TY - JOUR
T1 - Characterization of polarity development through 2- and 3-D imaging during the initial phase of microspore embryogenesis in Brassica napus L.
AU - Dubas, E.
AU - Custers, J.
AU - Kieft, H.
AU - Wedzony, M.
AU - van Lammeren, A.A.M.
PY - 2014
Y1 - 2014
N2 - Isolated microspores of B. napus in culture change
their developmental pathway from gametophytic to sporophytic
and form embryo-like structures (ELS) upon prolonged heat
shock treatment (5 days at 32 °C). ELS express polarity during
the initial days of endosporic development. In this study, we
focussed on the analysis of polarity development of ELS
without suspensor. Fluorescence microscopy and 3-D confocal
laser scanning microscopy (CLSM) without tissue interfering
enabled us to get a good insight in the distribution of nuclei,
mitochondria and endoplasmic reticulum(ER), the architecture
of microtubular (MT) cytoskeleton and the places of 5-bromo-
2'-deoxy-uridine (BrdU) incorporation in successive stages of microspore embryogenesis. Scanning electron microscopy
(SEM) analysis revealed, for the first time, the appearance of
a fibrillar extracellular matrix-like structure (ECM-like structure)
in androgenic embryos without suspensor. Two types of
endosporic development were distinguished based upon the
initial location of the microspore nucleus. The polarity of
dividing and growing cells was recognized by the differential
distributions of organelles, by the organization of the MT
cytoskeleton and by the visualization of DNA synthesis in
the cell cycle. The directional location of nuclei, ER, mitochondria
and starch grains in relation to theMTs configurations
were early polarity indicators. Both exine rupture and ECMlike
structure on the outer surfaces of ELS are supposed to
stabilize ELS's morphological polarity. As the role of cell
polarity during early endosporic microspore embryogenesis
in apical–basal cell fate determination remains unclear, microspore
culture system provides a powerful in vitro tool for
studying the developmental processes that take place during
the earliest stages of plant embryogenesis.
AB - Isolated microspores of B. napus in culture change
their developmental pathway from gametophytic to sporophytic
and form embryo-like structures (ELS) upon prolonged heat
shock treatment (5 days at 32 °C). ELS express polarity during
the initial days of endosporic development. In this study, we
focussed on the analysis of polarity development of ELS
without suspensor. Fluorescence microscopy and 3-D confocal
laser scanning microscopy (CLSM) without tissue interfering
enabled us to get a good insight in the distribution of nuclei,
mitochondria and endoplasmic reticulum(ER), the architecture
of microtubular (MT) cytoskeleton and the places of 5-bromo-
2'-deoxy-uridine (BrdU) incorporation in successive stages of microspore embryogenesis. Scanning electron microscopy
(SEM) analysis revealed, for the first time, the appearance of
a fibrillar extracellular matrix-like structure (ECM-like structure)
in androgenic embryos without suspensor. Two types of
endosporic development were distinguished based upon the
initial location of the microspore nucleus. The polarity of
dividing and growing cells was recognized by the differential
distributions of organelles, by the organization of the MT
cytoskeleton and by the visualization of DNA synthesis in
the cell cycle. The directional location of nuclei, ER, mitochondria
and starch grains in relation to theMTs configurations
were early polarity indicators. Both exine rupture and ECMlike
structure on the outer surfaces of ELS are supposed to
stabilize ELS's morphological polarity. As the role of cell
polarity during early endosporic microspore embryogenesis
in apical–basal cell fate determination remains unclear, microspore
culture system provides a powerful in vitro tool for
studying the developmental processes that take place during
the earliest stages of plant embryogenesis.
KW - nuclear-dna synthesis
KW - cv topas
KW - extracellular-matrix
KW - sporophytic development
KW - cultured microspores
KW - actin-filament
KW - heat-shock
KW - in-vitro
KW - induction
KW - pollen
U2 - 10.1007/s00709-013-0530-y
DO - 10.1007/s00709-013-0530-y
M3 - Article
SN - 0033-183X
VL - 251
SP - 103
EP - 113
JO - Protoplasma
JF - Protoplasma
IS - 1
ER -