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Journal ArticleDOI

Contribution of B-1 Cells to Intestinal IgA Production in the Mouse

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TLDR
The data presented here show that, in principle, B-1 cells located in the peritoneal cavity may be an important source of precursors for intestinal IgA plasma cells in the mouse.
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This article is published in Methods.The article was published on 1995-08-01. It has received 22 citations till now. The article focuses on the topics: CD40 & Adoptive cell transfer.

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Journal ArticleDOI

Cyclins D1 and D2 mediate Myc‐induced proliferation via sequestration of p27Kip1 and p21Cip1

TL;DR: The sequestration function of D cyclins appears essential for Myc‐induced cell cycle progression but dispensable for apoptosis.
Journal Article

Biological Impact of Natural COOH-Terminal Deletions of Hepatitis B Virus X Protein in Hepatocellular Carcinoma Tissues

TL;DR: This study further supports the hypothesis that natural HBx mutants might be selected in tumor tissues and play a role in hepatocarcinogenesis by modifying the biological functions of HBx.
Journal ArticleDOI

The ATM-related domain of TRRAP is required for histone acetyltransferase recruitment and Myc-dependent oncogenesis

TL;DR: It is demonstrated that the ATM-related domain of TRRAP forms a structural core for the assembly and recruitment of HAT complexes by transcriptional activators.
Journal ArticleDOI

B1 cells contribute to serum IgM, but not to intestinal IgA, production in gnotobiotic Ig allotype chimeric mice

TL;DR: Data suggest that intestinal IgA production induced by commensal bacteria is mainly performed by B2, not B1, cells, which might play a similar role in mucosal immunity.
Journal ArticleDOI

Monoclonal immunoglobulin A derived from peritoneal B cells is encoded by both germ line and somatically mutated VH genes and is reactive with commensal bacteria.

TL;DR: Six to eight months after injection, only cells with the B1 phenotype were retained in the spleens and peritoneal cavities of these mice, and all the hybridomas reacted with different but partially overlapping fecal bacterial populations.
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