Commitment to the B lymphoid lineage occurs before DH-JH recombination

被引:100
作者
Allman, D [1 ]
Li, J [1 ]
Hardy, RR [1 ]
机构
[1] Fox Chase Canc Ctr, Inst Canc Res, Philadelphia, PA 19111 USA
关键词
lineage restriction; B lymphopoiesis; progenitor; hematopoiesis; stem cell;
D O I
10.1084/jem.189.4.735
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Lineage commitment in B lymphopoiesis remains poorly understood due to the inability to clearly define newly committed B lineage progenitors and their multipotential descendants. We examined the potential of three recently described progenitor populations in adult mouse bone marrow to differentiate into each hematopoietic lineage. The earliest of these, termed fraction (Fr.) A(0), exhibited myeloid, erythroid, and B and T lymphoid progenitor activity and included individual cells with myeloid/B lymphoid potential. In sharp contrast, two later populations, termed Frs. A(1) and A(2) and characterized by surface B220 expression and transcription of the germline immunoglobulin heavy chain (IgH) locus, lacked progenitor activity for all hematopoietic lineages except B lymphocytes. These observations, together with single cell polymerase chain reaction analysis showing a lack of D-H/J(H) rearrangements in each population and experiments showing identical precursor potentials when these populations were derived from recombination activating gene (Rag)-1(-/-) and J(H)(-/-) mice, demonstrate that commitment to the B lymphoid lineage occurs before and independently of V(H)D(H)J(H) recombination.
引用
收藏
页码:735 / 740
页数:6
相关论文
共 29 条
[1]
ANTICA M, 1994, BLOOD, V84, P111
[2]
Both E12 and E47 allow commitment to the B cell lineage [J].
Bain, G ;
Maandag, ECR ;
Riele, HPJT ;
Feeney, AJ ;
Sheehy, A ;
Schlissel, M ;
Shinton, SA ;
Hardy, RR ;
Murre, C .
IMMUNITY, 1997, 6 (02) :145-154
[3]
CHERVENAK R, 1993, J IMMUNOL, V151, P4486
[4]
ENRICHMENT AND CHARACTERIZATION OF UNCOMMITTED B-CELL PRECURSORS FROM FETAL LIVER AT DAY 12 OF GESTATION [J].
CUMANO, A ;
PAIGE, CJ .
EMBO JOURNAL, 1992, 11 (02) :593-601
[5]
BIPOTENTIAL PRECURSORS OF B-CELLS AND MACROPHAGES IN MURINE FETAL LIVER [J].
CUMANO, A ;
PAIGE, CJ ;
ISCOVE, NN ;
BRADY, G .
NATURE, 1992, 356 (6370) :612-615
[6]
ANALYSIS OF THE B-CELL PROGENITOR COMPARTMENT AT THE LEVEL OF SINGLE CELLS [J].
EHLICH, A ;
MARTIN, V ;
MULLER, W ;
RAJEWSKY, K .
CURRENT BIOLOGY, 1994, 4 (07) :573-583
[7]
RESOLUTION AND CHARACTERIZATION OF PRO-B AND PRE-PRO-B CELL STAGES IN NORMAL MOUSE BONE-MARROW [J].
HARDY, RR ;
CARMACK, CE ;
SHINTON, SA ;
KEMP, JD ;
HAYAKAWA, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (05) :1213-1225
[8]
MURINE HEMATOPOIETIC-CELLS WITH PRE-B OR PRE-B/MYELOID CHARACTERISTICS ARE GENERATED BY INVITRO TRANSFORMATION WITH RETROVIRUSES CONTAINING FES, RAS, ABL, AND SRC ONCOGENES [J].
HOLMES, KL ;
PIERCE, JH ;
DAVIDSON, WF ;
MORSE, HC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 164 (02) :443-457
[9]
CELLULAR AND DEVELOPMENTAL PROPERTIES OF FETAL HEMATOPOIETIC STEM-CELLS [J].
JORDAN, CT ;
MCKEARN, JP ;
LEMISCHKA, IR .
CELL, 1990, 61 (06) :953-963
[10]
In vitro tracking of IL-7 responsiveness and gene expression during commitment of bipotent B-cell/macrophage progenitors [J].
Kee, BL ;
Paige, CJ .
CURRENT BIOLOGY, 1996, 6 (09) :1159-1169