Literature DB >> 1378867

Role of I-A molecules in early stages of B cell maturation.

N Miki1, M Hatano, K Wakita, S Imoto, S Nishikawa, S Nishikawa, T Tokuhisa.   

Abstract

The role of the Ia molecule in the early phase of B cell development remains controversial. In contrast to previous studies, we have detected minute amounts of Ia (I-A) molecule on early B lineage (B220+IgM-) cells from normal bone marrow, using ELISA. The presence of the I-A molecule even on pro-B cells was deduced from experiments in which a monoclonal anti-I-A antibody completely blocked the generation of pre-B cells from B progenitor (B220-) cells in stromal cell-dependent B cell culture. Inasmuch as this antibody did not inhibit the maturation of pre-B cells to IgM+ B cells in culture, the I-A molecule on early B lineage cells probably plays a role in their maturation. We also examined the role of the I-A molecule in early B cell development, using transgenic mice harboring the antisense DNA to I-A beta-chain gene. The amount of I-A molecule on splenic B cells from the young transgenic mice decreased in the presence of abundant amounts of the antisense RNA. B cell development was perturbed in spleen from the transgenic mice. Stromal cell-dependent B cell cultures from these mice clearly showed that the maturation of B lineage cells was delayed at a very early stage of development (B220- to B220+). We propose that the I-A molecule on early B lineage cells may play an essential role in their maturation.

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Year:  1992        PMID: 1378867

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  5 in total

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Review 2.  Antisense and ribozyme constructs in transgenic animals.

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Journal:  Transgenic Res       Date:  1996-11       Impact factor: 2.788

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Authors:  Kelly A Cycon; James L Clements; Renae Holtz; Hiroshi Fuji; Shawn P Murphy
Journal:  Immunology       Date:  2009-01-12       Impact factor: 7.397

4.  Developmental extinction of major histocompatibility complex class II gene expression in plasmocytes is mediated by silencing of the transactivator gene CIITA.

Authors:  P Silacci; A Mottet; V Steimle; W Reith; B Mach
Journal:  J Exp Med       Date:  1994-10-01       Impact factor: 14.307

5.  Major histocompatibility complex class II expression distinguishes two distinct B cell developmental pathways during ontogeny.

Authors:  K P Lam; A M Stall
Journal:  J Exp Med       Date:  1994-08-01       Impact factor: 14.307

  5 in total

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