiology 71, 785–788 PubMed PMC
Urban O, Janouš D, Pokorný R, Marková I, Pavelka M, Fojtík Z, Šprtová M, Kalina J, Marek MV. 2001. Glass domes with adjustable windows: a novel technique for exposing juvenile forest stands to elevated CO2 concentration. Photosynthetica 39, 395–401
Wang XZ, Anderson OR, Griffin KL. 2004. Chloroplast numbers, mitochondrion numbers and carbon assimilation physiology of Nicotiana sylvestris as affected by CO2 concentration. Environmental and Experimental Botany 51, 21–31
Weibel ER. 1979. Practical methods for biological morphometry. In: Stereological methods , vol. 1 New York: Academic Press, 1–415
Xu CY, Salih A, Ghannoum O, Tissue DT. 2012. Leaf structural characteristics are less important than leaf chemical properties in determining the response of leaf mass per area and photosynthesis of Eucalyptus saligna to industrial-age changes in [CO2] and temperature. Journal of Experimental Botany 63, 5829–5841 PubMed
Yamasaki T, Kudoh T, Kamimura Y, Katoh S. 1996. A vertical gradient of the chloroplast abundance among leaves of Chenopodium album . Plant and Cell Physiology 37, 43–48
Zechmann B, Müller M, Zellnig G. 2003. Cytological modifications in zucchini yellow mosaic virus (ZYMV)-infected Styrian pumpkin plants. Archives of Virology 148, 1119–1133 PubMed