Stem Cell Basis for Fractal Patterns: Axillary Meristem Initiation

Whereas stem cell lineages are of enormous importance in animal development, their roles in plant development have only been appreciated in recent years. Several specialized lineages of stem cells have been identified in plants, such as meristemoid mother cells and vascular cambium, as well as those located in the apical meristems. The initiation of axillary meristems (AMs) has recently gained intensive attention. AMs derive from existing stem cell lineages that exit from SAMs and define new growth axes. AMs are in fact additional rounds of SAMs, and display the same expression patterns and functions as the embryonic SAM, creating a fractal branching pattern. Their formation takes place in leaf-meristem boundaries and mainly comprises two key stages. The first stage is the maintenance of the meristematic cell lineage in an undifferentiated state. The second stage is the activation, proliferation, and re-specification to form new stem cell niches in AMs, which become the new postembryonic “fountain of youth” for organogenesis. Both stages are tightly regulated by spatially and temporally interwound signaling networks. In this mini-review, I will summarize the most up-to-date understanding of AM establishment and mainly focus on how the leaf axil meristematic cell lineage is actively maintained and further activated to become CLV3-expressed stem cells, which involves phytohormonal cascades, transcriptional regulations, epigenetic modifications, as well as mechanical signals.

Morpho-Histological and Cytological Study on Meristematic Nodule Induction and Shoot Organogenesis in Paeonia Ostii ‘Feng Dan’

This is the first report concerning the sequence of morpho-histological and cytological events occurring during organogenesis from cotyledon-derived meristematic nodules (MNs) in Paeonia ostii ‘Feng Dan’. Sections were made and studies were carried out with dissecting microscope, light microscope, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) observation. Histological studies revealed a complex developmental process of morphogenesis that including five stages: (1) callus originated from cell division in both cambial and cortical regions, and type I - yellow compact callus with densely arranged clumps were identified as embryogenic callus. (2) pre-nodular structure consisted of organization center (a central area of vascularization surrounded by meristematic cell layers) and an epidermis-like layer; (3) independent MNs comprised of organization center, a cortical-like area of parenchymatous cells and an epidermal-like area; (4) nodular clusters displayed vigorously internal meristematic cell division and generated a relative movement towards the nodules periphery, establishing vascular connection with primordia; (5) successive new elongated shoots with complete vascular system and axillary bud primordia were developed. SEM observations showed three types of extracellular matrix (ECM), a smooth membranous layer, fibrillar structures and granular mucilage-like secretions on embryogenic callus, and recorded its dynamic morphological changes. Ultrastructural analysis revealed striking changes of chloroplast morphology and starch content during MNs morphogenesis. This study allows a better understanding of in vitro regeneration via MN culture and provides references for protocol optimization and genetic transformation.

Preventive efficiency of Cornelian cherry (Cornus mas L.) fruit extract in diniconazole fungicide-treated Allium cepa L. roots

Cornelian cherry (Cornus mas L.) is a medicinal plant with antioxidant-rich fruits. Diniconazole, a broad-spectrum fungicide, is employed extensively. The present study was designed to evaluate the preventive efficiency of C. mas fruit extract (CME) against the toxic effects of diniconazole on a model organism, Allium cepa L. For this aim, physiological, cytogenetic and biochemical parameters as well as the meristematic cell damages were investigated in A. cepa treated with diniconazole and C. mas extract. A. cepa bulbs were divided into six groups which were treated with tap water, 0.5 g/L CME, 1.0 g/L CME, 100 mg/L diniconazole, 0.5 g/L CME + 100 mg/L diniconazole and 1.0 g/L CME + 100 mg/L diniconazole, respectively. Diniconazole application caused a significant reduction in germination percentage, root elongation and total weight gain. Mitotic index decreased, while chromosomal aberrations increased following diniconazole application. Diniconazole caused significant rises in malondialdehyde content and the total activities of superoxide dismutase and catalase enzymes. The meristematic cell damages induced by diniconazole were indistinct transmission tissue, epidermis cell deformation, thickening of the cortex cell wall and flattened cell nucleus. Aqueous C. mas extracts induced a dose-dependent prevention and amelioration in all damages arisen from diniconazole application.

Biotransformation of 4-methylcoumarins by cambial meristematic cells of Camptotheca acuminata

Cambial meristematic cell (CMC) suspension cultures were investigated as a new biotransformation system for the first time.

Cytokinins regulate root growth through its action on meristematic cell proliferation but not on the transition to differentiation

Contrary to the wide-spread view that cytokinins change the rate of root growth and meristem size by regulating the cell transition to elongation (differentiation), our data showed that cytokinins affected the cell cycle duration in the meristem. The rate of meristematic cell transition to elongation itself is regulated by two groups of independent processes, through influence on (i) the life-span of cells in the meristem, and (ii) the cell proliferation rate in the meristem. Trans-zeatin slows down the root growth rate and the cell transition to elongation as a result of prolongation of mitotic cycles. The life-span of cells in the meristem does not change. The number of meristematic cells in one file decreases due to inhibition of cell proliferation but not to an acceleration of cell transition to elongation. Roots of triple mutant ipt3ipt5ipt7, in which cytokinin synthesis is slowed down, behave in an opposite way such that the rate of cell transition to elongation and cell proliferation is speeded up. Their peculiarity is that the life-span of cells in meristem becomes shorter than in control roots. In both cases, a change in concentration of endogenous cytokinin or in its signalling are associated with a change in mitotic cycle duration.