Seed coat development in explosively dispersed seeds of Cardamine hirsuta

Background and Aims Seeds are dispersed by explosive coiling of the fruit valves in Cardamine hirsuta. This rapid coiling launches the small seeds on ballistic trajectories to spread over a 2 m radius around the parent plant. The seed surface interacts with both the coiling fruit valve during launch and subsequently with the air during flight. We aim to identify features of the seed surface that may contribute to these interactions by characterizing seed coat differentiation. Methods Differentiation of the outermost seed coat layers from the outer integuments of the ovule involves dramatic cellular changes that we characterize in detail at the light and electron microscopical level including immunofluorescence and immunogold labelling. Key Results We found that the two outer integument (oi) layers of the seed coat contributed differently to the topography of the seed surface in the explosively dispersed seeds of C. hirsuta vs. the related species Arabidopsis thaliana where seed dispersal is non-explosive. The surface of A. thaliana seeds is shaped by the columella and the anticlinal cell walls of the epidermal oi2 layer. In contrast, the surface of C. hirsuta seeds is shaped by a network of prominent ridges formed by the anticlinal walls of asymmetrically thickened cells of the sub-epidermal oi1 layer, especially at the seed margin. Both the oi2 and oi1 cell layers in C. hirsuta seeds are characterized by specialized, pectin-rich cell walls that are deposited asymmetrically in the cell. Conclusions The two outermost seed coat layers in C. hirsuta have distinct properties: the sub-epidermal oi1 layer determines the topography of the seed surface, while the epidermal oi2 layer accumulates mucilage. These properties are influenced by polar deposition of distinct pectin polysaccharides in the cell wall. Although the ridged seed surface formed by oi1 cell walls is associated with ballistic dispersal in C. hirsuta, it is not restricted to explosively dispersed seeds in the Brassicaceae.

Topological Order: From Long-Range Entangled Quantum Matter to a Unified Origin of Light and Electrons

We review the progress in the last 20–30 years, during which we discovered that there are many new phases of matter that are beyond the traditional Landau symmetry breaking theory. We discuss new “topological” phenomena, such as topological degeneracy that reveals the existence of those new phases—topologically ordered phases. Just like zero viscosity defines the superfluid order, the new “topological” phenomena define the topological order at macroscopic level. More recently, we found that at the microscopical level, topological order is due to long-range quantum entanglements. Long-range quantum entanglements lead to many amazing emergent phenomena, such as fractional charges and fractional statistics. Long-range quantum entanglements can even provide a unified origin of light and electrons; light is a fluctuation of long-range entanglements, and electrons are defects in long-range entanglements.

OPTIMAL RESOLUTION FOR AUTOMATIC QUANTIFICATION OF BLOOD VESSELS ON DIGITIZED IMAGES OF THE WHOLE CANCER SECTION

Discrepancies concerning the prognostic significance of cancer vascularization can be partly explained by biases due to quantification protocols. We recently recommended a swift, inexpensive and automatic analysis of 2,700 dpi slide scanner images of the whole immunostained sections. Another team, proposed, quite at the same time, to work at 4,000 dpi. The aim of the present paper is to check if information contained in images scanned at 2,700 and 4,000 dpi are relevant and equivalent, when compared to the low magnification of the microscope, in order to propose the best compromise between precision and time expense. To evaluate precisely the amount of information gained or lost according to the resolution used, we compared the number and size of blood vessel profiles, manually detected, on twenty one Hodgkin lymphoma acquired with a scanner (2,700 and 4,000 dpi) and with a microscope (16,000 dpi). Results obtained at 4,000 dpi were equivalent to the estimation performed at microscopical level either by a biologist or a pathologist, while tiny vessels were lost at 2,700 dpi. Scanning whole histological sections at 4,000 dpi provides a relevant method for evaluating tumour vascularization, which can be easily automated and standardized.

Seminal Phagocytes Detection at Light-Microscopy Level using Three Different Techniques

The phagocytes are normally present in the conective tissue at different organs, and their number increased in immunological or inflammatory processes. In these cases, they are present too in corporal fluids.The presence of phagocytes in semen was referred by several authors, but that phenomenon has not been suficiently analysed. At smear Papanicolaou stained analysis, the seminal phagocytes can be inadverted thus, their relationship to the male infertility or another reproductive tract pathology can not be established.In this study we implemented three techniques to detect the presence of phagocytes in semen of 28 infertile patients: Myeloperoxidase for polymorphonuclears (leukocyte), Neutral red for macrophages and the semithin sections analysis at light microscopical level of the seminal pellet obtained by centrifugation and included in epoxyresin.

Immunoelectron characterisation of the inter-endothelial junctions of human term placenta

The molecular constituents of the paracellular clefts in human placental microvessels were investigated using antibodies against PECAM-1, pan-cadherin, A-CAM (N-cadherin), cadherin-5 and two types of integrins (those recognised by antibodies to the beta 1 chain and alpha v beta 3). Ultrastructural localisation of these molecules in ultrathin frozen sections of human term placentae was attempted using colloidal gold immunocytochemistry, after establishing their presence by indirect immunofluorescence. At the light microscopical level, the endothelial paracellular clefts were found to be immunoreactive to the antibodies against PECAM-1, cadherin-5 and pan-cadherin, but not the integrins. The latter showed diffuse distribution in the endothelium and in the abluminal interstitial space. PECAM-1 and pan-cadherin were also seen in the cytoplasm and luminal surface of the endothelium. Immunoelectron studies revealed that the cadherins and PECAM-1 were present in the wide regions of the paracellular clefts, but not in tight junctional regions. Using immunocytochemistry, these wide junctional areas were found to be associated with the cytoskeletal linking molecules vinculin and alpha-actinin. These regions may therefore contain adherens-type junctions. Cadherin-5, localised by two different monoclonal antibodies, 7B4 and TEA, was the only antigen which was cleft-specific, the others also being seen in the cytoplasm of the microvascular endothelium. Cadherin-5 and pan-cadherin were co-localised in the same wide junction, but were usually seen to occupy different microdomains of, and different wide zones of, the same cleft. The cell adhesion molecules localised in the paracellular wide junctions of the human placental microvessels may play a role in maintaining the intercellular spacing between endothelial cells, and may be part of a paracellular “fibre matrix” with permeability-restricting properties.