RESUMO
To maintain polarity, epithelial cells continuously sort transmembrane proteins to the apical or basolateral membrane domains during biosynthetic delivery or after internalization. During biosynthetic delivery, some cargo proteins move from the trans-Golgi network (TGN) into recycling endosomes (RE) before being delivered to the plasma membrane. However, proteins that regulate this transport step remained elusive. In this study, we show that Rab13 partially colocalizes with TGN38 at the TGN and transferrin receptors in RE. Knockdown of Rab13 with short hairpin RNA in human bronchial epithelial cells or overexpression of dominant-active or dominant-negative alleles of Rab13 in Madin-Darby canine kidney cells disrupts TGN38/46 localization at the TGN. Moreover, overexpression of Rab13 mutant alleles inhibits surface arrival of proteins that move through RE during biosynthetic delivery (vesicular stomatitis virus glycoprotein [VSVG], A-VSVG, and LDLR-CT27). Importantly, proteins using a direct route from the TGN to the plasma membrane are not affected. Thus, Rab13 appears to regulate membrane trafficking between TGN and RE.
Assuntos
Endossomos/metabolismo , Células Epiteliais/metabolismo , Complexo de Golgi/metabolismo , Proteínas rab de Ligação ao GTP/fisiologia , Animais , Autoantígenos/metabolismo , Polaridade Celular , Células Cultivadas , Cães , Humanos , Glicoproteínas de Membrana/análise , Glicoproteínas de Membrana/metabolismo , Proteínas de Membrana/metabolismo , Mutação , Transporte Proteico/fisiologia , Receptores da Transferrina/análise , Receptores da Transferrina/metabolismo , Proteínas do Envelope Viral/metabolismo , Proteínas rab de Ligação ao GTP/análise , Proteínas rab de Ligação ao GTP/genéticaRESUMO
Similar to most differentiated cells, both neurons and epithelial cells elaborate distinct plasma membrane domains that contain different membrane proteins. We have previously shown that the axonal cell-adhesion molecule L1/NgCAM accumulates on the axonal surface by an indirect transcytotic pathway via somatodendritic endosomes. MDCK epithelial cells similarly traffic NgCAM to the apical surface by transcytosis. In this study, we map the signals in NgCAM required for routing via the multi-step transcytotic pathway. We identify both a previously mapped tyrosine-based signal as a sufficient somatodendritic targeting signal, as well as a novel axonal targeting signal in the cytoplasmic tail of NgCAM. The axonal signal is glycine and serine rich, but only the glycine residues are required for activity. The somatodendritic signal is cis-dominant and needs to be inactivated in order for the axonal signal to be executed. Additionally, we show that the axonal cytoplasmic signal promotes apical targeting in MDCK cells. Transcytosis of NgCAM to the axon thus requires the sequential regulated execution of multiple targeting signals.
Assuntos
Axônios/metabolismo , Moléculas de Adesão Celular Neurônio-Glia/metabolismo , Transdução de Sinais , Sequência de Aminoácidos , Animais , Moléculas de Adesão Celular Neurônio-Glia/química , Polaridade Celular , Galinhas , Dendritos/metabolismo , Cães , Endocitose , Células Epiteliais/citologia , Células Epiteliais/metabolismo , Glicina , Dados de Sequência Molecular , Alinhamento de Sequência , Serina , Rede trans-Golgi/metabolismoRESUMO
It has been demonstrated that large constructed wetlands used for domestic wastewater treatment are useful in the reduction of enteric microorganisms. This study evaluated the ability of three small-scale, on-site subsurface wetlands with different vegetation densities to remove total coliforms, fecal coliforms, coliphage, Giardia and Cryptosporidium. These wetlands were found to be equally efficient in the removal of enteric bacteria and coliphage as larger constructed wetlands. Giardia and Cryptosporidium were usually undetectable after passage of the wastewater through the subsurface wetlands. Coliphage removal increased with increasing vegetation density.