Long-term ecological consequences of forest fires in the continuous permafrost zone of Siberia

Abstract Wildfires are an important factor in controlling forest ecosystem dynamics across the circumpolar boreal zone. An improved understanding of their direct and indirect, short- to long-term impacts on vegetation cover and permafrost–vegetation coupling is particularly important to predict changes in carbon, nutrient and water cycles under projected climate warming. Here, we apply dendrochronological techniques on a multi-parameter dataset to reconstruct the effect of wildfires on tree growth and seasonal permafrost thaw depth in Central Siberia. Based on annually-resolved and absolutely dated information from 19 Gmelin larch (Larix gmelinii (Rupr.) Rupr.) trees and active soil layer thickness measurements, we find substantial stand-level die-off, as well as the removal of ground vegetation and the organic layer following a major wildfire in 1896. Reduced stem growth coincides with increased δ 13C in the cellulose of the surviving trees during the first decade after the wildfire, when stomatal conductance was reduced. The next six to seven decades are characterized by increased permafrost active soil layer thickness. During this period of post-wildfire ecosystem recovery, enhanced tree growth together with positive δ 13C and negative δ 18O trends are indicative of higher rates of photosynthesis and improved water supply. Afterwards, a thinner active soil layer leads to reduced growth because tree physiological processes become limited by summer temperature and water availability. Revealing long-term effects of forest fires on active soil layer thickness, ground vegetation composition and tree growth, this study demonstrates the importance of complex vegetation–permafrost interactions that modify the trajectory of post-fire forest recovery across much of the circumpolar boreal zone. To further quantify the influence of boreal wildfires on large-scale carbon cycle dynamics, future work should consider a wide range of tree species from different habitats in the high-northern latitudes.</jats:p

Radionuclide imaging of bone marrow disorders

Noninvasive imaging techniques have been used in the past for visualization the functional activity of the bone marrow compartment. Imaging with radiolabelled compounds may allow different bone marrow disorders to be distinguished. These imaging techniques, almost all of which use radionuclide-labelled tracers, such as 99mTc-nanocolloid, 99mTc-sulphur colloid, 111In-chloride, and radiolabelled white blood cells, have been used in nuclear medicine for several decades. With these techniques three separate compartments can be recognized including the reticuloendothelial system, the erythroid compartment and the myeloid compartment. Recent developments in research and the clinical use of PET tracers have made possible the analysis of additional properties such as cellular metabolism and proliferative activity, using 18F-FDG and 18F-FLT. These tracers may lead to better quantification and targeting of different cell systems in the bone marrow. In this review the imaging of different bone marrow targets with radionuclides including PET tracers in various bone marrow diseases are discussed

Neutrophil extracellular traps as an adhesion substrate for different tumor cells expressing RGD-binding integrins.

Neutrophil extracellular traps (NETs), in addition to their function as a host defense mechanism, play a relevant role in thrombus formation and metastatic dissemination of cancer cells. Here we screened different cancer cell lines endogenously expressing a variety of integrins for their ability to bind to NETs. To this end, we used NETs isolated from neutrophil-like cells as a substrate for adhesion assays of HT1080, U-87 MG, H1975, DU 145, PC-3 and A-431 cells. Levels of α5, αIIb, αv, β1, β3 and β5 chains were determined by western blot analysis in all cell lines and levels of whole integrins on the plasma membrane were assessed by fluorescence-activated cell sorting (FACS) analysis. We found that high levels of α5β1, αvβ3 and αvβ5 enhance cell adhesion to NETs, whereas low expression of α5β1 prevents cell attachment to NETs. Excess of cyclic RGD peptide inhibited cell adhesion to NETs by competing with fibronectin within NETs. The maximal reduction of such adhesion was similar to that obtained by DNase 1 treatment causing DNA degradation. Our findings indicate that NETs from neutrophil-like cells may be used as a substrate for large screening of the adhesion properties of cancer cells expressing a variety of RGD-binding integrins