Hematopoietic origin of hepatic stellate cells in the adult liver.

@article{citeulike:2799306, abstract = {Hepatic stellate cells are believed to play a key role in the development of liver fibrosis. Several studies have reported that bone marrow cells can give rise to hepatic stellate cells. We hypothesized that hepatic stellate cells are derived from hematopoietic stem cells. To test this hypothesis, we generated chimeric mice by transplantation of clonal populations of cells derived from single enhanced green fluorescent protein (EGFP)-marked Lin(-)Sca-1(+)c-kit(+)CD34(-) cells and examined the histology of liver tissues obtained from the chimeric mice with carbon tetrachloride (CCl(4))-induced injury. After 12 weeks of CCl(4) treatment, we detected EGFP(+) cells in the liver, and some cells contained intracytoplasmic lipid droplets. Immunofluorescence analysis demonstrated that 50\% to 60\% of the EGFP(+) cells were negative for CD45 and positive for vimentin, glial fibrillary acidic protein, ADAMTS13, and alpha-smooth muscle actin. Moreover, EGFP(+) cells isolated from the liver synthesized collagen I in culture. These phenotypes were consistent with those of hepatic stellate cells. The hematopoietic stem cell-derived hepatic stellate cells seen in male-to-male transplants revealed only one Y chromosome. Our findings suggest that hematopoietic stem cells contribute to the generation of hepatic stellate cells after liver injury and that the process does not involve cell fusion.}, address = {Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Mie, Japan.}, author = {Miyata, E. and Masuya, M. and Yoshida, S. and Nakamura, S. and Kato, K. and Sugimoto, Y. and Shibasaki, T. and Yamamura, K. and Ohishi, K. and Nishii, K. and Ishikawa, F. and Shiku, H. and Katayama, N. }, citeulike-article-id = {2799306}, doi = {10.1182/blood-2007-07-101261}, issn = {0006-4971}, journal = {Blood}, month = {February}, number = {4}, pages = {2427--2435}, posted-at = {2008-05-14 16:39:29}, priority = {2}, title = {Hematopoietic origin of hepatic stellate cells in the adult liver.}, url = {http://dx.doi.org/10.1182/blood-2007-07-101261}, volume = {111}, year = {2008} }

TY - JOUR ID - citeulike:2799306 L3 - citeulike-article-id:2799306 TI - Hematopoietic origin of hepatic stellate cells in the adult liver. JF - Blood VL - 111 IS - 4 SP - 2427 EP - 2435 AD - Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Mie, Japan. SN - 0006-4971 N2 - Hepatic stellate cells are believed to play a key role in the development of liver fibrosis. Several studies have reported that bone marrow cells can give rise to hepatic stellate cells. We hypothesized that hepatic stellate cells are derived from hematopoietic stem cells. To test this hypothesis, we generated chimeric mice by transplantation of clonal populations of cells derived from single enhanced green fluorescent protein (EGFP)-marked Lin(-)Sca-1(+)c-kit(+)CD34(-) cells and examined the histology of liver tissues obtained from the chimeric mice with carbon tetrachloride (CCl(4))-induced injury. After 12 weeks of CCl(4) treatment, we detected EGFP(+) cells in the liver, and some cells contained intracytoplasmic lipid droplets. Immunofluorescence analysis demonstrated that 50% to 60% of the EGFP(+) cells were negative for CD45 and positive for vimentin, glial fibrillary acidic protein, ADAMTS13, and alpha-smooth muscle actin. Moreover, EGFP(+) cells isolated from the liver synthesized collagen I in culture. These phenotypes were consistent with those of hepatic stellate cells. The hematopoietic stem cell-derived hepatic stellate cells seen in male-to-male transplants revealed only one Y chromosome. Our findings suggest that hematopoietic stem cells contribute to the generation of hepatic stellate cells after liver injury and that the process does not involve cell fusion. AU - Miyata, E AU - Masuya, M AU - Yoshida, S AU - Nakamura, S AU - Kato, K AU - Sugimoto, Y AU - Shibasaki, T AU - Yamamura, K AU - Ohishi, K AU - Nishii, K AU - Ishikawa, F AU - Shiku, H AU - Katayama, N PY - 2008/02/15/ UR - http://dx.doi.org/10.1182/blood-2007-07-101261 ER -