Adoptive transfer of nuclear factor-κB-inactive macrophages to the glomerulus

Background. Macrophages have been regarded as "blackguards" in the generation of glomerular injury. However, it is still unclear what kind of cellular machinery is responsible for their pathogenic actions. To explore this issue, this investigation aims at developing a novel strategy using adoptive transfer of "loss-of-function" macrophages to the glomerulus. As a prototypal investigation, this study examines a role for nuclear factor-KB (NF-KB) in effector actions of macrophages within the glomerular microenvironment. Methods. NF-KB-inactive macrophages, NIKMAC(NR), were created by transduction of NR8383 rat macrophages with retrovirus encoding a super-repressor mutant of I kappa B alpha, I kappa B alpha M. The effector functions of NIKMAC(NR) cells on resident cells were evaluated by coculture, cross-feeding, and in vivo macrophage transfer. Results. Rat mesangial cells cocultured with control macrophages showed abundant expression of activation markers, including monocyte chemoattractant protein-1, stromelysin, and gelatinase B. In contrast, coculture with NIKMAC(NR) macrophages induced only modest gene expression. Similarly, culture medium conditioned by activated, control macrophages triggered mesangial cells and isolated glomeruli to express the activation markers, whereas the stimulatory effect was not observed in medium conditioned by NIKMAC(NR) macrophages. To evaluate effector actions of NIKMAC(NR) macrophages in the glomerulus, control macrophages and NIKMAC(NR) cells were transferred into normal rat glomeruli via renal artery injection. After the transfer of control macrophages, substantial induction of the activation marker stromelysin was observed in resident glomerular cells. This induction was dramatically diminished in the glomeruli transferred with NIKMAC(NR) macrophages. Conclusions. Inactivation of NF-KB in macrophages effectively disrupted paracrine, stimulatory loops from macrophages to resident glomerular cells. A combination of "loss-of-function" strategies with the technique for adoptive cell transfer is thus useful to explore pathophysiologic roles for certain machinery of macrophages within the glomerulus.