The Utah team used MSC for several reasons, notably the fact that they can be harvested easily from bone marrow, isolated, grown in culture and genetically engineered. To test that MSC subsequently used in these studies retained their phenotype after being cultured, the researchers routinely tested whether their characteristic potential to differentiate into fat and bone cells was preserved.
The researchers conceded that it "is surprising that the very transient presence of MSC in the injured kidney, as we document, is sufficient to greatly ameliorate the course" of I/R ARF and also note that the rat model of ARF used in the study is "a suitable if somewhat imperfect model of the most common and the most treatment-resistant type of human ischemic ARF."
* Current studies are investigating the collective and individual renoprotective capacity of cytokines temporarily released by MSC.
* Two clinical efforts are planned. First will be a compassionate study in Europe next year in patients with complicated bone marrow transplants, a setting where such stem cells already are approved for use. If successful, a compassionate-use study in patients with severe ARF and multiorgan failure will be designed, eventually leading to clinical trials.
* Though no adverse effects were seen in these experiments, long-term studies are needed to prove that no adverse effects occur after in vivo administration of adult MSC.
* Also to be determined is whether
Source:American Physiological Society