Immunohistochemical evidence for a mesothelial contribution to the ventral wall of the avian aorta

被引:16
作者
Pérez-Pomares, JM [1 ]
Macías-López, D [1 ]
García-Garrido, L [1 ]
Muñoz-Chápuli, R [1 ]
机构
[1] Univ Malaga, Fac Ciencias, Dept Biol Anim, E-29071 Malaga, Spain
来源
HISTOCHEMICAL JOURNAL | 1999年 / 31卷 / 12期
关键词
D O I
10.1023/A:1003997919311
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We report morphological and immunohistochemical evidence for a translocation of cells from the coelomic mesothelium to the aortic wall between the developmental stages HH16 and HH22 of the quail embryos. The coelomic mesothelial cells closest to the aorta showed, at these stages, increased mitotic activity, reduced intercellular adhesion, loss of tight junctions, and long basal cytoplasmic processes. Coinciding with these morphological traits, cytokeratin immunoreactivity was found in the mesothelium, in cells of the aortic wall and throughout the ventral periaortic mesenchyme (but not in the lateral and dorsal aortic regions). Vimentin immunoreactivity colocalized with cytokeratin in the mesothelial cells adjacent to the aorta. In the ventral aortic wall, cytokeratin colocalized with smooth muscle alpha-actin and with the 1E12 antigen (a smooth muscle-specific alpha-actinin isoform). We think that the morphological and immunolocalization data observed are compatible with an epithelial-mesenchymal transition by which mesothelial-derived cells contribute to the splanchnic mesoderm and aortic wall. The precise coincidence between the mesothelial contribution and the emergence of the aortic smooth muscle cells progenitors, as well as the immunolocalization data, suggest a potential relationship of the mesothelial-derived cells with this cell lineage. This may explain the observed ventrodorsal asymmetry in the distribution of smooth muscle cells progenitors in the aortic wall.
引用
收藏
页码:771 / 779
页数:9
相关论文
共 26 条
[1]  
CORMIER F, 1988, DEVELOPMENT, V102, P279
[2]   Embryonic endothelial cells transdifferentiate into mesenchymal cells expressing smooth muscle actins in vivo and in vitro [J].
DeRuiter, MC ;
Poelmann, RE ;
VanMunsteren, JC ;
Mironov, V ;
Markwald, RR ;
GittenbergerdeGroot, AC .
CIRCULATION RESEARCH, 1997, 80 (04) :444-451
[3]   Common epicardial origin of coronary vascular smooth muscle, perivascular fibroblasts, and intermyocardial fibroblasts in the avian heart [J].
Dettman, RW ;
Denetclaw, W ;
Ordahl, CP ;
Bristow, J .
DEVELOPMENTAL BIOLOGY, 1998, 193 (02) :169-181
[4]   DIFFUSE INTRAEMBRYONIC HEMATOPOIESIS IN NORMAL AND CHIMERIC AVIAN DEVELOPMENT [J].
DIETERLENLIEVRE, F ;
MARTIN, C .
DEVELOPMENTAL BIOLOGY, 1981, 88 (01) :180-191
[5]   MEDIAL EDGE EPITHELIUM TRANSFORMS TO MESENCHYME AFTER EMBRYONIC PALATAL SHELVES FUSE [J].
FITCHETT, JE ;
HAY, ED .
DEVELOPMENTAL BIOLOGY, 1989, 131 (02) :455-474
[6]   FORMATION OF CYTOSKELETAL ELEMENTS DURING MOUSE EMBRYOGENESIS .3. PRIMARY MESENCHYMAL CELLS AND THE 1ST APPEARANCE OF VIMENTIN FILAMENTS [J].
FRANKE, WW ;
GRUND, C ;
KUHN, C ;
JACKSON, BW ;
ILLMENSEE, K .
DIFFERENTIATION, 1982, 23 (01) :43-59
[7]   A SERIES OF NORMAL STAGES IN THE DEVELOPMENT OF THE CHICK EMBRYO [J].
HAMBURGER, V ;
HAMILTON, HL .
JOURNAL OF MORPHOLOGY, 1951, 88 (01) :49-&
[8]  
Hay E.D., 1990, Seminars in Developmental Biology, V1, P347
[9]  
Hay ED, 1995, ACTA ANAT, V154, P8
[10]   Development of the aortic vessel wall as defined by vascular smooth muscle and extracellular matrix markers [J].
Hungerford, JE ;
Owens, GK ;
Argraves, WS ;
Little, CD .
DEVELOPMENTAL BIOLOGY, 1996, 178 (02) :375-392