Phospholipase C-γ1 (PLC-γ1) is involved in a variety of intracellular signaling via many growth factor receptors and T-cell receptor. To explore the role of PLC-γ1 in vivo, we generated the PLC-γ1-deficient (plc-γ1–/–) mice, which died of growth retardation at embryonic day 8.5-9.5 in utero. Therefore, we examined plc-γ1–/– chimeric mice generated with plc-γ1–/– embryonic stem (ES) cells for further study. Pathologically, plc-γ1–/– chimeras showed multicystic kidney due to severe renal dysplasia and renal tube dilation. Flow cytometric analysis and glucose phosphate isomerase assay revealed very few hematopoietic cells derived from the plc-γ1–/– ES cells in the mutant chimeras. However, differentiation of plc-γ1–/– ES cells into erythrocytes and monocytes/macrophages in vitro was observed to a lesser extent compared with control wild-type ES cells. These data suggest that PLC-γ1 plays an essential role in the renal development and hematopoiesis in vivo.
Deficiency of phospholipase C-γ1 impairs renal development and hematopoiesis
Masatoshi Shirane, Hirofumi Sawa, Yoshiyasu Kobayashi, Toru Nakano, Kenji Kitajima, Yoichi Shinkai, Kazuo Nagashima, Izumi Negishi; Deficiency of phospholipase C-γ1 impairs renal development and hematopoiesis. Development 15 December 2001; 128 (24): 5173–5180. doi: https://doi.org/10.1242/dev.128.24.5173
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