RESUMO
Dendritic cells (DCs) sample peripheral tissues of the body in search of antigens to present to T cells. This requires two processes, antigen processing and cell motility, originally thought to occur independently. We found that the major histocompatibility complex II-associated invariant chain (Ii or CD74), a known regulator of antigen processing, negatively regulates DC motility in vivo. By using microfabricated channels to mimic the confined environment of peripheral tissues, we found that wild-type DCs alternate between high and low motility, whereas Ii-deficient cells moved in a faster and more uniform manner. The regulation of cell motility by Ii depended on the actin-based motor protein myosin II. Coupling antigen processing and cell motility may enable DCs to more efficiently detect and process antigens within a defined space.
Assuntos
Antígenos de Diferenciação de Linfócitos B/metabolismo , Movimento Celular , Células Dendríticas/imunologia , Antígenos de Histocompatibilidade Classe II/metabolismo , Miosina Tipo II/metabolismo , Animais , Apresentação de Antígeno , Antígenos de Diferenciação de Linfócitos B/genética , Catepsinas/genética , Catepsinas/metabolismo , Células Dendríticas/fisiologia , Endocitose , Antígenos de Histocompatibilidade Classe II/genética , Lipopolissacarídeos/imunologia , Linfonodos/citologia , Linfonodos/imunologia , Lisossomos/metabolismo , Camundongos , Camundongos Endogâmicos C57BL , FosforilaçãoRESUMO
Antigen binding to the B-cell receptor (BCR) induces multiple signaling cascades that ultimately lead to B lymphocyte activation. In addition, the BCR regulates the key trafficking events that allow the antigen to reach endocytic compartments devoted to antigen processing, i.e., that are enriched for major histocompatibility factor class II (MHC II) and accessory molecules such as H2-DM. Here, we analyze the role in antigen processing and presentation of the tyrosine kinase Syk, which is activated upon BCR engagement. We show that convergence of MHC II- and H2-DM-containing compartments with the vesicles that transport BCR-uptaken antigens is impaired in cells lacking Syk activity. This defect in endocytic trafficking compromises the ability of Syk-deficient cells to form MHC II-peptide complexes from BCR-internalized antigens. Altered endocytic trafficking is associated to a failure of Syk-deficient cells to properly reorganize their actin cytoskeleton in response to BCR engagement. We propose that, by modulating the actin dynamics induced upon BCR stimulation, Syk regulates the positioning and transport of the vesicles that carry the molecules required for antigen processing and presentation.
Assuntos
Actinas/metabolismo , Apresentação de Antígeno/imunologia , Endocitose , Peptídeos e Proteínas de Sinalização Intracelular/metabolismo , Proteínas Tirosina Quinases/metabolismo , Receptores de Antígenos de Linfócitos B/metabolismo , Animais , Linhagem Celular Tumoral , Citoesqueleto/metabolismo , Antígenos de Histocompatibilidade Classe II/metabolismo , Peptídeos e Proteínas de Sinalização Intracelular/deficiência , Ativação Linfocitária , Lisossomos/metabolismo , Lisossomos/ultraestrutura , Camundongos , Peptídeos/metabolismo , Transporte Proteico , Proteínas Tirosina Quinases/deficiência , Proteínas Tirosina Quinases/ultraestrutura , Baço/citologia , Baço/metabolismo , Quinase SykRESUMO
Antigen (Ag) capture and presentation onto major histocompatibility complex (MHC) class II molecules by B lymphocytes is mediated by their surface Ag receptor (B cell receptor [BCR]). Therefore, the transport of vesicles that carry MHC class II and BCR-Ag complexes must be coordinated for them to converge for processing. In this study, we identify the actin-associated motor protein myosin II as being essential for this process. Myosin II is activated upon BCR engagement and associates with MHC class II-invariant chain complexes. Myosin II inhibition or depletion compromises the convergence and concentration of MHC class II and BCR-Ag complexes into lysosomes devoted to Ag processing. Accordingly, the formation of MHC class II-peptides and subsequent CD4 T cell activation are impaired in cells lacking myosin II activity. Therefore, myosin II emerges as a key motor protein in BCR-driven Ag processing and presentation.
Assuntos
Apresentação de Antígeno/imunologia , Linfócitos B/metabolismo , Antígenos de Histocompatibilidade Classe II/metabolismo , Miosina Tipo II/metabolismo , Receptores de Antígenos de Linfócitos B/metabolismo , Vesículas Transportadoras/metabolismo , Actinas/metabolismo , Animais , Linfócitos B/imunologia , Linfócitos T CD4-Positivos/imunologia , Células Cultivadas , Antígenos de Histocompatibilidade Classe II/imunologia , Ativação Linfocitária/imunologia , Lisossomos/imunologia , Lisossomos/metabolismo , Substâncias Macromoleculares/imunologia , Substâncias Macromoleculares/metabolismo , Camundongos , Camundongos Transgênicos , Miosina Tipo II/imunologia , Transporte Proteico/imunologia , Receptores de Antígenos de Linfócitos B/imunologia , Vesículas Transportadoras/imunologiaRESUMO
Antigen capture and presentation onto MHC class II molecules by B lymphocytes is mediated by their surface antigen receptor - the B-cell receptor (BCR). The BCR must therefore coordinate the transport of MHC class II- and antigen-containing vesicles for them to converge and ensure efficient processing. Recently, progress has been made in understanding which and how these vesicular transport events are molecularly linked to BCR signaling. In particular, recent studies have emphasized the key roles of membrane microdomains and the actin cytoskeleton in regulation of membrane trafficking upon BCR engagement.