TY - JOUR
T1 - An unusual Fc receptor-related protein expressed in human centroblasts
AU - Facchetti, Fabio
AU - Cella, Marina
AU - Festa, Silvana
AU - Fremont, Daved H.
AU - Colonna, Marco
PY - 2002/3/19
Y1 - 2002/3/19
N2 - Here, we report the identification of Fc receptor homolog expressed in B cells (FREB), a unique B cell-specific molecule that is distantly related to FcγRI (receptor I for the Fc fragment of IgG) and is encoded on human chromosome 1q, within the FcγR gene region. FREB has an intracellular distribution and lacks a canonical transmembrane domain. In addition, FREB lacks bona fide Fc fragment binding regions and does not bind immunoglobulins. By using specific monoclonal antibodies, we show that FREB is preferentially expressed in germinal center centroblasts, which undergo affinity maturation and class-switch recombination. Together, these characteristics indicate that FREB may have a unique role in B cell differentiation. FREB is also expressed in some B cell lymphomas, most of which have centroblast origin. Remarkably, FREB is expressed in a subset of diffuse large B cell lymphomas, providing a unique marker for the characterization of this B cell malignancy.
AB - Here, we report the identification of Fc receptor homolog expressed in B cells (FREB), a unique B cell-specific molecule that is distantly related to FcγRI (receptor I for the Fc fragment of IgG) and is encoded on human chromosome 1q, within the FcγR gene region. FREB has an intracellular distribution and lacks a canonical transmembrane domain. In addition, FREB lacks bona fide Fc fragment binding regions and does not bind immunoglobulins. By using specific monoclonal antibodies, we show that FREB is preferentially expressed in germinal center centroblasts, which undergo affinity maturation and class-switch recombination. Together, these characteristics indicate that FREB may have a unique role in B cell differentiation. FREB is also expressed in some B cell lymphomas, most of which have centroblast origin. Remarkably, FREB is expressed in a subset of diffuse large B cell lymphomas, providing a unique marker for the characterization of this B cell malignancy.
UR - http://www.scopus.com/inward/record.url?scp=0037133665&partnerID=8YFLogxK
U2 - 10.1073/pnas.022042699
DO - 10.1073/pnas.022042699
M3 - Article
C2 - 11891275
AN - SCOPUS:0037133665
SN - 0027-8424
VL - 99
SP - 3776
EP - 3781
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 6
ER -