Induction Of Protease Inhibitors Research Articles

Rosellinia necatrix infection induces differential gene expression between tolerant and susceptible avocado rootstocks.

Rosellinia necatrix is the causal agent of avocado white root rot (WRR). Control of this soil-borne disease is difficult, and the use of tolerant rootstocks may present an effective method to lessen its impact. To date, no studies on the molecular mechanisms regulating the avocado plant response towards this pathogen have been undertaken. To shed light on the mechanisms underpinning disease susceptibility and tolerance, molecular analysis of the gene’s response in two avocado rootstocks with a contrasting disease reaction was assessed. Gene expression profiles against R. necatrix were carried out in the susceptible ‘Dusa’ and the tolerant selection BG83 avocado genotypes by micro-array analysis. In ‘Dusa’, the early response was mainly related to redox processes and cell-wall degradation activities, all becoming enhanced after disease progression affected photosynthetic capacity, whereas tolerance to R. necatrix in BG83 relied on the induction of protease inhibitors and their negative regulators, as well as genes related to tolerance to salt and osmotic stress such as aspartic peptidase domain-containing proteins and gdsl esterase lipase proteins. In addition, three protease inhibitors were identified, glu protease, trypsin and endopeptidase inhibitors, which were highly overexpressed in the tolerant genotype when compared to susceptible ‘Dusa’, after infection with R. necatrix, reaching fold change values of 52, 19 and 38, respectively. The contrasting results between ‘Dusa’ and BG83 provide new insights into the different mechanisms involved in avocado tolerance to Phytophthora cinnamomi and R. necatrix, which are consistent with their biotrophic and necrotrophic lifestyles, respectively. The differential induction of genes involved in salt and osmotic stress in BG83 could indicate that R. necatrix penetration into the roots is associated with osmotic effects, suggesting that BG83’s tolerance to R. necatrix is related to the ability to withstand osmotic imbalance. In addition, the high expression of protease inhibitors in tolerant BG83 compared to susceptible ‘Dusa’ after infection with the pathogen suggests the important role that these proteins may play in the defence of avocado rootstocks against R. necatrix.

Human adipose-derived mesenchymal stem cell spheroids improve recovery in a mouse model of elastase-induced emphysema.

Emphysema, a pathologic component of the chronic obstructive pulmonary disease, causes irreversible destruction of lung. Many researchers have reported that mesenchymal stem cells can regenerate lung tissue after emphysema. We evaluated if spheroid human adipose-derived mesenchymal stem cells (ASCs) showed greater regenerative effects than dissociated ASCs in mice with elastase-induced emphysema. ASCs were administered via an intrapleural route. Mice injected with spheroid ASCs showed improved regeneration of lung tissues, increased expression of growth factors such as fibroblast growth factor-2 (FGF2) and hepatocyte growth factor (HGF), and a reduction in proteases with an induction of protease inhibitors when compared with mice injected with dissociated ASCs. Our findings indicate that spheroid ASCs show better regeneration of lung tissues than dissociated ACSs in mice with elastase-induced emphysema.

Drought stress in tomato increases the performance of adapted and non-adapted strains of Tetranychus urticae

The performance of the two-spotted spider mite, Tetranychus urticae Koch, on plants depends on the rate of adaptation of mite populations to each particular host and can be influenced by environmental conditions. We have tested the effects of drought stress, caused by water deficiency, in the interaction of tomato plants with tomato adapted (TA) and tomato non-adapted (TNA) strains of T. urticae. Our data revealed that mite performance was enhanced for the TA strain when reared on drought-stressed tomato plants, rising population growth and leaf damage. Population growth in the case of the TNA strain was negative, but they laid more eggs and the number of mobile forms was higher on drought-stressed tomato plants than on control plants. Water stress resulted in tomato plants with increased concentrations of essential amino acids and free sugars, improving the nutritional value of drought-stressed tomato plants for T. urticae. Mite infestation alone had almost no effect on the nutritional composition of tomato leaves, with the exception of an increase of free sugars. Tomato plant defense proteins were induced by both drought stress and mite infestation. However, the induction of protease inhibitors was higher in tomatoes exposed to mites from the TNA strain than in tomatoes that were fed upon by mites from the TA strain. The better performance of the TA strain could be associated to both changes in the digestive (cysteine and aspartyl protease and α-amylase activities) and detoxification (esterase activity) physiology of the mites and the attenuation of some of the plant defenses (protease inhibitors). Taken together, our results suggest that drought stress might favor outbreaks of T. urticae on tomato, by enhancing population growth of adapted populations and increasing the suitability of tomato as a host for non-adapted ones.

Systemin, Hydroxyproline-Rich Systemin and the Induction of Protease Inhibitors

Systemin, an 18-amino acid signaling peptide isolated from tomato leaves, has been found to be an integral component of the jasmine acid signaling pathway, leading to the synthesis of protease inhibitors (PIs). The discovery of systemin has led to a search for other peptide signals involved in defense in the Solanaceae and in other plant families. A new class of peptides having similar signaling properties but little sequence homology to systemin have been found and termed hydroxyproline-rich glycopeptide systemins (HypSys). These small (18-20 amino acids) glycopeptides, like systemin, are derived from larger precursor proteins (proHypSys) and until recently were thought to function only in protection from herbivore attack. However, HypSys peptides isolated from petunia induced the defensin gene, known for its involvement in pathogen defense. More recently, a HypSys glycopeptide was isolated from sweet potato, a member of the Convolvulaceae family and found to induce the sporamin gene which codes for the major storage protein in tubers with trypsin inhibitor activity. These recent discoveries expand the function and range of the HypSys family of glycopeptides and establish these unique inducible signaling molecules as potential components of defense pathways throughout the Eudicots. Herein we review the signaling and structural properties of systemin and the HypSys glycopeptides and their roles in the induction of PIs.

Shear stress‐induced Ets‐1 modulates protease inhibitor expression in microvascular endothelial cells

Elevated shear stress within the skeletal muscle microvasculature is implicated in the induction of a longitudinal splitting form of angiogenesis, which is characterized by the lack of basement membrane breakage. We investigated whether the transcriptional regulator, Ets-1, is responsive to changes in hemodynamic forces and if so, whether Ets-1 controls microvascular endothelial cell integrity by inducing the expression of inhibitors of matrix degrading proteases. Rats were treated with prazosin for 2, 4, and 7 days to increase in microvascular shear stress in hindlimb skeletal muscles. In complimentary in vitro experiments, rat microvascular skeletal muscle endothelial cells were exposed to laminar shear stress (15 dyne/cm(2)) for 0.5, 2, and 24 h. TaqMan PCR analysis of laser microdissected capillaries isolated from EDL muscles demonstrated transient (after 2 days) induction of Ets-1 gene expression. In cultured cells, a transient up-regulation of Ets-1 mRNA was observed after 2 h shear stimulation, accompanied by increased phosphorylation of Ets-1 and enhanced Ets-1 DNA binding activity. This response was modulated by ERK1/2 and p38 MAP kinases, but was not dependent on NOS or COX-2 activity. PAI-1, TIMP-1 and TIMP-3 mRNA were elevated significantly in prazosin treated EDL, and in response to shear stimulation in vitro. In cultured endothelial cells, Ets-1 RNA interference abolished the shear-induced increases in Ets-1, PAI-1, TIMP-1, and TIMP-3 mRNA expression. These results suggest that enhanced laminar shear stress may act to preserve the integrity of microvascular walls in part through Ets-1-dependent induction of protease inhibitors.

The role of TGF-β signaling in myocardial infarction and cardiac remodeling

Transforming Growth Factor (TGF)-beta is markedly induced and rapidly activated in the infarcted myocardium. However, understanding of the exact role of TGF-beta signaling in the infarcted and remodeling heart has been hampered by the complex and unusual biology of TGF-beta activation and by the diversity of its effects eliciting multiple, and often opposing cellular responses. Experimental studies suggest that TGF-beta signaling may be crucial for repression of inflammatory gene synthesis in healing infarcts mediating resolution of the inflammatory infiltrate. In addition, TGF-beta may play an important role in modulating fibroblast phenotype and gene expression, promoting extracellular matrix deposition in the infarct by upregulating collagen and fibronectin synthesis and by decreasing matrix degradation through induction of protease inhibitors. TGF-beta is also a key mediator in the pathogenesis of hypertrophic and dilative ventricular remodeling by stimulating cardiomyocyte growth and by inducing interstitial fibrosis. In this review we summarize the current knowledge on the role of TGF-beta in infarct healing and cardiac remodeling.

Structural requirements for biologically active jasmonates: Induction of protease inhibitors and cotyledon senescence

Methyl jasmonate and jasmonate isomers were resolved for studies in stereoselectivity of biological action. Chemical modifications included fluorination at the chiral C7 carbon, trifluorination at the C12 of the pentenyl sidechain, shortening of this pentenyl to a butenyl moiety, and synthesis of the (+) and (–)-epi-methyl jasmonates. The effects of these modifications and stereospecificity were monitored using three assays: proteinase inhibitor II promoter driving the reporter β-glucuronidase; endogenous trypsin proteinase inhibitor induction; and sunflower cotyledon senescence induction. The methyl esters were more active than the corresponding acids, the R absolute configuration at C3 was most effective in all assays, fluorination at C7 abolished activity in the proteinase inhibitor assays, and the trifluorination at C12 or shortening to a butenyl did not alter activity relative to the active (–)- methyl jasmonate, but both of these latter modifications revealed a delayed response in the senescence conductivity measures.