RESUMEN
Two genes, TSC1 and TSC2, have been shown to be responsible for tuberous sclerosis (TSC). The detection of loss of heterozygosity of TSC1 or TSC2 in hamartomas, the growths characteristically occurring in TSC patients, suggested a tumor suppressor function for their gene products hamartin and tuberin. Studies analyzing ectopically modulated expression of TSC2 in human and rodent cells together with the finding that a homolog of TSC2 regulates the Drosophila cell cycle suggest that TSC is a disease of proliferation/cell cycle control. We discuss this question including very recent data obtained from analyzing mice expressing a modulated TSC2 transgene, and from studying the effects of deregulated TSC1 expression. Elucidation of the cellular functions of these proteins will form the basis of a better understanding of how mutations in these genes cause the disease and for the development of new therapeutic strategies.
Asunto(s)
Ciclo Celular/genética , División Celular/genética , Proteínas de Drosophila , Genes Supresores de Tumor , Proteínas/fisiología , Proteínas Represoras/fisiología , Esclerosis Tuberosa/genética , Proteínas Supresoras de Tumor , Transporte Activo de Núcleo Celular , Animales , Carcinoma de Células Renales/genética , Compartimento Celular , Proteínas de Ciclo Celular/genética , Proteínas de Ciclo Celular/metabolismo , Proteínas de Ciclo Celular/fisiología , Tamaño de la Célula/genética , Cromosomas Humanos Par 16/genética , Cromosomas Humanos Par 9/genética , Inhibidor p27 de las Quinasas Dependientes de la Ciclina , Drosophila melanogaster/citología , Drosophila melanogaster/genética , Genes Dominantes , Hamartoma/genética , Humanos , Proteínas de Insectos/genética , Proteínas de Insectos/fisiología , Neoplasias Renales/genética , Pérdida de Heterocigocidad , Sustancias Macromoleculares , Proteínas/genética , Ratas , Ratas Mutantes , Proteínas Represoras/genética , Proteína 1 del Complejo de la Esclerosis Tuberosa , Proteína 2 del Complejo de la Esclerosis TuberosaRESUMEN
The transcription factors c-Myc and E2F-1 have been shown to harbour both mitogenic and apoptotic properties. Both factors have been implicated in the regulation of the transition from the G1 phase to the S phase in the mammalian cell cycle. However, whether cell death triggered by these molecules is dependent on the cell's position in the ongoing cell cycle remained elusive. Using centrifugal elutriation we here show for the first time that c-Myc induces apoptosis in G1 and in G2 phase, whereas E2F-1-induced apoptosis specifically occurs in G1. S phase cells are resistant to cell death triggered by these factors. We demonstrate that this is not a general phenomenon, since S phase cells are susceptible to apoptosis induced by treatment with actinomycin D and to the anti-apoptotic activity of Bcl-2. Our data indicate that S phase cells harbour specific protective activities against c-Myc- and E2F-1-induced apoptosis. Our results demonstrate that these transcription factors, although probably sharing specific apoptotic pathways, also take distinct routes to induce cell death and that apoptosis can occur at different phases of the cell cycle depending on the apoptotic stimulus. In this report we present the usefulness of a new approach to determine the regulation of apoptosis in the ongoing unperturbated cell cycle. This approach has clear implications for the identification of target genes involved in the regulation of cell death.
Asunto(s)
Apoptosis , Proteínas Portadoras , Proteínas de Ciclo Celular , Proteínas de Unión al ADN , Proteínas Proto-Oncogénicas c-myc/biosíntesis , Factores de Transcripción/biosíntesis , Animales , Ciclo Celular , Línea Celular , Factores de Transcripción E2F , Factor de Transcripción E2F1 , Regulación Neoplásica de la Expresión Génica , Proteínas Proto-Oncogénicas c-myc/genética , Ratas , Proteína 1 de Unión a Retinoblastoma , Factor de Transcripción DP1 , Factores de Transcripción/genéticaRESUMEN
In the mammalian cell cycle, the transition from the G1 phase to S phase, in which DNA replication occurs, is dependent on tight cell size control and has been shown to be regulated by the cyclin-dependent kinases (Cdks) 2, 3, 4 and 6. Activities of Cdks are controlled by association with cyclins and reversible phosphorylation reactions. An additional level of regulation is provided by inhibitors of Cdks. G1-S and S phase substrates of these enzymes include proteins implicated in replication and transcription. Whereas the regulation and role of Cdk2, 4 and 6 has intensively been studied, less is known about Cdk3. Recent data provide first insights into the regulation of Cdk3-associate kinase activity and suggest a model how Cdk3 participates in the regulation of the G1-S transition. Although it has been shown that these G1-Cdks are absolutely essential for a proper transition into S phase, their physiological activation is not sufficient to directly initiate replication independently of cell size. Evidence obtained from yeast and Xenopus indicate the initiation of DNA replication to be a two-step process: the origin recognition complex, Cdc6 and Mcm proteins are required for establishing the prereplicative complex and the activities of Cdks and of Cdc7 kinase then trigger the G1-S transition. Recent findings provide evidence that the overall mechanism of initiation of replication is conserved in mammalian cells.
Asunto(s)
Proteínas Portadoras , Proteínas de Ciclo Celular , Ciclo Celular , Quinasas Ciclina-Dependientes/metabolismo , Proteínas de Unión al ADN , Animales , Quinasas Ciclina-Dependientes/antagonistas & inhibidores , Replicación del ADN , Factores de Transcripción E2F , Fase G1 , Proteína 1 de Unión a Retinoblastoma , Fase S , Factores de Transcripción/fisiologíaRESUMEN
LR7/8B is a member of the low density lipoprotein receptor gene family that is specifically synthesized in the brain. Here we have functionally expressed in 293 cells the splice variant harboring eight ligand binding repeats (LR8B). As assessed by confocal microscopy, the expressed receptor is localized to the plasma membrane. Importantly, in cell binding experiments, we demonstrate that this protein is a receptor for activated alpha2-macroglobulin. Because to date low density lipoprotein receptor-related protein (LRP) has been shown to be the only alpha2-macroglobulin receptor in brain, we became interested in the expression pattern of both proteins at the cellular level in the brain. LR7/8B is expressed in large neurons and Purkinje cells of the cerebellum and in cells constituting brain barrier systems such as the epithelial cells of the choroid plexus, the arachnoidea, and the endothelium of penetrating blood vessels. Anti-LR7/8B antibody stains the plasma membrane, dendrites, and vesicular structures close to the cell membrane of neurons, especially of Purkinje cells. In contrast, LRP is present in patchy regions around large neurons and most prominently in the glomeruli of the stratum granulare of the cerebellum. This suggests that, contrary to LR7/8B, LRP is expressed in synaptic regions of the neurons; furthermore, there is a striking difference in the expression patterns of LR7/8B and LRP in the choroid plexus. Whereas LRP shows baso-lateral and apical localization in the epithelial cells, LR7/8B is restricted to the apical cell aspect facing the cerebrospinal fluid. Finally, these studies were extended to cultured primary rat neurons, where double immunofluorescence labeling with anti-LR7/8B and anti-microtubuli-associated protein 2 (MAP2) confirmed the somatodendritic expression of the receptor. Based upon these data, we propose that LR7/8B is involved in the clearance of alpha2-macroglobulin.proteinase complexes and/or of other substrates bound to alpha2-macroglobulin from the cerebrospinal fluid and from the surface of neurons.
Asunto(s)
Empalme Alternativo , Encéfalo/metabolismo , Familia de Multigenes , Receptores Inmunológicos/genética , Receptores de LDL/genética , Animales , Sitios de Unión , Línea Celular , Pollos , Variación Genética , Humanos , Inmunohistoquímica , Cinética , Proteína 1 Relacionada con Receptor de Lipoproteína de Baja Densidad , Ratas , Receptores Inmunológicos/análisis , Receptores Inmunológicos/metabolismo , Receptores de LDL/análisis , Receptores de LDL/metabolismo , Proteínas Recombinantes/metabolismo , Secuencias Repetitivas de Aminoácido , Transfección , alfa-Macroglobulinas/metabolismoRESUMEN
Although a remarkable number of genes has been identified that are either activated or repressed via c-Myc, only few of them obviously contribute to Myc's biological effect--the induction of proliferation. We found that in logarithmically growing cells overexpression of Myc specifically induces thymidine kinase (TK) mRNA expression and enzyme activity, whereas loss of one allele of Myc causes downregulation of this enzyme. We show that activation of Myc triggers high levels of this normally strictly S-phase-regulated DNA metabolism enzyme in serum arrested G0 cells and causes high and constant levels of TK expression throughout the entire ongoing cell cycle. Induction of TK by Myc requires an intact transcriptional activation domain. Myc-induced deregulation of this enzyme is paralleled by alterations of protein binding at the E2F-site of the TK promoter. We further show that cell growth arrest by the cyclin-dependent kinase inhibitor p16 is abrogated by overexpression of Myc and that co-overexpression of p16 cannot inhibit the Myc-induced up-regulation of TK expression. Our data demonstrate TK to be a cellular target of Myc independently of the status of cell proliferation and provide evidence that the transcription factor E2F might be involved in this process.
Asunto(s)
Proteínas de Ciclo Celular , Proteínas de Unión al ADN , Proteínas Proto-Oncogénicas c-myc/fisiología , Timidina Quinasa/metabolismo , Animales , Proteínas Portadoras/genética , División Celular/genética , Línea Celular , Inhibidor p16 de la Quinasa Dependiente de Ciclina , Factores de Transcripción E2F , Activación Enzimática/fisiología , Regiones Promotoras Genéticas , ARN Mensajero/genética , Ratas , Proteína 1 de Unión a Retinoblastoma , Timidina Quinasa/genética , Factor de Transcripción DP1 , Factores de Transcripción/metabolismo , Regulación hacia ArribaRESUMEN
The transcription factor E2F activates genes required for S phase, such as cyclin E and cyclin A. We show that, contrary to long term effects of E2F-1 overexpression, short ectopic overexpression of this transcription factor in logarithmically growing cells does neither affect the cell cycle distribution nor the cell size, but heavily induces cyclin E and A expression as well as cyclin E- and A-dependent kinase activities. We further separated logarithmically growing E2F-1-overexpressing cells according to their different cell cycle phases by centrifugal elutriation. These experiments revealed that deregulated E2F-1 expression triggers high levels of cyclin E and A expression and kinase activities in small early G1 cells, normally not exhibiting these activities. These effects on the regulation of cyclin E- and A-associated kinases are not accompanied by any detectable alteration in the rate of progression through the cell cycle, suggesting that these changes are independent of any mitogenic properties of E2F-1.
Asunto(s)
Proteínas Portadoras , Proteínas de Ciclo Celular , Ciclo Celular , Quinasas Ciclina-Dependientes/metabolismo , Ciclinas/genética , Proteínas de Unión al ADN , Factores de Transcripción/genética , Animales , Línea Celular , Factores de Transcripción E2F , Factor de Transcripción E2F1 , Regulación de la Expresión Génica , ARN Mensajero/genética , Ratas , Proteína 1 de Unión a Retinoblastoma , Factor de Transcripción DP1RESUMEN
We analysed cyclin D1 mRNA and protein expression in several different cell types after separating these cells according to their different cell cycle phases by centrifugal elutriation. In normal human and rat fibroblasts cyclin D1 expression is high in early to mid G1 and decreases about 6-7 fold before onset of replication. It has been demonstrated that specific transforming events, such as loss of functional retinoblastoma protein, overexpression of c-myc, and transfection with the human papillomavirus oncoproteins E6 and E7 cause transcriptional downregulation of cyclin D1 expression in logarithmically growing cells. We found that such transformed cells exhibit loss of the cell cycle-dependent cyclin D1 fluctuation accompanied with reduced upregulation of cyclin D1 in G1 phase. The data presented here provide the experimental support for a recently suggested model involving the function of the retinoblastoma protein in cyclin D1 cell cycle regulation.
Asunto(s)
Ciclo Celular , Transformación Celular Neoplásica , Transformación Celular Viral , Ciclinas/metabolismo , Proteínas Oncogénicas/metabolismo , Animales , Línea Celular Transformada , Células Cultivadas , Ciclina D1 , Ciclinas/genética , Fibroblastos , Regulación de la Expresión Génica , Humanos , Interfase , Mitosis , Proteínas Oncogénicas/genética , ARN Mensajero/metabolismo , Ratas , Fase S , Timidina Quinasa/metabolismo , Células Tumorales CultivadasRESUMEN
The role of alterations of the MTS1 tumor suppressor gene on chromosome 9p21, which encodes p16, the inhibitor of cyclin-dependent-kinase-4 and 6, in tumorigenesis is not yet clear. Phosphorylation of the retinoblastoma protein by cyclin-dependent kinases 4 and 6 prevents its interaction with the transcription factor E2F, which subsequently promotes the expression of S phase regulated genes, such as thymidine kinase. Although a role of p16 in this regulation has been presumed, there is no proof so far that loss of this tumor suppressor gene really affects E2F-mediated regulations. We investigated the regulation of thymidine kinase in phytohemagglutinin-stimulated normal human lymphocytes and in the p16-negative human acute lymphoblastic leukemia cell lines, MOLT-4 and CEM. Compared to normal lymphocytes, MOLT-4 and CEM cells exhibited an altered cell cycle regulation of thymidine kinase, a much higher intracellular activity of this enzyme, and higher thymidine kinase mRNA expression. Transient expression of p16 in normal human lymphocytes caused arrest in G1, but was without effect on the cell growth of MOLT-4 and CEM cells, although all of them express functional retinoblastoma protein. Nevertheless, in the two leukemia cell lines transient overexpression of p16 reestablished the normal regulation of thymidine kinase, paralleled by an increase of the underphosphorylated form of retinoblastoma protein and decrease of free E2F bound to its motif in the thymidine kinase promoter. We demonstrate that loss of p16 causes upregulation of this DNA precursor pathway enzyme via activation of E2F by a mechanism involving retinoblastoma protein.
Asunto(s)
Proteínas Portadoras/fisiología , Proteínas de Ciclo Celular , Proteínas de Unión al ADN , Regulación Enzimológica de la Expresión Génica , Regulación Neoplásica de la Expresión Génica , Timidina Quinasa/biosíntesis , Factores de Transcripción/fisiología , Ciclo Celular/genética , División Celular/genética , Células Cultivadas , Inhibidor p16 de la Quinasa Dependiente de Ciclina , Desoxicitidina Quinasa/biosíntesis , Regulación hacia Abajo , Factores de Transcripción E2F , Fase G1 , Células HeLa , Humanos , Linfocitos/citología , Linfocitos/efectos de los fármacos , Linfocitos/metabolismo , Fosforilación , Fitohemaglutininas/metabolismo , Fitohemaglutininas/farmacología , Leucemia-Linfoma Linfoblástico de Células Precursoras/genética , Leucemia-Linfoma Linfoblástico de Células Precursoras/patología , Proteína de Retinoblastoma/genética , Proteína de Retinoblastoma/metabolismo , Proteína de Retinoblastoma/fisiología , Proteína 1 de Unión a Retinoblastoma , Timidina Quinasa/genética , Factor de Transcripción DP1 , Factores de Transcripción/genética , Transcripción Genética , Transfección , Células Tumorales Cultivadas , Regulación hacia ArribaRESUMEN
Homozygous deletions of the tumor suppressor gene p16/MTS1 were reported in a wide variety of tumors and tumor cell lines. Its product inhibits the phosphorylation of the retinoblastoma protein (pRb) by CDK4 and CDK6. Because phosphorylation of pRb is a major regulatory event in the activation of the transcription factor E2F, a role for p16 in the regulation of E2F-dependent transcription was presumed. We investigated the effect of the loss of p16 on E2F-mediated transcription in a tumor progression model consisting of three cell lines originating from a common precursor cell--one p16-positive cell line established from the primary biopsy and two lines derived from more advanced stages of the tumor representing the same cell clone after loss of p16. We observed up- and deregulation of E2F-dependent transcription during the cell cycle of the p16-negative cell clones, which returned to normal after transient expression of p16. This p16-dependent regulation affects a set of enzymes necessary for the activation of all four DNA precursors; it is paralleled by the interconversion of transcriptionally active free E2F and transcriptionally inactive higher molecular complexes of E2F and is dependent on the existence of endogenous pRb. Furthermore, we show that p16-negative cell clones exhibit a growth advantage compared to their p16-positive counterparts. One might speculate that one feature of tumor progression could be deregulation of E2F-dependent transcription caused by loss of p16.
Asunto(s)
Proteínas Portadoras/genética , Proteínas de Ciclo Celular , Proteínas de Unión al ADN , ADN/metabolismo , Enzimas/genética , Factores de Transcripción/metabolismo , Proteínas Portadoras/metabolismo , Ciclo Celular , Inhibidor p16 de la Quinasa Dependiente de Ciclina , Factores de Transcripción E2F , Activación Enzimática , Enzimas/metabolismo , Eliminación de Gen , Regulación Enzimológica de la Expresión Génica , Regulación Neoplásica de la Expresión Génica , Genes Supresores de Tumor/genética , Células HeLa , Humanos , Proteína 1 de Unión a Retinoblastoma , Factor de Transcripción DP1RESUMEN
Rapidly growing oocytes in the laying hen are, in addition to the liver, targets of the so-called "reverse cholesterol transport" (RCT) (Vieira, P.M., Vieira, A.V., Sanders, E.J., Steyrer, E., Nimpf, J., and Schneider, W.J. (1995) J. Lipid Res. 36, 601-610), pointing to the importance of this process in nonplacental reproduction. We have begun to delineate the details of this unique transport pathway branch by molecular characterization of the first nonmammalian lecithin-cholesterol acyltransferase (LCAT), the enzyme that catalyzes an early step in RCT. The biological significance of the enzyme is underscored by the high degree of protein sequence identity (73%) maintained from chicken to man. Interestingly, the conservation extends much less to the cysteine residues; in fact, two of the cysteines thought to be important in mammalian enzymes (residues 31 and 184 in man) are absent from the chicken enzyme, providing proof of their dispensability for enzymatic activity. Antibodies prepared against a chicken LCAT fusion protein cross-react with human LCAT and identify a 64-kDa protein present in enzymatically active fractions obtained by hydrophobic chromatography of chicken serum. The developmental and tissue distribution pattern of LCAT in females is striking; during embryogenesis and adolescence, LCAT expression is extremely high in liver but undetectable in brain. Upon onset of laying, however, brain LCAT mRNA increases suddenly and is maintained at levels 5 times higher than in liver, in stark contrast to most mammals. In adult roosters, the levels of LCAT transcripts in brain are lower than in liver. Together with the molecular characterization of chicken LCAT, these newly discovered developmental changes and gender differences in its expression establish the avian oocyte/liver system as a powerful model to delineate in vivo regulatory elements of RCT.
Asunto(s)
Oocitos/enzimología , Fosfatidilcolina-Esterol O-Aciltransferasa/biosíntesis , Fosfatidilcolina-Esterol O-Aciltransferasa/química , Secuencia de Aminoácidos , Animales , Anticuerpos , Secuencia de Bases , Sitios de Unión , Northern Blotting , Encéfalo/enzimología , Embrión de Pollo , Pollos , Reacciones Cruzadas , Femenino , Expresión Génica , Humanos , Hígado/enzimología , Masculino , Mamíferos , Datos de Secuencia Molecular , Especificidad de Órganos , Oviposición , Papio , Fosfatidilcolina-Esterol O-Aciltransferasa/inmunología , Ratas , Proteínas Recombinantes de Fusión/inmunología , Homología de Secuencia de Aminoácido , PorcinosRESUMEN
It has been demonstrated that protein expression of p16, the inhibitor of cyclin-dependent kinase 4 and 6, increases 4 fold at the G1/S transition when serum-arrested cells are restimulated to logarithmic growth. We examined the cell cycle regulation of this cyclin-dependent kinase inhibitor in cells separated according to their cell cycle phases by centrifugal elutriation. Neither p16 mRNA nor its protein expression are regulated during the cell cycle of normal phytohemagglutinin-stimulated lymphocytes, retinoblastoma protein-negative cells, papilloma virus-transformed cells, and acute promyelocytic leukemia cells. p16 mRNA is constitutively expressed in cells in which we detected the normal E2F-dependent S-phase specific expression of thymidine kinase mRNA. We further observed a G1-phase specific expression of cyclin D1 mRNA in the same cells separated by centrifugal elutriation.
Asunto(s)
Proteínas Portadoras/biosíntesis , Ciclo Celular , Expresión Génica , Western Blotting , Proteínas Portadoras/análisis , División Celular , Ciclina D1 , Inhibidor p16 de la Quinasa Dependiente de Ciclina , Ciclinas/biosíntesis , Inhibidores Enzimáticos/análisis , Neoplasias del Ojo , Regulación Neoplásica de la Expresión Génica , Células HeLa , Humanos , Leucemia Promielocítica Aguda , Proteínas Oncogénicas/biosíntesis , Inhibidores de Proteínas Quinasas , ARN Mensajero/análisis , ARN Mensajero/biosíntesis , Retinoblastoma , Proteína de Retinoblastoma/análisis , Proteína de Retinoblastoma/biosíntesis , Timidina Quinasa/biosíntesis , Células Tumorales CultivadasRESUMEN
The binding and uptake of oxidatively modified low density lipoprotein (OxLDL) by mouse peritoneal macrophages occurs, in part, via the well characterized acetyl LDL receptor. However, several lines of evidence indicate that as much as 30-70% of the uptake can occur via a distinct receptor that recognizes OxLDL with a higher affinity than it recognizes acetyl LDL. We describe the partial purification and characterization of a 94- to 97-kDa plasma membrane protein from mouse peritoneal macrophages that specifically binds OxLDL. This receptor is shown to be distinct from the acetyl LDL receptor as well as from two other macrophage proteins that also bind OxLDL--the Fc gamma RII receptor and CD36. We suggest that this OxLDL-binding membrane protein participates in uptake of OxLDL by murine macrophages and also represents a receptor responsible for macrophage binding and phagocytosis of oxidatively damaged cells.
Asunto(s)
Moléculas de Adhesión Celular , Lipoproteínas LDL/metabolismo , Macrófagos/metabolismo , Receptores de Superficie Celular/aislamiento & purificación , Receptores de LDL/metabolismo , Animales , Antígenos CD/química , Antígenos CD36 , Femenino , Humanos , Técnicas In Vitro , Lipoproteínas LDL/química , Macrófagos/química , Proteínas de la Membrana/aislamiento & purificación , Proteínas de la Membrana/metabolismo , Ratones , Oxidación-Reducción , Conejos , Receptores de Superficie Celular/química , Receptores DepuradoresRESUMEN
Reduced hepatic membrane receptors for acetylated low-density lipoprotein (acetyl-LDL) and maleylated BSA (Mal-BSA) with apparent molecular masses of 35 kDa, 85 kDa and 15 kDa have been extracted from rat liver and separated by affinity chromatography as described by us previously [Ottnad, Via, Sinn, Freidrich, Ziegler & Dresel (1990) Biochem. J. 265, 689-698]. Binding of these three reduced scavenger receptors to oxidatively modified LDL has been now examined. Competition studies with receptor-phosphatidylcholine complexes and 131I-acetyl-LDL and 131I-Mal-BSA as ligands were conducted. Mal-BSA, acetyl-LDL and fully oxidized LDL were used as competitors, and differentiated in the three receptors three types of binding site: a class I binding site for acetyl-LDL, Mal-BSA and fully oxidized LDL; a class II binding site recognizing only 131I-Mal-BSA and class III binding sites recognizing 131I-Mal-BSA and fully oxidized LDL. The results of competition studies with mildly oxidized LDL and polyadenylic acid demonstrated that the binding sites might be even more heterogenous. Thus there is evidence that the reconstituted receptors either have several binding sites for each of the various ligands or are functionally different, despite the fact that they do not differ in their apparent molecular masses.
Asunto(s)
Lipoproteínas LDL/metabolismo , Hígado/metabolismo , Receptores de LDL/metabolismo , Albúmina Sérica Bovina , Albúminas/metabolismo , Animales , Sitios de Unión , Unión Competitiva , Membrana Celular/metabolismo , Humanos , Masculino , Peso Molecular , Oxidación-Reducción , Fosfatidilcolinas/metabolismo , Ratas , Receptores de LDL/química , Receptores de LDL/aislamiento & purificaciónRESUMEN
The binding characteristics of reduced hepatic membrane proteins for acetylated low-density lipoprotein (acetyl-LDL) and maleylated bovine serum albumin (Mal-BSA) have been examined. Two receptor activities were extracted from hepatic membranes in the presence of octyl beta-D-glucoside and beta-mercaptoethanol, and were separated by chromatography on Mal-BSA-Sepharose 4B. The receptors were revealed by ligand blotting. The active binding proteins had apparent molecular masses of 35 and 15 kDa in SDS/polyacrylamide gels. Equilibrium studies with protein-phosphatidylcholine complexes indicated that the reduced 35 kDa protein expresses two binding sites for Mal-BSA and one for acetyl-LDL, whereas the 15 kDa protein-phosphatidylcholine complex binds 131I-Mal-BSA and 131I-acetyl-LDL with a 4:1 stoichiometry. 131I-Mal-BSA binding was linear with both proteins, with a Kd of 4.8 nM at the 35 kDa protein and a Kd of 5.6 nM at the 15 kDa protein. The 35 kDa protein displayed saturable binding of 131I-acetyl-LDL with a Kd of 5 nM; the 15 kDa binding protein bound 131I-acetyl-LDL with a Kd of 2.3 nM. A 85 kDa protein was obtained by Mal-BSA-Sepharose chromatography when the hepatic membranes had been solubilized with Triton X-100 in presence of GSH/GSSG. This protein displayed saturable 131I-Mal-BSA binding with a Kd of 30 nM and 131I-acetyl-LDL binding with a Kd of 6.5 nM. The 131I-Mal-BSA binding capacity was four times higher than that of 131I-acetyl-LDL. Competition studies with the 35 kDa, 15 kDa and 85 kDa proteins binding Mal-BSA, acetyl-LDL, formylated albumin and polyanionic competitors provide evidence for the existence of more than one class of binding sites at the reduced binding proteins.
Asunto(s)
Lipoproteínas LDL/metabolismo , Hígado/metabolismo , Receptores de Superficie Celular/metabolismo , Receptores de LDL/metabolismo , Albúmina Sérica Bovina/metabolismo , Acetilación , Animales , Cromatografía de Afinidad , Cromatografía en Gel , Electroforesis en Gel de Poliacrilamida , Humanos , Ligandos , Proteínas de la Membrana/metabolismo , Ratas , Receptores de AlbúminaRESUMEN
Membranes from rat liver were analysed under reducing conditions. The components of the soluble membranes responsible for the binding of acetylated low density lipoprotein (acetyl-LDL) and maleylated bovine serum albumin (Mal-BSA) were chromatographed on a polyethyleneimine-cellulose column and subsequently separated by gel electrophoresis. For both ligands a major binding protein (Mr = 35,000) was revealed by ligand blotting. A minor protein (Mr greater than 67,000) exhibited little binding. The Scatchard plot of the 131I-Mal-BSA binding data of the 35 kDa protein was linear, with a Kd of 17.3 nM. High concentrations of acetyl-LDL competed for half of the 131I-Mal-BSA binding. Excessive Mal-BSA competed for all the visible acetyl-LDL binding. The findings indicate the existence, in the reduced hepatic membrane, of a 35 kDa protein that has two binding sites for 131I-Mal-BSA and one binding site for acetyl-LDL.