Cited by 783T-cell and B-cell ImmunologyCytokine Signaling Pathways and InteractionsNF-κB Signaling Pathways

The essential role of B cell stimulatory factor 2 (BSF-2/IL-6) for the terminal differentiation of B cells

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Muraguchi, A, Hirano, T, Tang, B, Matsuda, T, Horii, Y, Nakajima, K, Kishimoto, T·1988·The Journal of experimental medicine

Abstract

The role of recombinant B cell stimulatory factor 2 (BSF-2/IL-6) in the regulation of growth and differentiation of B cells was investigated. rBSF-2 at 200 pg/ml could induce 50% of the maximum Ig production in B lymphoblastoid cell lines, the specific activity being estimated as 5 X 10(6) U/mg. rBSF-2 augmented PWM-induced IgM, IgG, and IgA production in mononuclear cells (MNC); the effect was exerted by directly acting on PWM-induced B blast cells to induce Ig production. However, rBSF-2 did not induce any growth of activated B cells. In contrast, rBSF-2 showed a potent growth activity on a murine hybridoma clone, MH60.BSF2. The concentration required for half-maximal [3H]TdR uptake was approximately 5 pg/ml, which was 40 times less than that required for Ig induction in a B cell line. Anti-BSF-2 antibody inhibited PWM-induced Ig production in MNC, but not PWM-induced proliferation. The antibody was effective even when added on day 4 of an 8-d culture, indicating that BSF-2 is one of the essential late-acting factors in PWM-induced Ig production.

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Crossref · 10.1084/jem.167.2.332

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  • IL-6 promotes antibody production by directly acting on plasma cells and by indirectly promoting Bcl6-dependent follicular CD4+ T (Tfh) cell differentiation together with IL-21.

    “Indeed, IL-6 promotes antibody production by directly acting on plasma cells and by indirectly promoting Bcl6-dependent follicular CD4(+) T (Tfh) cell differentiation together with IL-21 (Fig. 2) (143–146).”

    From IL-6 in inflammation, autoimmunity and cancer (2021) · cites this paper as [143]

    The paper’s summary reports that IL-6 (BSF-2) directly acts on PWM-induced B blast cells to induce immunoglobulin production, supporting the direct antibody-production component. It does not establish direct action on plasma cells or address Bcl6-dependent Tfh differentiation or cooperation with IL-21. (LLM, conf=0.87)

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Authors
Muraguchi, A., Hirano, T., Tang, B., Matsuda, T., Horii, Y., Nakajima, K., & Kishimoto, T.
Affiliations
The University of Osaka (JP)
Venue
The Journal of experimental medicine
Published
1988-02-01
Volume
167
Issue
2
Pages
332-344
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2168822788
Cited by
783
References
0
Citations by year
2026: 3 · 2025: 4 · 2024: 11 · 2023: 14 · 2022: 14 · 2021: 10 · 2020: 13 · 2019: 12 · 2018: 4 · 2017: 13 · 2016: 13 · 2015: 7 · 2014: 15 · 2013: 18 · 2012: 15
FWCI
31.85
Type
journal article
Language
en
Open access
Locations
  • The Journal of Experimental Medicine (publishedVersion)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Health Sciences › Medicine › Oncology › Cytokine Signaling Pathways and Interactions
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
Keywords
B cell stimulatory factor 2, interleukin-6, B cell terminal differentiation, antibody production, B-lymphoblastoid cell lines, B cell proliferation, mononuclear cells
MeSH terms
Antibodies, B-Lymphocytes, Cell Differentiation, Cell Line, Transformed, Humans, Hybridomas, Immunoglobulins, Interleukins, Lymphocyte Activation, Pokeweed Mitogens, Recombinant Proteins, Interleukin-4

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