Xu Jian, Zheng Shu-sen, Liang Ting-bo, Xie Hai-yang, Shen Ke-zhen, Feng Xiao-wen, Jin Wen-jia
Key Lab of Combined Multi-Organ Transplantation, Ministry of Health, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Zhonghua Yi Xue Za Zhi. 2005 May 18;85(18):1238-42.
To evaluate the effect of ciclosporin A (CsA) on the organogenesis and function of embryonic metanephroi allografted into adult rats.
The whole metanephroi from the 15, 16 and 17 embryonic day-old (E15, E16, E17) embryos of Sprague-Dawley (SD) rat were allografted into the omenta of SD adult rats with their left kidneys resected, which were divided into 2 categories: 3 CsA-treated groups of 10 rats (E15CsASD, E16CsASD, and E17CsASD) and 3 non-CsA-treated groups of 10 rats (E15SD, E16SD, and E17SD). Thirty SD rats without kidney resection were divided into 6 equal groups and underwent allografting embryonic metanephroi in the same manner as mentioned above. The E15 metanephroi of Lewis rats were allografted into the omenta of Thirty adult Brown Norway (BN) rats with one kidney resected. Were divided into 6 equal groups, received allografting of embryonic metanephroi, and injected with CsA of normal saline in the manner as mentioned above (E15CsABN and E15BN). Two to 4 weeks after implantation, the metanephroi allografted in host rats were removed for histopathological examination or anastomosed for renal function measurement 4 weeks later.
(1) Four weeks after implantation, the E17SD and E16SD metanephroi showed signs of acute rejection as hypercellular glomeruli and mononuclear cell infiltration in the interstitium. The E16CsASD and E17CsASD metanephroi formed mature nephrons and collecting ducts with few lymphocytic infiltrates. After CsA was discontinued, the E16CsASD and E17CsASD metanephroi were rejected fully within 21 days. (2) 4 weeks after implantation, the E15SD metanephroi were enlarged, became vascularized, and developed mature tubules and glomeruli; however, they were rejected by 100 days after implantation. The E15 Lewis metanephroi were fully rejected within two weeks in the BN adult rats. With CsA administrated, the E15 Lewis metanephroi developed normal mature nephrons and collecting ducts within the adult BN rats. If CsA was discontinued, the E15CsABN metanephroi were rejected. (3) The E15CsASD metanephroi had significantly lower values of wet weight (P = 0.006) and higher values of creatinine clearances (P = 0.007) than the E15SD metanephros transplants, but were identical to those of the E16CsASD metanephroi (P = 0.948, P = 0.840). (4) The metanephroi did not grow or differentiate in the rats without host kidney resection.
(1) Cyclosporin A may suppress graft rejection, thus normalizing the growth and function of fetal metanephroi in the omenta of host rats. (2) A variety of factors affect the growth and development of allografted metanephroi, whereas rejection remains the major one.
评估环孢素A(CsA)对移植到成年大鼠体内的胚胎后肾器官发生及功能的影响。
将15、16和17日龄(E15、E16、E17)的Sprague-Dawley(SD)大鼠胚胎的完整后肾移植到左肾已切除的成年SD大鼠大网膜内,分为2类:3个CsA处理组,每组10只大鼠(E15CsASD、E16CsASD和E17CsASD);3个非CsA处理组,每组10只大鼠(E15SD、E16SD和E17SD)。30只未切除肾脏的SD大鼠分为6个相等的组,以与上述相同的方式进行胚胎后肾移植。将Lewis大鼠的E15后肾移植到30只切除一侧肾脏的成年Brown Norway(BN)大鼠大网膜内。分为6个相等的组,进行胚胎后肾移植,并按上述方式注射CsA或生理盐水(E15CsABN和E15BN)。植入后2至4周,取出宿主大鼠体内移植的后肾进行组织病理学检查,或在4周后吻合以测量肾功能。
(1)植入后4周,E17SD和E16SD后肾出现急性排斥反应迹象,表现为肾小球细胞增多和间质单核细胞浸润。E16CsASD和E17CsASD后肾形成成熟的肾单位和集合管,淋巴细胞浸润较少。停用CsA后,E16CsASD和E17CsASD后肾在21天内被完全排斥。(2)植入后4周,E15SD后肾增大、血管化,并发育出成熟的肾小管和肾小球;然而,它们在植入后100天被排斥。E15 Lewis后肾在成年BN大鼠中两周内被完全排斥。给予CsA后,成年BN大鼠体内的E15 Lewis后肾发育出正常成熟的肾单位和集合管。停用CsA后,E15CsABN后肾被排斥。(3)E15CsASD后肾的湿重显著低于E15SD后肾移植组(P = 0.006),肌酐清除率高于E15SD后肾移植组(P = 0.007),但与E16CsASD后肾相同(P = 0.948,P = 0.840)。(4)在未切除宿主肾脏的大鼠中,后肾未生长或分化。
(1)环孢素A可抑制移植排斥反应,从而使宿主大鼠大网膜内胎儿后肾的生长和功能正常化。(2)多种因素影响移植后肾的生长发育,而排斥反应仍是主要因素。