Cargando…

Alteration of Intestinal Microbiota Composition in Oral Sensitized C3H/HeJ Mice Is Associated With Changes in Dendritic Cells and T Cells in Mesenteric Lymph Nodes

This research aimed to investigate the allergic reaction of C3H/HeJ mice after sensitization with ovalbumin (OVA) without any adjuvant and to analyze the association between intestinal microbiota and allergy-related immune cells in mesenteric lymph nodes (MLN). The allergic responses of C3H/HeJ mice...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhou, Cui, Chen, Ling-Ling, Lu, Rui-Qi, Ma, Wei-Wei, Xiao, Rong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Immunology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222730/ https://www.ncbi.nlm.nih.gov/pubmed/34177885 http://dx.doi.org/10.3389/fimmu.2021.631494

Ejemplares similares

Lack of oral tolerance in C3H/HeJ mice
Publicado: (1982)

Generalized resistance to pruritogen-induced scratching in the C3H/HeJ strain
por: Zhang, Yanbin, et al.
Publicado: (2022)

Endotoxin protein: a B-cell mitogen and polyclonal activator of C3H/HeJ lymphocytes
Publicado: (1976)

Suppression of the immune response in C3H/HeJ mice by protein-free lipopolysaccharides
Publicado: (1978)

A new mutation, gld, that produces lymphoproliferation and autoimmunity in C3H/HeJ mice
Publicado: (1984)

Defective colony formation by B lymphocytes from CBA/N and C3H/HeJ mice
Publicado: (1977)

Inflammatory Signatures of Pathogenic and Non-Pathogenic Leptospira Infection in Susceptible C3H-HeJ Mice
por: Shetty, Advait, et al.
Publicado: (2021)

NLRP3 inflammasome activation contributes to development of alopecia areata in C3H/HeJ mice
por: Hashimoto, Kei, et al.
Publicado: (2021)

Isolation of a lipid a bound polypeptide responsible for “LPS- initiated” mitogenesis of C3H/HeJ spleen cells
por: Morrison, DC, et al.
Publicado: (1976)

A Discrete Subpopulation of Dendritic Cells Transports Apoptotic Intestinal Epithelial Cells to T Cell Areas of Mesenteric Lymph Nodes
por: Huang, Fang-Ping, et al.
Publicado: (2000)

Lack of response to laser comb in spontaneous and graft induced alopecia areata in C3H/HeJ mice
por: King, Lloyd E., et al.
Publicado: (2013)

Novel Bivalent and D-Peptide Ligands of CXCR4 Mobilize Hematopoietic Progenitor Cells to the Blood in C3H/HeJ Mice
por: Mao, Yujia, et al.
Publicado: (2018)

Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4
por: Beyer, Barbara, et al.
Publicado: (2008)

Development of Autoimmune Hair Loss Disease Alopecia Areata Is Associated with Cardiac Dysfunction in C3H/HeJ Mice
por: Wang, Eddy, et al.
Publicado: (2013)

TLR4‐defective (C3H/HeJ) mice are not protected from cast immobilization‐induced muscle atrophy
por: Kawanishi, Noriaki, et al.
Publicado: (2017)

Neonatally imprinted stromal cell subsets induce tolerogenic dendritic cells in mesenteric lymph nodes
por: Pezoldt, Joern, et al.
Publicado: (2018)

Excision of mesenteric lymph nodes alters gut microbiota and impairs social dominance in adult mice
por: Yang, Rui, et al.
Publicado: (2023)

The Effect of Transplanted Methylcholanthrene Induced Fibrosarcomata and Corynebacterium parvum on the Immune Response of CBA and A/HeJ Mice to Thymus Dependent and Independent Antigens
por: James, K., et al.
Publicado: (1974)

Immunologic responsiveness of the C3H/HeJ mouse: differential ability of butanol-extracted lipopolysaccharide (LPS) to evoke LPS-mediated effects
Publicado: (1978)

Induction of alopecia areata in C3H/HeJ mice using polyinosinic-polycytidylic acid (poly[I:C]) and interferon-gamma
por: Shin, Jung-Min, et al.
Publicado: (2018)

Corticotropin-releasing Factor Changes the Phenotype and Function of Dendritic Cells in Mouse Mesenteric Lymph Nodes
por: Meng, Li, et al.
Publicado: (2015)

Contribution of Mesenteric Lymph Nodes and GALT to the Intestinal Foxp3+ Regulatory T-Cell Compartment
por: Geem, Duke, et al.
Publicado: (2016)

17beta-oestradiol and Enovid mammary tumorigenesis in C3H/HeJ female mice: counteraction by concurrent 2-bromo-alpha-ergocryptine.
por: Welsch, C. W., et al.
Publicado: (1977)

The microbiota is dispensable for the early stages of peripheral regulatory T cell induction within mesenteric lymph nodes
por: Wiechers, Carolin, et al.
Publicado: (2021)

Age-Related Reference Intervals of the Main Biochemical and Hematological Parameters in C57BL/6J, 129SV/EV and C3H/HeJ Mouse Strains
por: Mazzaccara, Cristina, et al.
Publicado: (2008)

Evaluation of Mesenteric Lymph Nodes in a Pediatric Population with Mesenteric Lymphadenitis Using Superb Microvascular Imaging
por: Zu, Dao-Ming, et al.
Publicado: (2019)

Selective Expansion of Tregs Using the IL-2 Cytokine Antibody Complex Does Not Reverse Established Alopecia Areata in C3H/HeJ Mice
por: Lee, Eunjin, et al.
Publicado: (2022)

Single-cell transcriptomics reveals striking heterogeneity and functional organization of dendritic and monocytic cells in the bovine mesenteric lymph node
por: Barut, Güliz Tuba, et al.
Publicado: (2023)

Immunologic properties of bacterial lipopolysaccharide (LPS). II. The unresponsiveness of C3H/HeJ Mouse spleen cells to LPS-induced mitogenesis is dependent on the method used to extract LPS
Publicado: (1975)

Microbiota Restrict Trafficking of Bacteria to Mesenteric Lymph Nodes by CX(3)CR1(hi) Cells
por: Diehl, Gretchen E., et al.
Publicado: (2013)

Fecal and Tissue Microbiota Are Associated with Tumor T-Cell Infiltration and Mesenteric Lymph Node Involvement in Colorectal Cancer
por: Luu, Kayti, et al.
Publicado: (2023)

Age-Dependent Decrease in the Induction of Regulatory T Cells Is Associated With Decreased Expression of RALDH2 in Mesenteric Lymph Node Dendritic Cells
por: Takano, Tomohiro, et al.
Publicado: (2020)

Mesenteric lymph nodes at the center of immune anatomy
por: Macpherson, Andrew J., et al.
Publicado: (2006)

Lack of Association between the Tlr4 (Lps(d)/Lps(d)) Genotype and Increased Susceptibility to Escherichia coli Bladder Infections in Female C3H/HeJ Mice
por: Suhs, Kaleigh A., et al.
Publicado: (2011)

Association of lymph node metastases, grade and extent of mesenteric lymph node dissection in locoregional small intestinal neuroendocrine tumors with recurrence‐free survival
por: Daskalakis, Kosmas, et al.
Publicado: (2022)

Accumulation of eosinophils in intestine-draining mesenteric lymph nodes occurs after Trichuris muris infection
por: SVENSSON, M, et al.
Publicado: (2011)

Stromal mesenteric lymph node cells are essential for the generation of gut-homing T cells in vivo
por: Hammerschmidt, Swantje I., et al.
Publicado: (2008)

Abnormal Thyroid Hormone Status Differentially Affects Bone Mass Accrual and Bone Strength in C3H/HeJ Mice: A Mouse Model of Type I Deiodinase Deficiency
por: Zaitune, Clarissa R., et al.
Publicado: (2019)

Regulation of lymph node vascular growth by dendritic cells
por: Webster, Brian, et al.
Publicado: (2006)

Evaluation of the long-term skeletal effect induced by teratogen 5-aza-2′deoxycytidine on offspring of high (C3H/HeJ) and low (C57BL/6J) bone mass phenotype mice
por: Khajuria, Deepak Kumar, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_sabm99kbbhu5jddphfmpcntl2i