Kitamura M
Glomerular Bioengineering Unit, Department of Medicine, University College London Medical School, The Rayne Institute, London, UK.
Exp Nephrol. 1999 May-Jun;7(3):259-66. doi: 10.1159/000020611.
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.
在大鼠中,注入肾循环的培养细胞会被困在肾小球中。这种特殊性质使得能够创建嵌合肾小球,其中植入了基因工程细胞。利用体外工程改造的肾小球细胞,生成产生重组基因产物的肾小球是可行的。这种方法对于确定肾小球中特定基因产物的局部功能以及对肾小球疾病进行治疗干预将是有用的。将活化的白细胞转移到肾小球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缺失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学中的确切作用。工程改造白细胞的转移还可以研究驻留细胞在正常和病理情况下如何调节浸润细胞的活性。本文总结了将工程细胞过继转移到肾小球的当前经验,并探讨了其在肾脏研究中的潜在应用。