In the present work we have functionally characterized these ligand binding regions. Similar to the wild type receptor, both regions bind TGF-2 with higher affinity than TGF-1. However, only the endoglin-related region increases the TGF-2 labeling of the TGF- type II receptor, the so-called "TGF- -presentation" function of the wild type receptor. Despite this preference, both regions as well as the wild type receptor mediate the TGF-2-dependent Smad2 phosphorylation, indicating that they can function indistinguishably as TGF--enhancing coreceptors. On the other hand, we found that the recently described ability of the wild type betaglycan to bind inhibin A is a property of the core protein that resides in the uromodulin-related region. Binding competition experiments indicate that this region binds inhibin and TGF- with the following relative affinities: TGF-2 > inhibin A > TGF-1. All together, the present results suggest that betaglycan ectodomain is endowed with two bona fide independent ligand binding domains that can perform specialized functions as co-receptors of distinct members of the TGF- superfamily. Transforming growth factor- (TGF-)1 is the prototype of a superfamily of growth factors involved in the regulation of cell proliferation, differentiation, and development (1, 2). TGF- signals through a complex of transmembrane serine/threonine kinase receptors, the TGF- type I and type II receptors. Ligand binding promotes the association between the type I and II receptors. In this complex, phosphorylation of the type I receptor kinase by the constitutively active type II receptor kinase results in its activation. Active type I receptor phosphorylates members of a novel family of transcriptional regulators, the Smads, which transduce the TGF- signal into the cell nucleus (3, 4).TGF- has two known co-receptors, betaglycan and endoglin, which are transmembrane glycoproteins with large extracellular regions that bind TGF- and small cytoplasmatic regions without any clearly identifiable signaling motif (5-8). Betaglycan is a membrane proteoglycan containing heparan and chondroitin sulfate chains whose core protein binds all three TGF- isoforms (9 -11). Betaglycan is capable of fine tuning the availability of TGF- to the signaling receptors, thereby determining the outcome of the TGF- stimulation (12, 13). This regulation is both positive and negative. Although the membrane-bound form of betaglycan increases the binding of TGF- to the signaling complex, the soluble form of betaglycan prevents this binding and therefore blocks the actions of TGF- (14). These effects are more dramatic for TGF-2, the isoform for which betaglycan has higher affinity (15-17). Expression of membrane betaglycan in cells that normally do not express this co-receptor increases their binding to TGF-2 and corrects for their low sensitivity to this TGF- isoform (18,19). Presumably, this effect is mediated by a TGF--induced "presentation complex" formed between membrane-bound betaglycan and the TGF- type II rece...
Betaglycan is an accessory receptor of members of the transforming growth factor-β (TGF-β) superfamily, which regulates their actions through ligand-dependent interactions with type II receptors. A natural soluble form of betaglycan is found in serum and extracellular matrices. Soluble betaglycan, prepared as a recombinant protein using the baculoviral expression system, inhibits the actions of TGF-β. Because of its potential use as an anti-TGF-β therapeutic agent, we have purified and characterized baculoviral recombinant soluble betaglycan. Baculoviral soluble betaglycan is a homodimer formed by two 110kDa monomers associated by non-covalent interactions. This protein is devoid of glycosaminoglycan chains, although it contains the serine residues, which, in vertebrate cells, are modified by these carbohydrates. On the other hand, mannose-rich carbohydrates account for approximately 20kDa of the mass of the monomer. End-terminal sequence analysis of the soluble betaglycan showed that Gly24 is the first residue of the mature protein. Similarly to the natural soluble betaglycan, baculoviral soluble betaglycan has an equilibrium dissociation constant (Kd) of 3.5nM for TGF-β1. Ligand competition assays indicate that the relative affinities of recombinant soluble betaglycan for the TGF-β isoforms are TGF-β2>TGF-β3>TGF-β1. The anti-TGF-β potency of recombinant soluble betaglycan invitro is 10-fold higher for TGF-β2 than for TGF-β1. Compared with a commercial pan-specific anti-TGF-β neutralizing antibody, recombinant soluble betaglycan is more potent against TGF-β2 and similar against TGF-β1. These results indicate that baculoviral soluble betaglycan has the biochemical and functional properties that would make it a suitable agent for the treatment of the diseases in which excess TGF-β plays a central physiopathological role.
SummaryBetaglycan is a co-receptor for members of the TGF-β superfamily. Mutagenesis has identified two ligand binding regions, one at the membrane-distal and the other at the membrane-proximal half of the betaglycan ectodomain. Here we show that partial plasmin digestion of soluble betaglycan produces two proteolysis-resistant fragments of 45 and 55 kDa, consistent with the predicted secondary structure, which indicates an intervening non-structured linker region separating the highly structured N-and C-terminal domains. Amino terminal sequencing indicates that the 45 and 55 kDa fragments correspond, respectively, to the membrane-distal and -proximal regions. Plasmin treatment of membrane betaglycan results in the production of equivalent proteolysis-resistant fragments. The 45 and 55 kDa fragments, as well as their recombinant soluble counterparts, Sol Δ10 and Sol Δ11, bind TGF-β, nonetheless, compared to intact soluble betaglycan, have severely diminished ability to block TGF-β activity. Surface plasmon resonance (SPR) analysis indicates that soluble betaglycan has K d s in the low nanomolar range for the three TGF-β isoforms, while those for Sol Δ10 and Sol Δ11 are 1 -2 orders of magnitude higher. SPR analysis further shows that the K d s of Sol Δ11 are not changed in the presence of Sol Δ10, indicating that the high affinity of soluble betaglycan is a consequence of tethering of the domains together. Overall, these results, suggest that betaglycan ectodomain exhibits a bi-lobular structure in which each lobule folds independently, binds TGF-β through distinct non-overlapping interfaces, and that linker modification may be an approach to improve soluble betaglycan's TGF-β neutralizing activity.Address correspondence to Jose-Luis Montiel, PhD, Av. Universidad 1001, Colonia Chamilpa, Cuernavaca, Morelos, 62209, México. Phone and fax: +(52) 77 73297000 ext. 3371. jlmontiel@uaem.mx. Supporting InformationThis manuscript presents biochemical evidence that betaglycan ectodomain is composed of two independently folded TGF-β binding domains. Determination of their TGF-β affinity binding constants indicate both of these domains are required for the high affinity TGF-β binding and the complete TGF-β neutralizing activity of the full-length soluble betaglycan. Supporting information can be found at http://pubs.acs.org. NIH Public Access Author ManuscriptBiochemistry. Author manuscript; available in PMC 2010 December 15. NIH-PA Author ManuscriptNIH-PA Author Manuscript NIH-PA Author ManuscriptBetaglycan (BG) is a membrane proteoglycan that serves as a co-receptor for diverse members of the TGF-β superfamily of autocrine and paracrine factors. These factors are involved in diverse biological functions that include, among others, embryonic development, cell differentiation and proliferation, control of the immune response and wound repair (1). BG binds TGF-β superfamily factors with a characteristic selectivity: TGF-β2 > TGF-β1 > inhibin A, and establishes ligand-dependent complexes with several type II receptors (2). Th...
Cardiovascular diseases (CVD) (such as occlusion of the coronary arteries, hypertensive heart diseases and strokes) are diseases that generate thousands of patients with a high mortality rate worldwide. Many of these cardiovascular pathologies, during their development, generate a state of oxidative stress that leads to a deterioration in the patient’s conditions associated with the generation of reactive oxygen species (ROS) and reactive nitrogen species (RNS). Within these reactive species we find superoxide anion (O2•–), hydroxyl radical (•OH), nitric oxide (NO•), as well as other species of non-free radicals such as hydrogen peroxide (H2O2), hypochlorous acid (HClO) and peroxynitrite (ONOO–). A molecule that actively participates in counteracting the oxidizing effect of reactive species is reduced glutathione (GSH), a tripeptide that is present in all tissues and that its synthesis and/or regeneration is very important to be able to respond to the increase in oxidizing agents. In this review, we will address the role of glutathione, its synthesis in both the heart and the liver, and its importance in preventing or reducing deleterious ROS effects in cardiovascular diseases.
SummaryTransforming growth factor-beta (TGF-β β β β ) and prostaglandins (PG) regulate the cell-mediated immune response, so it has been proposed that they affect the progression of pulmonary tuberculosis. Here we report that the administration of soluble betaglycan, a potent TGF-β β β β antagonist, and niflumic acid, a PG synthesis inhibitor, during the chronic phase of experimental murine tuberculosis enhanced Th1 and decreased Th2 cytokines, increased the expression of iNOS and reduced pulmonary inflammation, fibrosis and bacillary load. This immunotherapeutic approach resulted in significant control of the disease comparable to that achieved by anti-microbial treatment alone. Importantly, the combination of immunotherapy and anti-microbials resulted in an accelerated clearance of bacilli from the lung. These results confirm that TGF-β β β β and PG have a central pathophysiological role in the progression of pulmonary tuberculosis in the mouse and suggest that the addition of immunotherapy to conventional anti-microbial drugs might result in improved treatment of the disease.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.