Ballabriga J, Pozas E, Planas A M, Ferrer I
Unitat de Neuropatología, Hospital Princeps d'Espanya, Universitat de Barcelona, Spain.
Brain Res. 1997 Mar 28;752(1-2):315-8. doi: 10.1016/s0006-8993(96)01308-x.
Strong bFGF immunoreactivity was observed in reactive astrocytes, as shown by double-labeling immunohistochemistry of bFGF and GFAP, from days 7 up to 30 (last time point examined) following kainic acid (KA) injection at convulsant doses in the adult rat. bFGF was not found in OX-42-positive reactive microglia. A few reactive glia co-localized FGFR-3 and GFAP, whereas the majority of cells expressing FGFR-3 were OX-42-immunoreactive. This was further supported by the observation that only approximately 10% of reactive glia co-localized bFGF and FGFR-3. These results show that reactive astrocytes are a major source of bFGF during the subacute stages of tissue damage following KA injection and that reactive astrocytes and, most particularly, reactive microglia are putative targets of bFGF through FGFR-3.
在成年大鼠以惊厥剂量注射海藻酸(KA)后的第7天至30天(检查的最后时间点),通过bFGF和GFAP的双重免疫组化显示,在反应性星形胶质细胞中观察到强烈的bFGF免疫反应性。在OX-42阳性反应性小胶质细胞中未发现bFGF。少数反应性胶质细胞使FGFR-3和GFAP共定位,而大多数表达FGFR-3的细胞是OX-42免疫反应性的。仅约10%的反应性胶质细胞使bFGF和FGFR-3共定位这一观察结果进一步支持了这一点。这些结果表明,在KA注射后组织损伤的亚急性阶段,反应性星形胶质细胞是bFGF的主要来源,并且反应性星形胶质细胞,尤其是反应性小胶质细胞,是bFGF通过FGFR-3的假定靶标。