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1.
Immunity ; 57(5): 1056-1070.e5, 2024 May 14.
Artículo en Inglés | MEDLINE | ID: mdl-38614091

RESUMEN

A specialized population of mast cells residing within epithelial layers, currently known as intraepithelial mast cells (IEMCs), was originally observed over a century ago, yet their physiological functions have remained enigmatic. In this study, we unveil an unexpected and crucial role of IEMCs in driving gasdermin C-mediated type 2 immunity. During helminth infection, αEß7 integrin-positive IEMCs engaged in extensive intercellular crosstalk with neighboring intestinal epithelial cells (IECs). Through the action of IEMC-derived proteases, gasdermin C proteins intrinsic to the epithelial cells underwent cleavage, leading to the release of a critical type 2 cytokine, interleukin-33 (IL-33). Notably, mast cell deficiency abolished the gasdermin C-mediated immune cascade initiated by epithelium. These findings shed light on the functions of IEMCs, uncover a previously unrecognized phase of type 2 immunity involving mast cell-epithelial cell crosstalk, and advance our understanding of the cellular mechanisms underlying gasdermin C activation.


Asunto(s)
Interleucina-33 , Mastocitos , Proteínas de Unión a Fosfato , Mastocitos/inmunología , Mastocitos/metabolismo , Animales , Interleucina-33/metabolismo , Interleucina-33/inmunología , Ratones , Proteínas de Unión a Fosfato/metabolismo , Células Epiteliales/inmunología , Células Epiteliales/metabolismo , Ratones Endogámicos C57BL , Ratones Noqueados , Mucosa Intestinal/inmunología , Mucosa Intestinal/metabolismo , Péptidos y Proteínas de Señalización Intracelular/metabolismo , Péptidos y Proteínas de Señalización Intracelular/inmunología , Comunicación Celular/inmunología
2.
Appl Opt ; 62(19): 5159-5169, 2023 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-37707219

RESUMEN

In digital holography, the speckle noise caused by the coherent nature of the light source and the light scattering generated by the light path system degrade the quality of the reconstructed image seriously. Therefore, in this paper, we propose what we believe to be is a novel noise reduction method combining bidimensional empirical mode decomposition (BEMD) with the variational method, termed BEMDV. The reconstructed image is first decomposed into a series of bidimensional intrinsic mode function (BIMF) components with different frequencies using the BEMD method, and then a certain number of BIMF components are selected for noise reduction by the variational method. An improved particle swarm optimization algorithm is adopted to optimize the key parameters of the proposed method, so as to further improve its noise reduction performance. A reflective off-axis digital holographic imaging system is used to collect the holograms of the coin and optical resolution plate, and the experimental research on noise reduction is carried out. The results with qualitative and quantitative analyses show that the proposed method achieves a better performance on noise reduction and detail preservation than other general methods, enormously enhancing the image quality of holographic reconstruction.

3.
Adv Immunol ; 145: 129-157, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32081196

RESUMEN

Immune responses are often accompanied by radical changes of cellular metabolism of immune cells. On the other hand, an ever increasing number of metabolic pathways and products have been found to possess immune regulatory functions. The field of immunometabolism that investigates the interplay between metabolism and immunity has developed rapidly during the past decade. In this chapter, we attempt to summarize the recent progresses by scientists in China on metabolic regulation of innate immunity from the following three perspectives: metabolic regulation of myeloid cell functions, metabolic adaptations of tissue resident myeloid cells, and metabolism and immunity at the mucosal surfaces.


Asunto(s)
Metabolismo Energético/inmunología , Inmunidad Innata , Redes y Vías Metabólicas/inmunología , Células Mieloides/inmunología , Tejido Adiposo/citología , Tejido Adiposo/inmunología , Tejido Adiposo/metabolismo , Animales , Metabolismo Energético/genética , Hígado Graso/inmunología , Hígado Graso/metabolismo , Humanos , Mucosa Intestinal/citología , Mucosa Intestinal/inmunología , Mucosa Intestinal/metabolismo , Macrófagos del Hígado/inmunología , Macrófagos del Hígado/metabolismo , Macrófagos/inmunología , Macrófagos/metabolismo , Redes y Vías Metabólicas/genética , Células Mieloides/metabolismo , Microambiente Tumoral/genética , Microambiente Tumoral/inmunología
4.
Front Immunol ; 11: 2065, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-33013873

RESUMEN

In addition to their established functions in host defense, accumulating evidence has suggested an emerging role for antimicrobial proteins (AMPs) in shaping commensal microbiota. However, the role of α-defensins, the most abundant AMPs of intestine, in regulating microbial ecology remains inconclusive. Here, we report that α-defensins promote commensal Bacteroides colonization by enhancing bacterial adhesion to the mucosal reservoir. Experiments utilizing mice deficient in matrix metalloproteinase 7 (MMP7), the α-defensin-activating enzyme, with rigorous littermate controls showed that α-defensin deficiency did not significantly influence steady-state intestinal microbiota. In contrast, α-defensins are essential for replenishment of commensal Bacteroides from the mucosal reservoir following antibiotics-induced dysbiosis, shown by markedly compromised recovery of Bacteroides in Mmp7-/- animals. Mechanistically, α-defensins promote Bacteroides colonization on epithelial surfaces in vivo and adhesion to epithelial cells in vitro. Moreover, α-defensins unexpectedly does not show any microbicidal activities against Bacteroides. Together, we propose that α-defensins promote commensal bacterial colonization and recovery to maintain microbial diversity upon environmental challenges.


Asunto(s)
Antibacterianos/efectos adversos , Infecciones por Bacteroides/inmunología , Bacteroides/fisiología , Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos/inmunología , Disbiosis/inmunología , Mucosa Intestinal/inmunología , alfa-Defensinas/metabolismo , Animales , Antibacterianos/uso terapéutico , Homeostasis , Metaloproteinasa 7 de la Matriz/genética , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , ARN Ribosómico 16S/genética , Simbiosis
5.
Cell Host Microbe ; 25(5): 706-718.e7, 2019 05 08.
Artículo en Inglés | MEDLINE | ID: mdl-31053533

RESUMEN

Metabolic programs and host defense are highly integrated to ensure proper immune responses during stress. Central to these responses, mTOR regulates immune functions by sensing and integrating environmental cues, yet how these systems are coordinated at the intestinal surface remains undefined. We show that the antimicrobial peptide α-defensin is functionally sustained during nutrient deprivation because of regulation of the defensin-processing enzyme MMP7 by microbiota- and host-derived factors. Unlike other antimicrobial peptides, the MMP7-α-defensin axis remains active during nutrient fluctuations, providing essential protection against enteric pathogens. Sustained Mmp7 expression requires the microbiota and is mediated by de-repression of the transcription activator Atoh1 upon attenuation of the transcriptional repressor Hes1 in intestinal epithelial cells. Hes1 levels are regulated via mTOR and controlled translationally, constituting a metabolism-translation-transcription loop. Disrupting this loop by supplying nutrients paradoxically compromises antibacterial defense. Together, these results uncover a regulatory circuit that couples host nutrient status to epithelial antimicrobial immunity.


Asunto(s)
Células Epiteliales/inmunología , Regulación de la Expresión Génica , Inmunidad Mucosa , Metaloproteinasa 7 de la Matriz/biosíntesis , Nutrientes/metabolismo , Factor de Transcripción HES-1/metabolismo , alfa-Defensinas/biosíntesis , Animales , Línea Celular , Células Epiteliales/efectos de los fármacos , Mucosa Intestinal/efectos de los fármacos , Mucosa Intestinal/inmunología , Ratones Endogámicos C57BL
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