Gurner A C, Smith J, Cattell V
Am J Pathol. 1987 May;127(2):342-8.
The lineage of Ia antigen expressing (Ia+) cells that have been detected in the parenchyma and interstitium of the rat kidney has not been defined. The authors have studied the origins of Ia+ cells in chimeric rats using monoclonal antibodies to define cells of bone marrow and parenchymal origin. PVGc RTI rats (recipients) received intravenously 2 X 10(6) bone marrow cells from F1 hybrid PVG RTIc/RTIu rats (donors) 1 day after 1000 rads whole body irradiation. Ia chimerism was monitored in blood and isolated glomeruli by immunofluorescence and in frozen sections by immunoperoxidase, using monoclonal antibodies MRC OX3 (anti-Ia RTIu), MRC OX4 (anti-RTIc and u), and MRC OXI (anti-rat leukocyte common antigen). In normal F1 hybrid kidneys, glomerular cell counts were as follows: OXI+, 7.19 +/- 0.23/gl; OX4+, 3.03 +/- 0.14; OX3+, 2.34 +/- 0.1 (76% detectable expression of RTIu). OXI+, OX4+, and OX3+ cells were codistributed in cells in the interstitium between renal tubules. Proximal tubules were weakly OX4+, OX3+. In chimeric rats 5 days after irradiation, blood leukocytes, and renal OX1+ and OX4+ cells were depleted; OX3+ cells were not detected; by 4 weeks blood leukocytes were restored to normal numbers, and 85% of Ia+ cells were OX3+. By 6 weeks OXI+ and OX4+ cells were restored in glomeruli and interstitium, with increasing expression of OX3+ cells; at 10 weeks 75% of glomerular Ia+ cells were OX3+ (equivalent to detectable level of OX3+ cells in normal F1 hybrids) and OX1+, OX4+, and OX3+ cells appeared in equivalent numbers in the interstitium. Groups of proximal tubules were OX4+ and OX3-. These results in established bone marrow chimeras show that in the normal rat kidney bone marrow derived leukocytes expressing Ia antigen are present in the glomerulus and interstitium. Ia antigen is also expressed on some proximal tubular cells. There is no evidence for endothelial Ia positivity.
在大鼠肾脏实质和间质中检测到的表达Ia抗原(Ia+)的细胞谱系尚未明确。作者利用单克隆抗体研究了嵌合大鼠中Ia+细胞的起源,以区分骨髓来源和实质来源的细胞。PVGc RTI大鼠(受体)在接受1000拉德全身照射1天后,静脉注射来自F1杂种PVG RTIc/RTIu大鼠(供体)的2×10⁶个骨髓细胞。通过免疫荧光检测血液和分离的肾小球中的Ia嵌合情况,通过免疫过氧化物酶检测冰冻切片中的Ia嵌合情况,使用单克隆抗体MRC OX3(抗Ia RTIu)、MRC OX4(抗RTIc和u)和MRC OXI(抗大鼠白细胞共同抗原)。在正常F1杂种肾脏中,肾小球细胞计数如下:OXI+,7.ġħ +/- 0.23/个肾小球;OX4+,3.03 +/- 0.ġ4;OX3+,2.34 +/- 0.ġ(RTIu的可检测表达率为76%)。OXI+、OX4+和OX3+细胞在肾小管间的间质细胞中共同分布。近端小管弱阳性表达OX4+、OX3+。在照射后5天的嵌合大鼠中,血液白细胞以及肾脏中的OX1+和OX4+细胞减少;未检测到OX3+细胞;到4周时血液白细胞恢复到正常数量,85%的Ia+细胞为OX3+。到6周时,肾小球和间质中的OXI+和OX4+细胞恢复,OX3+细胞表达增加;在10周时,75%的肾小球Ia+细胞为OX3+(相当于正常F1杂种中OX3+细胞的可检测水平),并且OX1+、OX4+和OX3+细胞在间质中数量相当。成群的近端小管为OX4+和OX3-。在已建立的骨髓嵌合体中的这些结果表明,在正常大鼠肾脏中,表达Ia抗原的骨髓来源白细胞存在于肾小球和间质中。Ia抗原也在一些近端小管细胞上表达。没有证据表明内皮细胞Ia呈阳性。