AMEBOID MICROGLIA EXPRESSING G(D3) GANGLIOSIDE ARE CONCENTRATED IN REGIONS OF OLIGODENDROGENESIS DURING DEVELOPMENT OF THE RAT CORPUS-CALLOSUM

被引:35
作者
ELLISON, JA
DEVELLIS, J
机构
[1] UNIV CALIF LOS ANGELES, SCH MED,DEPT ANAT & CELL BIOL, MENTAL RETARDAT RES CTR,BRAIN RES INST, LOS ANGELES, CA 90024 USA
[2] UNIV CALIF LOS ANGELES, SCH MED,DEPT PSYCHIAT,MENTAL RETARDAT RES CTR, BRAIN RES INST,STRUCT BIO, LOS ANGELES, CA 90024 USA
关键词
GLIAL DEVELOPMENT; PHAGOCYTOSIS; PDGF RECEPTOR; ED1;
D O I
10.1002/glia.440140207
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In a recent study we demonstrated expression of the platelet-derived growth factor or receptor (PDGFR alpha) in cells of the early oligodendrocyte lineage that were identified as either G(D3) ganglioside+ oligodendrocyte progenitors or O4 sulfatide+ preoligodendrocytes. We also identified a subpopulation of G(D3) immunoreactive cells that did not express mRNA for the PDGF receptor. The distinct large amoeboid morphology of these cells was characteristic of cells in the macrophage lineage rather than in the oligodendrocyte lineage. To determine if the G(D3)-positive but PDGFR alpha mRNA-negative cells were in the macrophage lineage, we compared the spatial and temporal expression patterns of G(D3) ganglioside and ED1, a macrophage-specific antigen. Analysis prenatally indicated that at embryonic day 15, ED1+ and G(D3)+ cell populations resided in the subpial connective tissue. At embryonic day 21, these two populations were seen in a region extending from the lateral ventricle through the subventricular and intermediate zones. In this study we report that these large, round, G(D3) immunoreactive cells have the same cell morphology and anatomical distribution as the ED1 immunoreactive cells. Both cell populations contained pyknotic nuclei within their cytoplasm. Furthermore, the G(D3)+/PDGFR alpha- cells appear to be involved in clearing cellular debris in regions of gliogenesis. These data suggest that this subpopulation of G(D3) immunoreactive cells belongs to the microglia/macrophage lineage. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:123 / 132
页数:10
相关论文
共 32 条
[1]   CELL-DEATH AND CONTROL OF CELL-SURVIVAL IN THE OLIGODENDROCYTE LINEAGE [J].
BARRES, BA ;
HART, IK ;
COLES, HSR ;
BURNE, JF ;
VOYYODIC, JT ;
RICHARDSON, WD ;
RAFF, MC .
CELL, 1992, 70 (01) :31-46
[2]  
CHUGANI DC, 1991, J NEUROSCI, V11, P256
[3]  
DIJKSTRA CD, 1985, IMMUNOLOGY, V54, P589
[4]   CELL-SURFACE ANTIGENS OF HUMAN-MALIGNANT MELANOMA - DEFINITION OF 6 ANTIGENIC SYSTEMS WITH MOUSE MONOCLONAL-ANTIBODIES [J].
DIPPOLD, WG ;
LLOYD, KO ;
LI, LTC ;
IKEDA, H ;
OETTGEN, HF ;
OLD, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (10) :6114-6118
[5]   PLATELET-DERIVED GROWTH-FACTOR RECEPTOR IS EXPRESSED BY CELLS IN THE EARLY OLIGODENDROCYTE LINEAGE [J].
ELLISON, JA ;
DEVELLIS, J .
JOURNAL OF NEUROSCIENCE RESEARCH, 1994, 37 (01) :116-128
[6]   NASCENT MICROGLIA IN THE DEVELOPING BRAIN [J].
FERRER, I ;
SARMIENTO, J .
ACTA NEUROPATHOLOGICA, 1980, 50 (01) :61-67
[7]   THE MORPHOLOGY AND PHASED OUTGROWTH OF CALLOSAL AXONS IN THE FETAL-RAT [J].
FLOETER, MK ;
JONES, EG .
DEVELOPMENTAL BRAIN RESEARCH, 1985, 22 (01) :7-18
[8]   GD3 GANGLIOSIDE IS A GLYCOLIPID CHARACTERISTIC OF IMMATURE NEUROECTODERMAL CELLS [J].
GOLDMAN, JE ;
HIRANO, M ;
YU, RK ;
SEYFRIED, TN .
JOURNAL OF NEUROIMMUNOLOGY, 1984, 7 (2-3) :179-192
[9]   NEW EXPRESSION OF MYELOMONOCYTIC ANTIGENS BY MICROGLIA AND PERIVASCULAR CELLS FOLLOWING LETHAL MOTOR-NEURON INJURY [J].
GRAEBER, MB ;
STREIT, WJ ;
KIEFER, R ;
SCHOEN, SW ;
KREUTZBERG, GW .
JOURNAL OF NEUROIMMUNOLOGY, 1990, 27 (2-3) :121-132
[10]   STIMULATION OF IN-VITRO MYELIN SYNTHESIS BY MICROGLIA [J].
HAMILTON, SP ;
ROME, LH .
GLIA, 1994, 11 (04) :326-335