将基因工程细胞转移到肾小球。

M Kitamura
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引用次数: 2

摘要

在大鼠中,注入肾循环的培养细胞被困在肾小球中。这种特殊的特性允许产生嵌合肾小球,其中填充了基因工程细胞。利用体外工程改造的肾小球细胞,可以产生产生重组基因产物的肾小球。这种方法将有助于确定肾小球中某种基因产物的局部功能,并有助于肾小球疾病的治疗干预。活化白细胞向肾小球的转移有助于阐明浸润细胞对肾小球结构和功能的病理作用。使用某些基因功能被选择性增强或删除的白细胞,应该能够揭示白细胞相关基因在肾小球病理生理中的确切作用。工程白细胞的转移也允许研究在正常和病理情况下驻留细胞如何调节浸润细胞的活性。本文总结了目前工程细胞过继转移到肾小球的经验,并讨论了其在肾脏研究中的潜在应用。
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Transfer of genetically engineered cells to the glomerulus.

In the rat, cultured cells injected into the renal circulation are entrapped in the glomerulus. This peculiar property allows to create chimeric glomeruli in which genetically engineered cells are populated. Using glomerular cells engineered in vitro, it is feasible to generate glomeruli that produce recombinant gene products. This approach would be useful for identification of local function of a certain gene product in the glomerulus and for therapeutic intervention in glomerular disease. Transfer of activated leukocytes to the glomerulus is useful to elucidate pathologic actions of infiltrating cells on the glomerular structure and function. Use of leukocytes in which certain gene function is selectively reinforced or deleted should enable to disclose exact roles of leukocyte-associated genes in glomerular pathophysiology. Transfer of engineered leukocytes also allows to investigate how resident cells modulate the activity of infiltrating cells in normal and pathologic circumstances. This article summarizes current experience with adoptive transfer of engineered cells to the glomerulus and addresses its potential application to kidney research.

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