Immune Netw.  2004 Sep;4(3):155-160. 10.4110/in.2004.4.3.155.

B-1 Cells Differ from Conventional B (B-2) Cells: Difference in Proliferation

Affiliations
  • 1Department of Otolaryngology, College of Medicine, Kyung Hee University, Seoul, Korea.
  • 2Department of Obstetric and Gynecology, College of Medicine, Catholic University, Suwon, Korea. dcpark@catholic.ac.kr
  • 3Department of Medicine, School of Medicine and Immunobiology Unit, Evans Memorial Department of Clinical Research, Medical Center, Boston University, USA.

Abstract

BACKGROUND
B-1 cells differ from conventional B-2 cells both phenotypically and functionally. The aim of this study was to investigate the difference between peritoneal B-1 cells and splenic B-2 cells in proliferation. METHODS: We obtained sorted B-1 cells from peritoneal fluid and B-2 cells from spleens of mice. During the culture of these cells, immunoglobulin secreted into the culture supernatants was evaluated by enzyme- linked immunosorbent assay. Entering of S phase in response to LPS-stimuli was measured by proliferative assay. RESULTS: Spontaneous Immunoglobulin M production occurred in peritoneal B-1 cells but not in splenic B-2 cells. LPS stimulated peritoneal B-1 cells secreted IgM at day 1, but splenic B-2 cells at day 2. In thymidine incorporation, peritoneal B-1 cells entered actively S phase after 24hours LPS-stimulation but splenic B-2 cells entered actively S phase after 48 hours. CONCLUSION: IgM secretion and S phase entering occurred early in peritoneal B-1 cells compared to splenic B-2 cells.

Keyword

Peritoneal B-1 cell; splenic B-2 cell; immunoglobulin.proliferation

MeSH Terms

Animals
Ascitic Fluid
Immunoglobulin M
Immunoglobulins
Mice
S Phase
Spleen
Thymidine
Immunoglobulin M
Immunoglobulins
Thymidine
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