RESUMO
V gene assembly, class switch recombination, and somatic hypermutation are gene-modifying processes essential to the development of an effective Ab response. If inappropriately applied, however, these processes can mediate genetic changes that lead to disease (e.g., lymphoma). A series of control elements within the Ig H chain (Igh) locus has been implicated in regulating these processes as well as in regulating IgH gene transcription. These include the intronic enhancer (Emu) and several elements at the 3' end of the locus (hs1,2, hs3a, hs3b, and hs4) known collectively as the 3' regulatory region. Although it is clear that the Emu plays a unique role in V gene assembly, it has not been established whether there are unique functions for each element within the 3' regulatory region. In earlier studies in mice and in mouse cell lines, pairwise deletion of hs3b and hs4 had a dramatic effect on both class switch recombination and IgH gene transcription; deletion of an element almost identical with hs3b (hs3a), however, yielded no discernible phenotype. To test the resulting hypothesis that hs4 is uniquely required for these processes, we induced the deletion of hs4 within a bacterial artificial chromosome transgene designed to closely approximate the 3' end of the natural Igh locus. When introduced into an Ig-secreting cell line, an Igalpha transcription unit within the bacterial artificial chromosome was expressed efficiently and the subsequent deletion of hs4 only moderately affected Igalpha expression. Thus, hs4 does not play a uniquely essential role in the transcription of a productively rearranged Ig VDJCalpha transcription unit.
Assuntos
Região 3'-Flanqueadora/genética , Elementos Facilitadores Genéticos , Rearranjo Gênico de Cadeia Pesada de Linfócito B , Imunoglobulina A/genética , Regiões Constantes de Imunoglobulina/genética , Cadeias alfa de Imunoglobulina/genética , Sequências Reguladoras de Ácido Nucleico , Transcrição Gênica , Animais , Linhagem Celular Tumoral , Imunoglobulina A/biossíntese , Regiões Constantes de Imunoglobulina/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , CamundongosRESUMO
OBJECTIVE: To examine the difference in expression of messenger RNA (mRNA) transcripts for polymeric immunoglobulin receptor (plgR), alpha-chain, and J-chain determined by use of quantitative real-time reverse transcription-polymerase chain reaction (QRT-PCR) assays in duodenal biopsy specimens obtained from dogs with and without chronic diarrhea. SAMPLE POPULATION: Biopsy specimens of the proximal portion of the duodenum were obtained endoscopically from 39 dogs evaluated because of chronic diarrhea (12 German Shepherd Dogs and 27 non-German Shepherd Dog breeds); specimens were also obtained from a control group of 7 dogs evaluated because of other gastrointestinal tract diseases and 2 dogs that were euthanatized as a result of nongastrointestinal tract disease. PROCEDURE: Dogs were anesthetized, and multiple mucosal biopsy specimens were obtained endoscopically at the level of the caudal duodenal flexure by use of biopsy forceps; in 2 control dogs, samples were obtained from the descending duodenum within 5 minutes of euthanasia. One-step QRT-PCR was used to quantify the level of expression of transcripts for the housekeeper gene glyceraldehyde-3-phosphate dehydrogenase, plgR, alpha-chain, and J-chain in duodenal mucosal tissue. RESULTS: There was no significant difference in the level of expression of any transcript among non-German Shepherd Dog breeds without diarrhea (control group), non-German Shepherd Dog breeds with chronic diarrhea, and German Shepherd Dogs with chronic diarrhea. Conclusions and Clinical Relevance-Results indicated that the susceptibility of German Shepherd Dogs to chronic diarrhea is not a result of simple failure of transcription of the key genes that encode molecules involved in mucosal IgA secretion.
Assuntos
Diarreia/veterinária , Doenças do Cão/imunologia , Imunoglobulina A Secretora/biossíntese , Cadeias J de Imunoglobulina/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Receptores de Imunoglobulina Polimérica/biossíntese , Animais , Doença Crônica , Diarreia/imunologia , Cães , Duodeno/imunologia , Feminino , Expressão Gênica , Imunoglobulina A Secretora/genética , Cadeias J de Imunoglobulina/genética , Cadeias alfa de Imunoglobulina/genética , Mucosa Intestinal/imunologia , Masculino , RNA Mensageiro/análise , Receptores de Imunoglobulina Polimérica/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa/veterináriaRESUMO
By substituting the H chain C region of IgM with that of IgG, IgA, or IgE, class switching enables Abs to acquire new effector functions that are crucial for the neutralization of invading pathogens. Class switching occurs through class switch DNA recombination (CSR) and usually requires engagement of CD40 on B cells by CD40 ligand on Ag-activated CD4(+) T cells. CSR must be tightly regulated because abnormal IgG and IgA production favors the onset of autoimmunity, whereas increased switching to IgE leads to atopy. These inflammatory disorders can be triggered or exacerbated by EBV infection. In this study, we show that EBV induces CD40-independent CSR from C( micro ) to multiple downstream C(gamma), C(alpha), and C(epsilon) genes through latent membrane protein 1 (LMP1), a CD40-like viral protein that signals in a ligand-independent fashion. LMP1-induced CSR is associated with transcriptional activation of germline C(gamma), C(alpha), and C(epsilon) genes and triggers the up-regulation of activation-induced cytidine deaminase, a crucial component of the CSR machinery. In addition, LMP1 induces B cells to express B cell-activating factor of the TNF family and a proliferation-inducing ligand, two molecules that mediate B cell survival and T cell-independent Ab production. B cell-activating factor of the TNF family and a proliferation-inducing ligand cooperate with LMP1 to induce Ig class switching because their neutralization by appropriate soluble decoy receptors attenuates CSR in LMP1-expressing B cells. By showing that LMP1 triggers T cell-independent CSR, our findings suggest that EBV could play an important role in the pathogenesis of disorders with aberrant IgG, IgA, and/or IgE production.
Assuntos
Herpesvirus Humano 4/imunologia , Switching de Imunoglobulina , Cadeias Pesadas de Imunoglobulinas/biossíntese , Proteínas de Membrana/fisiologia , Neuropeptídeos/fisiologia , Subpopulações de Linfócitos T/imunologia , Fator de Necrose Tumoral alfa/fisiologia , Proteínas da Matriz Viral/fisiologia , Adjuvantes Imunológicos/biossíntese , Adjuvantes Imunológicos/fisiologia , Fator Ativador de Células B , Subpopulações de Linfócitos B/enzimologia , Subpopulações de Linfócitos B/imunologia , Subpopulações de Linfócitos B/metabolismo , Sequência de Bases , Células Cultivadas , Citidina Desaminase/biossíntese , Regulação da Expressão Gênica/imunologia , Células HL-60 , Herpesvirus Humano 4/genética , Humanos , Switching de Imunoglobulina/genética , Cadeias Pesadas de Imunoglobulinas/genética , Cadeias alfa de Imunoglobulina/biossíntese , Cadeias alfa de Imunoglobulina/genética , Cadeias épsilon de Imunoglobulina/biossíntese , Cadeias épsilon de Imunoglobulina/genética , Cadeias mu de Imunoglobulina/biossíntese , Cadeias mu de Imunoglobulina/genética , Ativação Linfocitária , Proteínas de Membrana/biossíntese , Proteínas de Membrana/genética , Dados de Sequência Molecular , NF-kappa B/fisiologia , Neuropeptídeos/biossíntese , Proteínas Nucleares , Regiões Promotoras Genéticas/imunologia , Recombinação Genética , Transcrição Gênica/imunologia , Membro 13 da Superfamília de Ligantes de Fatores de Necrose Tumoral , Fator de Necrose Tumoral alfa/biossíntese , Fator de Necrose Tumoral alfa/genética , Regulação para Cima/genética , Regulação para Cima/imunologia , Proteínas da Matriz Viral/genéticaRESUMO
CD153 (CD30 ligand) is a member of the TNF ligand/cytokine family expressed on the surface of human B cells. Upon exposure to IL-4, a critical Ig class switch-inducing cytokine, Ag-activated T cells express CD30, the CD153 receptor. The observation that dysregulated IgG, IgA, and/or IgE production is often associated with up-regulation of T cell CD30 prompted us to test the hypothesis that engagement of B cell CD153 by T cell CD30 modulates Ig class switching. In this study, we show that IgD+ IgM+ B cells up-regulate CD153 in the presence of CD154 (CD40 ligand), IL-4, and B cell Ag receptor engagement. In these cells, CD153 engagement by an agonistic anti-CD153 mAb or T cell CD30 inhibits S mu-->Sgamma, Smu-->Salpha, and S mu-->Sepsilon class switch DNA recombination (CSR). This inhibition is associated with decreased TNFR-associated factor-2 binding to CD40, decreased NF-kappaB binding to the CD40-responsive element of the Cgamma3 promoter, decreased Igamma3-Cgamma3 germline gene transcription, and decreased expression of Ku70, Ku80, DNA protein kinase, switch-associated protein-70, and Msh2 CSR-associated transcripts. In addition, CD153 engagement inhibits IgG, IgA, and IgE production, and this effect is associated with reduced levels of B lymphocyte maturation protein-1 transcripts, and increased binding of B cell-specific activation protein to the Ig 3' enhancer. These findings suggest that CD30+ T cells modulate CSR as well as IgG, IgA, and IgE production by inducing reverse signaling through B cell CD153.
Assuntos
Subpopulações de Linfócitos B/imunologia , Switching de Imunoglobulina/imunologia , Imunoglobulina D/biossíntese , Imunoglobulina M/biossíntese , Antígeno Ki-1/biossíntese , Glicoproteínas de Membrana/imunologia , Recombinação Genética/imunologia , Proteínas Repressoras , Subpopulações de Linfócitos T/imunologia , Subpopulações de Linfócitos B/metabolismo , Ligação Competitiva/imunologia , Antígenos CD28/imunologia , Antígenos CD28/metabolismo , Ligante CD30 , Antígenos CD40/imunologia , Antígenos CD40/metabolismo , Ligante de CD40 , Diferenciação Celular/imunologia , Linhagem Celular , Células Cultivadas , Citocinas/fisiologia , Proteínas de Ligação a DNA/metabolismo , Centro Germinativo/citologia , Centro Germinativo/imunologia , Centro Germinativo/metabolismo , Humanos , Tolerância Imunológica/genética , Regiões Constantes de Imunoglobulina/biossíntese , Regiões Constantes de Imunoglobulina/genética , Imunoglobulina G/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Cadeias alfa de Imunoglobulina/genética , Cadeias épsilon de Imunoglobulina/biossíntese , Cadeias épsilon de Imunoglobulina/genética , Cadeias gama de Imunoglobulina/biossíntese , Cadeias gama de Imunoglobulina/genética , Cadeias mu de Imunoglobulina/biossíntese , Cadeias mu de Imunoglobulina/genética , Imunofenotipagem , Interleucina-4/antagonistas & inibidores , Interleucina-4/fisiologia , Antígeno Ki-1/metabolismo , Ligantes , Glicoproteínas de Membrana/antagonistas & inibidores , Glicoproteínas de Membrana/biossíntese , Glicoproteínas de Membrana/metabolismo , Glicoproteínas de Membrana/fisiologia , Proteínas Nucleares/metabolismo , Fator de Transcrição PAX5 , Tonsila Palatina/citologia , Tonsila Palatina/imunologia , Tonsila Palatina/metabolismo , Plasmócitos/imunologia , Fator 1 de Ligação ao Domínio I Regulador Positivo , Regiões Promotoras Genéticas/imunologia , Ligação Proteica/imunologia , Proteínas/metabolismo , Receptores de Antígenos de Linfócitos T/imunologia , Receptores de Antígenos de Linfócitos T/metabolismoRESUMO
The maturation of IgM-expressing B cells to IgM-secreting plasma cells is associated with both an increase in mu mRNA and the ratio of secreted to membrane forms of mu mRNA which differ at the 3' termini. In contrast, both in vitro and in vivo the secreted form of alpha mRNA is predominant at all stages in the development of a secretory IgA response. Previous studies demonstrated that preferential usage of the alpha s poly(A) site does not result from transcription termination and is independent of either the poly(A) sites or the 3' splice site associated with the exon encoding the membrane exon of IgA (alpha M). The present study demonstrates that a 349-bp region located 774 bp 3' to the alpha s poly(A) site is required for the preferential usage of the alpha s terminus. This region, which is the first isotype-specific cis-acting regulatory sequence not immediately adjacent to a secretory poly(A) site to be identified, contains regulatory elements that increase the efficiency of polyadenylation/cleavage. A ubiquitous, approximately 58-kDa RNA-binding protein interacts specifically with this regulatory region. These studies support the premise that cis-acting elements unique to each CH gene can impinge upon a common mechanism regulating Ig mRNA processing.
Assuntos
Regiões Constantes de Imunoglobulina/genética , Cadeias alfa de Imunoglobulina/genética , Íntrons/genética , Processamento Pós-Transcricional do RNA/imunologia , RNA Mensageiro/metabolismo , Receptores de Antígenos de Linfócitos B/genética , Sequência de Bases , Linfoma de Burkitt , Rearranjo Gênico de Cadeia Pesada de Linfócito B , Humanos , Regiões Constantes de Imunoglobulina/biossíntese , Regiões Constantes de Imunoglobulina/metabolismo , Cadeias alfa de Imunoglobulina/biossíntese , Cadeias alfa de Imunoglobulina/metabolismo , Peso Molecular , Poli A/genética , Poli A/metabolismo , Precursores de RNA/metabolismo , Processamento Pós-Transcricional do RNA/genética , Receptores de Antígenos de Linfócitos B/metabolismo , Transdução de Sinais/genética , Transdução de Sinais/imunologia , Células Tumorais CultivadasRESUMO
Ten lines of transgenic mice secreting transmissible gastroenteritis coronavirus (TGEV) neutralizing recombinant monoclonal antibodies (rMAbs) into the milk were generated. The rMAb light- and heavy-chain genes were assembled by fusing the genes encoding the variable modules of the murine MAb 6A.C3, which binds an interspecies conserved coronavirus epitope essential for virus infectivity, and a constant module from a porcine myeloma with the immunoglobulin A (IgA) isotype. The chimeric antibody led to dimer formation in the presence of J chain. The neutralization specific activity of the recombinant antibody produced in transiently or stably transformed cells was 50-fold higher than that of a monomeric rMAb with the IgG1 isotype and an identical binding site. This rMAb had titers of up to 10(4) by radioimmunoassay (RIA) and neutralized virus infectivity up to 10(4)-fold. Of 23 transgenic mice, 17 integrated both light and heavy chains, and at least 10 of them transmitted both genes to the progeny, leading to 100% of animals secreting functional TGEV neutralizing antibody during lactation. Selected mice produced milk with TGEV-specific antibody titers higher than 10(6) as determined by RIA, neutralized virus infectivity by 10(6)-fold, and produced up to 6 mg of antibody per ml. Antibody expression levels were transgene copy number independent and integration site dependent. Comicroinjection of the genomic beta-lactoglobulin gene with rMAb light- and heavy-chain genes led to the generation of transgenic mice carrying the three transgenes. The highest antibody titers were produced by transgenic mice that had integrated the antibody and beta-lactoglobulin genes, although the number of transgenic animals generated does not allow a definitive conclusion on the enhancing effect of beta-lactoglobulin cointegration. This approach may lead to the generation of transgenic animals providing lactogenic immunity to their progeny against enteric pathogens.
Assuntos
Anticorpos Antivirais/biossíntese , Imunoglobulina A/biossíntese , Camundongos Transgênicos , Leite/imunologia , Vírus da Gastroenterite Transmissível/imunologia , Sequência de Aminoácidos , Animais , Anticorpos Monoclonais/biossíntese , Anticorpos Antivirais/genética , Anticorpos Antivirais/imunologia , Sequência de Bases , Células COS , Linhagem Celular , Linhagem Celular Transformada , DNA Complementar , Humanos , Imunoglobulina A/genética , Isotipos de Imunoglobulinas , Cadeias alfa de Imunoglobulina/biossíntese , Cadeias alfa de Imunoglobulina/genética , Cadeias kappa de Imunoglobulina/biossíntese , Cadeias kappa de Imunoglobulina/genética , Camundongos , Dados de Sequência Molecular , Testes de Neutralização , Proteínas Recombinantes/biossíntese , Suínos , Células Tumorais CultivadasRESUMO
The Ig heavy chain locus contains a number of binding sites for the transcriptional activator, c-Rel. In this study, we evaluated the capacity of B cells from mice made genetically deficient in the C-terminal, transactivation domain of the c-Rel protein (delta c-Rel) to undergo Ig class switching. Flow-cytometric and digestion circularization PCR analyses revealed that delta c-Rel B cells failed to switch to IgG3 in response to LPS alone, or to IgG1 or IgE in response to LPS + IL-4. This failure to switch to IgG3 or IgG1 was associated with a corresponding loss of germline CH gamma 3 or CH gamma 1 RNA. However, the defective switching to IgE in delta c-Rel B cells was associated with normal levels of germline CH epsilon RNA relative to control B cells. The ability of delta c-Rel B cells to switch to IgG1, in response to LPS + IL-4, could be restored through the action(s) of additional stimuli, and this was associated with induction of normal levels of germline CH gamma 1 RNA relative to controls. In contrast, LPS-activated B cells from delta c-Rel mice underwent normal switching to IgA in the presence of TGF-beta, relative to control B cells. This was associated with equivalent steady state levels of germline CH alpha RNA between the two B cell populations. These data are the first to demonstrate a key and selective role for c-Rel in the regulation of Ig class switching. Furthermore, distinct differences are revealed in the Ig isotype induction profiles of B cells lacking c-Rel activity vs those deficient in p50/nuclear factor-kappa B.
Assuntos
Linfócitos B/metabolismo , Switching de Imunoglobulina , Regiões Constantes de Imunoglobulina/genética , Cadeias Pesadas de Imunoglobulinas/genética , Proteínas Proto-Oncogênicas/deficiência , Proteínas Proto-Oncogênicas/genética , Transcrição Gênica/imunologia , Ativação Transcricional/imunologia , Animais , Linfócitos B/imunologia , Células Germinativas/imunologia , Imunoglobulina A/biossíntese , Imunoglobulina E/biossíntese , Imunoglobulina G/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Cadeias épsilon de Imunoglobulina/biossíntese , Cadeias épsilon de Imunoglobulina/genética , Cadeias gama de Imunoglobulina/biossíntese , Cadeias gama de Imunoglobulina/genética , Lipopolissacarídeos/farmacologia , Ativação Linfocitária/genética , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Mutantes , Estrutura Terciária de Proteína , Proteínas Proto-Oncogênicas/fisiologia , Proteínas Proto-Oncogênicas c-rel , RNA/biossínteseRESUMO
Inasmuch as transcription of unrearranged, or germ-line, Ig CH genes appears to direct switch recombination, understanding the regulation of this transcription is essential for understanding the regulation of class switching. Transforming growth factor-beta 1 (TGF-beta 1) induces germ-line alpha transcripts and increases class switching to IgA in the I.29 mu B lymphoma and in Peyer's patch and splenic B cells. It has been previously demonstrated that induction of germ-line alpha transcripts by TGF-beta occurs at the transcriptional level in I.29 mu cells. We now demonstrate that the DNA segment located 5' to the initiation sites of germ-line alpha RNA drives expression of a luciferase reporter gene construct in transient transfection experiments. Full constitutive expression requires no more than 106 bp of the 5' flanking segment. By creating a series of deletion and substitution mutations, we have demonstrated that an ATF/CRE site residing within this region is very important for constitutive expression of the germ-line alpha promoter, but mutation of this motif does not diminish TGF-beta induction. Inducibility by TGF-beta requires additional sequences residing between -128 to -106 relative to the first RNA initiation site. Two copies of a tandemly repeated sequence 5' CA-CAG(G)CCAGAC 3' (termed Ig alpha TGF-beta-RE) are located in the region from -127 to -105. An oligonucleotide containing multimers of these repeats confers TGF-beta inducibility to a heterologous promoter. An additional copy of the TGF-beta-RE was identified at -41/-30 and its deletion reduces the TGF-beta response. Thus, we conclude that tandem repeats of a novel TGF-beta-RE are the positive regulatory element for the TGF-beta response. Our study provides further evidence that TGF-beta directs class switching to IgA through induction of transcription of the germ-line C alpha gene and demonstrates that TGF-beta can activate the promoter for the germ-line alpha gene.
Assuntos
Proteínas Sanguíneas/fisiologia , Regulação da Expressão Gênica/fisiologia , Genes de Imunoglobulinas/fisiologia , Regiões Constantes de Imunoglobulina/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Proteínas de Neoplasias/fisiologia , Fatores de Transcrição/fisiologia , Transcrição Gênica/fisiologia , Fator de Crescimento Transformador beta/fisiologia , Fatores Ativadores da Transcrição , Animais , Sequência de Bases , Linhagem Celular , Imunoglobulina A/biossíntese , Camundongos , Dados de Sequência Molecular , Mutagênese Sítio-Dirigida , Sondas de Oligonucleotídeos , Regiões Promotoras Genéticas/fisiologia , Mapeamento por Restrição , Homologia de Sequência do Ácido Nucleico , TransfecçãoRESUMO
At the present, immunoproliferative small intestinal disease (IPSID) is considered a fairly homogeneous entity. Isolated heavy chain production is so closely related with IPSID that has been considered as a natural biologic marker for it. By contrast, we report here the case of a 63-year-old female that developed a multinodular small bowel lymphoma without clinical malabsorption symptoms. The main tumour mass was located in proximal jejunum and the neighbour intestinal mucosa did not show neoplastic cell infiltrates. Immunohistochemical methods demonstrated restrictive presence of IgA1 subclass in the neoplastic cells without presence of light chains. Cases as present are extremely infrequent and their potential relationship with IPSID has not been completely outlined, being useful in trying to understand the spectrum of gut lymphomas.
Assuntos
Cadeias Pesadas de Imunoglobulinas/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Neoplasias do Jejuno/metabolismo , Linfoma/metabolismo , Feminino , Humanos , Doença Imunoproliferativa do Intestino Delgado/metabolismo , Neoplasias do Jejuno/patologia , Linfoma/patologia , Pessoa de Meia-IdadeRESUMO
A human IgE-producing myeloma has been cultivated in vitro as a continuous cell line (U-266) since 1968. Analysis of immunoglobulin production during early passages of the cell line demonstrated a high synthesis rate of monoclonal IgE. Analysis of late passages, cultivated after 1980, revealed a 3-6-fold lower rate of IgE secretion. This decrease was accompanied by the appearance of small amounts of IgA in the culture medium together with IgE. RNA was extracted from a late passage of U-266 and analyzed by Northern blotting, using epsilon and alpha-specific oligonucleotides as hybridization probes. The results showed the presence of epsilon as well as alpha-specific mRNA. Moreover the results demonstrated that the latter mRNA was derived from the alpha 2 locus and that the epsilon and the alpha 2-specific mRNA contained the same V region sequences. Southern blot analysis of DNA from the late passage of the U-266 cell line failed to reveal a recombinatory switch from the epsilon locus to the alpha 2 locus. The expression of alpha 2 is thus likely to be caused by differential splicing rather than by an isotype switch at the DNA level.
Assuntos
Cadeias Pesadas de Imunoglobulinas/biossíntese , Isotipos de Imunoglobulinas/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Cadeias épsilon de Imunoglobulina/biossíntese , Mieloma Múltiplo/imunologia , Linhagem Celular , Humanos , Imunoensaio , Cadeias alfa de Imunoglobulina/genética , Mieloma Múltiplo/metabolismo , Hibridização de Ácido Nucleico , Fenótipo , RNA Neoplásico/análise , Células Tumorais CultivadasAssuntos
Neoplasias Intestinais , Intestino Delgado , Linfoma , Adolescente , Adulto , Doença Celíaca/complicações , Doença Celíaca/terapia , Criança , Feminino , Doença das Cadeias Pesadas/patologia , Doença das Cadeias Pesadas/terapia , Humanos , Cadeias alfa de Imunoglobulina/biossíntese , Neoplasias Intestinais/etiologia , Neoplasias Intestinais/patologia , Neoplasias Intestinais/terapia , Intestino Delgado/patologia , Linfoma/etiologia , Linfoma/patologia , Linfoma/terapia , Masculino , Pessoa de Meia-Idade , PrognósticoRESUMO
The regulation of the synthesis of membrane-bound and secreted IgA was investigated in the murine B lymphoma I.29 during the differentiation from IgA-bearing lymphocytes to IgA-secreting cells, as caused by treatment with lipopolysaccharide (LPS). LPS induced a threefold to fivefold increase in the amount of IgA synthesized, and induced a shift from the synthesis of the membrane form of alpha-chain (alpha m) to the synthesis of the secreted form of alpha-chain (alpha s), resulting in a 60-fold increase in the amount of IgA secreted. In vitro translation of sucrose gradient-fractionated RNA indicated that two mRNA molecules, 3.1 and 2.1 kilobase pairs (kb), encode alpha m-chains, whereas a smaller RNA molecule, 1.7 kb, encodes alpha s. Analyses by RNA blotting showed that the relative amounts of the three alpha mRNA changed rapidly during LPS-induced differentiation. The amount of the 3.1 and 2.1 kb alpha mRNA decreased, and the amount of the 1.7 kb alpha s mRNA increased in LPS-stimulated cells as compared with controls. These observations suggest that the regulation of alpha m/alpha s synthesis is controlled mostly at the pretranslational level.
Assuntos
Linfócitos B/metabolismo , Cadeias Pesadas de Imunoglobulinas/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Ativação Linfocitária , Linfoma/imunologia , Receptores de Antígenos de Linfócitos B/biossíntese , Animais , Linfócitos B/imunologia , Linhagem Celular , Transformação Celular Neoplásica/imunologia , Transformação Celular Neoplásica/metabolismo , Imunoglobulina A/biossíntese , Imunoglobulina A Secretora/biossíntese , Lipopolissacarídeos/farmacologia , Linfoma/metabolismo , Camundongos , RNA Mensageiro/análise , RNA Neoplásico/análiseAssuntos
Doença das Cadeias Pesadas/imunologia , Imunoglobulina A Secretora/biossíntese , Imunoglobulina A/biossíntese , Sequência de Aminoácidos , Linfócitos B/imunologia , Linfócitos B/patologia , Doença das Cadeias Pesadas/complicações , Doença das Cadeias Pesadas/patologia , Humanos , Regiões Constantes de Imunoglobulina/genética , Cadeias alfa de Imunoglobulina/biossíntese , Cadeias alfa de Imunoglobulina/genética , Intestino Delgado/patologia , Linfoma/complicações , Linfoma/imunologia , Conformação ProteicaRESUMO
A detailed study is described of a case of hairy cell leukaemia, presenting with a serum paraprotein of an immunoglobulin (Ig) class different from that synthesised by the neoplastic cells. The case was unusual in its association with leukaemic arthropathy but ultrastructurally the hairy cells were typical. By immunofluorenscence and immuno-electron microscopy the neoplastic cells expressed IgA lambda both on the cell surface and intracellularly in the rough endoplasmic reticulum, perinuclear space and Golgi apparatus. No Ig was observed in the ribosomal-lamellae complexes. These cells also synthesised and secreted Ig of class A lambda in culture. However the serum paraprotein was of class IgA chi and could not be attributed to an abnormal population of plasma cells in the bone marrow. There was no other evidence for myeloma and the IgA chi paraproteinaemia appeared to be benign, apparently unrelated to the neoplastic proliferation of hairy cells.
Assuntos
Leucemia de Células Pilosas/complicações , Paraproteinemias/complicações , Idoso , Transformação Celular Neoplásica/imunologia , Transformação Celular Neoplásica/ultraestrutura , Humanos , Cadeias alfa de Imunoglobulina/biossíntese , Cadeias gama de Imunoglobulina/biossíntese , Cadeias kappa de Imunoglobulina/biossíntese , Cadeias lambda de Imunoglobulina/biossíntese , Cadeias mu de Imunoglobulina/biossíntese , Leucemia de Células Pilosas/imunologia , Leucemia de Células Pilosas/ultraestrutura , Masculino , Paraproteinemias/sangue , Paraproteinemias/imunologia , Receptores FcRESUMO
We have compared the synthesis and processing of immunoglobulin alpha chains in two murine cell lines, a B cell lymphoma that expresses membrane-bound IgA and a hybridoma that secretes IgA. Results of biosynthetic labeling experiments demonstrated that membrane-bound and secreted alpha chains have two distinct intracellular precursors, of different molecular weights and isoelectric points. RNAs from both of these cell lines direct the synthesis in vitro of two alpha polypeptides of Mr 59,000 and 62,000, the larger one being the precursor for membrane-bound alpha chain and the smaller one being the precursor for secreted alpha chain. These cell lines each contain three RNAs, 1.7, 2.1, and 3.1 kilobases in length, which hybridize with cDNA for the alpha constant region and which are present in different concentrations. Our results suggest that the smallest RNA encodes the secreted alpha chain and one or both of the larger RNAs encode(s) the membrane-bound alpha chain.
Assuntos
Imunoglobulina A/genética , Cadeias Pesadas de Imunoglobulinas/genética , Cadeias alfa de Imunoglobulina/genética , Animais , Linfócitos B/imunologia , Linhagem Celular , Hibridomas/imunologia , Imunoglobulina A/biossíntese , Cadeias Pesadas de Imunoglobulinas/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Linfoma , Camundongos , Peso Molecular , Hibridização de Ácido Nucleico , Biossíntese de Proteínas , RNA Mensageiro/genética , Transcrição GênicaAssuntos
Clonagem Molecular , Cadeias Pesadas de Imunoglobulinas/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Cadeias gama de Imunoglobulina/biossíntese , Cadeias mu de Imunoglobulina/biossíntese , Plasmocitoma/imunologia , RNA Mensageiro/biossíntese , Animais , DNA/metabolismo , Enzimas de Restrição do DNA , Camundongos , Neoplasias Experimentais/imunologia , Hibridização de Ácido Nucleico , Plasmídeos , Poli A/biossíntese , Biossíntese de ProteínasRESUMO
Proliferating cells from twenty-four patients with alpha- or gamma-heavy chain disease (HCD) were studied by direct immunofluorescence and in several cases by biosynthesis experiments with 14C-amino acid incorporation. In twenty-two patients, the cells contained the HCD proteins only and no light chain synthesis could be detected. Conversely, apparently non-secreted monotypic light chains were found in one case of gamma-HCD and one case of alpha-HCD. The proportion of proliferating cells containing cytoplasmic heavy chains, their appearance and the presence or not of surface heavy chains showed great variation from patient to patient. In some cases, the proliferation predominantly affected either plasma cells or lymphocytes whereas in others the disease seemed to correspond to a proliferation of HCD protein-bearing lymphocytes with persistent maturation into plasma cells. Large cell lymphomas supervening on alpha-HCD belonged to the same proliferating clone as the clone secreting the HCD protein, as shown by surface markers and biosynthesis experiments which demonstrated synthesis but no secretion of HCD proteins. In one patient with gamma-HCD, the cells carried surface gamma and delta chains.
Assuntos
Doença das Cadeias Pesadas/imunologia , Cadeias Pesadas de Imunoglobulinas/análise , Cadeias Leves de Imunoglobulina/análise , Cadeias alfa de Imunoglobulina/análise , Cadeias gama de Imunoglobulina/análise , Adulto , Idoso , Criança , Humanos , Cadeias Leves de Imunoglobulina/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Cadeias gama de Imunoglobulina/biossíntese , Linfócitos/imunologia , Linfoma Difuso de Grandes Células B/imunologia , Pessoa de Meia-Idade , Plasmócitos/imunologia , Receptores de Antígenos de Linfócitos B/análiseAssuntos
Cadeias Pesadas de Imunoglobulinas/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , RNA Mensageiro , RNA , Linfócitos T/imunologia , Animais , Sequência de Bases , Linhagem Celular , Cadeias kappa de Imunoglobulina/biossíntese , Cinética , Camundongos , Desnaturação de Ácido Nucleico , Hibridização de Ácido Nucleico , Plasmocitoma , Biossíntese de Proteínas , RNA/metabolismo , RNA Mensageiro/metabolismo , Baço/imunologia , Timo/imunologiaRESUMO
Cells of the 315LV-1 (derived from NP1) variant line of MOPC 315 contain approximately 1% the normal intracellular level of the heavy (alpha) chain of IgA and no detectable light (lambda2) chain. The synthesis rate of alpha-chain in the variant, however, is similar to that in cells of the parent line. Moreover the relative amount of translatable alpha-chain mRNA that can be extracted from 315LV-1 cells is about the same as for parental cells. No light-chain synthesis can be detected either in vivo or in vitro in a wheat germ cell-free system. The 315LV-1 heavy chain synthesized in vivo or in vitro has slightly greater electrophoretic mobility than normal H chain and turns over rapidly intracellularly. The variant fails to secrete any of its heavy chain, despite the fact that its H chain mRNA is bound to membranes, as one would expect for a secretory protein message. Fusion of 315LV-1 cells with cells of a kappa-producing MPC 11 variant line leads to stabilization of the intracellular H chain and also to full recovery of secretion of the H chain as an H2L2 molecule.
Assuntos
Linhagem Celular , Cadeias Pesadas de Imunoglobulinas/biossíntese , Cadeias alfa de Imunoglobulina/biossíntese , Plasmocitoma/imunologia , Animais , Cadeias lambda de Imunoglobulina/biossíntese , Técnicas In Vitro , Camundongos , Camundongos Endogâmicos BALB C , Plasmocitoma/genética , RNA Mensageiro , RNA NeoplásicoRESUMO
Myeloma cells of the "wild type" that produce complete immunoglobulin molecules and those of the more usual variant type that display only one kind of chain [either light (L) or heavy (H)] were cocultivated ip and sc in syngeneic BALB/c mice. With each of six deliberately selected variants, a progressive increase in the proportion of wild-type cells was observed; the rate of change suggested that these variants had an approximately 10% slower growth rate than that of the wild-type tumor. In contrast, a variant that arose spontaneously overgrew the wild-type cells. The results may account for a) the stable capacity of most wild-type tumors to produce complete immunoglobulin molecules (L- plus H-chains) over many years, even though they frequently generate variant cells that produce only L- or only H-chains; and b) the occasional spontaneous change of myeloma cell populations from predominantly wild-type to variant cells.