Dataset Information

InsP₃R-SEC5 interaction on phagosomes modulates innate immunity to Candida albicans by promoting cytosolic Ca²⁺ elevation and TBK1 activity.

ABSTRACT:

Background

Candida albicans (C. albicans) invasion triggers antifungal innate immunity, and the elevation of cytoplasmic Ca²⁺ levels via the inositol 1,4,5-trisphosphate receptor (InsP₃R) plays a critical role in this process. However, the molecular pathways linking the InsP₃R-mediated increase in Ca²⁺ and immune responses remain elusive.

Results

In the present study, we find that during C. albicans phagocytosis in macrophages, exocyst complex component 2 (SEC5) promotes InsP₃R channel activity by binding to its C-terminal α-helix (H1), increasing cytosolic Ca²⁺ concentrations ([Ca²⁺]_c). Immunofluorescence reveals enriched InsP₃R-SEC5 complex formation on phagosomes, while disruption of the InsP₃R-SEC5 interaction by recombinant H1 peptides attenuates the InsP₃R-mediated Ca²⁺ elevation, leading to impaired phagocytosis. Furthermore, we show that C. albicans infection promotes the recruitment of Tank-binding kinase 1 (TBK1) by the InsP₃R-SEC5 interacting complex, leading to the activation of TBK1. Subsequently, activated TBK1 phosphorylates interferon regulatory factor 3 (IRF-3) and mediates type I interferon responses, suggesting that the InsP₃R-SEC5 interaction may regulate antifungal innate immune responses not only by elevating cytoplasmic Ca²⁺ but also by activating the TBK1-IRF-3 pathway.

Conclusions

Our data have revealed an important role of the InsP₃R-SEC5 interaction in innate immune responses against C. albicans.

SUBMITTER: Yang L

PROVIDER: S-EPMC5921305 | biostudies-literature | 2018 Apr

REPOSITORIES: biostudies-literature

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Publications

InsP<sub>3</sub>R-SEC5 interaction on phagosomes modulates innate immunity to Candida albicans by promoting cytosolic Ca<sup>2+</sup> elevation and TBK1 activity.

Yang Long L Gu Wenwen W Cheung King-Ho KH Yan Lan L Tong Benjamin Chun-Kit BC Jiang Yuanying Y Yang Jun J

BMC biology 20180427 1

<h4>Background</h4>Candida albicans (C. albicans) invasion triggers antifungal innate immunity, and the elevation of cytoplasmic Ca<sup>2+</sup> levels via the inositol 1,4,5-trisphosphate receptor (InsP<sub>3</sub>R) plays a critical role in this process. However, the molecular pathways linking the InsP<sub>3</sub>R-mediated increase in Ca<sup>2+</sup> and immune responses remain elusive.<h4>Results</h4>In the present study, we find that during C. albicans phagocytosis in macrophages, exocyst c ...[more]

PMID: 29703257

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Project description:BackgroundThe postnatal mammalian ovary undergoes a series of changes to ensure the maturation of sufficient follicles to support ovulation and fecundation over the reproductive life. It is well known that intracellular [Ca2+]i signals are necessary for ovulation, fertilization, and egg activation. However, we lack detailed knowledge of the molecular identity, cellular distribution, and functional role of Ca2+ channels expressed during folliculogenesis. In the neonatal period, ovarian maturation is controlled by protein growth factors released from the oocyte and granulosa cells. Conversely, during the early infantile period, maturation becomes gonadotropin-dependent and is controlled by granulosa and theca cells. The significance of intracellular Ca2+ signaling in folliculogenesis is supported by the observation that mice lacking the expression of Ca2+/calmodulin-dependent kinase IV in granulosa cells suffer abnormal follicular development and impaired fertility.ResultsUsing immunofluorescence in frozen ovarian sections and confocal microscopy, we assessed the expression of high-voltage activated Ca2+ channel alpha subunits and InsP3 and ryanodine receptors in the postnatal period from 3 to 16 days. During the neonatal stage, oocytes from primordial and primary follicles show high expression of various Ca2+-selective channels, with granulosa and stroma cells expressing significantly less. These channels are likely involved in supporting Ca2+-dependent secretion of peptide growth factors. In contrast, during the early and late infantile periods, Ca2+ channel expression in the oocyte diminishes, increasing significantly in the granulosa and particularly in immature theca cells surrounding secondary follicles.ConclusionsThe developmental switch of Ca2+ channel expression from the oocytes to the perifollicular cells likely reflects the vanishing role of the oocytes once granulosa and theca cells take control of folliculogenesis in response to gonadotropins acting on their receptors.

Project description:Ca2+ signaling plays an essential role in T cell activation, which is a key step to start an adaptive immune response. During the transition from a quiescent to a fully activated state, Ca2+ microdomains characterized by reduced spatial and temporal extents are observed in the junctions between the plasma membrane (PM) and the endoplasmic reticulum (ER). Such Ca2+ responses can also occur in response to T cell adhesion to other cells or extracellular matrix proteins in otherwise unstimulated T cells. These non-TCR/CD3-dependent Ca2+ microdomains rely on d-myo-inositol 1,4,5-trisphosphate (IP3) signaling and subsequent store operated Ca2+ entry (SOCE) via the ORAI/STIM system. The detailed molecular mechanism of adhesion-dependent Ca2+ microdomain formation remains to be fully elucidated. We used mathematical modeling to investigate the spatiotemporal characteristics of T cell Ca2+ microdomains and their molecular regulators. We developed a reaction-diffusion model using COMSOL Multiphysics to describe the evolution of cytosolic and ER Ca2+ concentrations in a three-dimensional ER-PM junction. Equations are based on a previously proposed realistic description of the junction, which is extended to take into account IP3 receptors (IP3R) that are located next to the junction. The first model only considered the ORAI channels and the SERCA pumps. Taking into account the existence of preformed clusters of ORAI1 and STIM2, ORAI1 slightly opens in conditions of a full ER. These simulated Ca2+ microdomains are too small as compared to those observed in unstimulated T cells. When considering the opening of the IP3Rs located near the junction, the local depletion of ER Ca2+ allows for larger Ca2+ fluxes through the ORAI1 channels and hence larger local Ca2+ concentrations. Computational results moreover show that Ca2+ diffusion in the ER has a major impact on the Ca2+ changes in the junction, by affecting the local Ca2+ gradients in the sub-PM ER. Besides pointing out the likely involvement of the spontaneous openings of IP3Rs in the activation of SOCE in conditions of T cell adhesion prior to full activation, the model provides a tool to investigate how Ca2+ microdomains extent and interact in response to T cell receptor activation.

Dataset Information

InsP₃R-SEC5 interaction on phagosomes modulates innate immunity to Candida albicans by promoting cytosolic Ca²⁺ elevation and TBK1 activity.

Background

Results

Conclusions

Publications

InsP<sub>3</sub>R-SEC5 interaction on phagosomes modulates innate immunity to Candida albicans by promoting cytosolic Ca<sup>2+</sup> elevation and TBK1 activity.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets

Dataset Information

InsP3R-SEC5 interaction on phagosomes modulates innate immunity to Candida albicans by promoting cytosolic Ca2+ elevation and TBK1 activity.

Background

Results

Conclusions

Publications

InsP<sub>3</sub>R-SEC5 interaction on phagosomes modulates innate immunity to Candida albicans by promoting cytosolic Ca<sup>2+</sup> elevation and TBK1 activity.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets

InsP₃R-SEC5 interaction on phagosomes modulates innate immunity to Candida albicans by promoting cytosolic Ca²⁺ elevation and TBK1 activity.