skeleton
|
• CFU-ALP and CFU osteoblasts are increased in pIpC-treated mice compared with controls
• however, the number of CFU fibroblasts is normal
|
|
• in pIpC-treated bone marrow macrophages
|
|
• osteoblasts from the long bones of pIpC-treated mice exhibit increased ALP activity and formed more mineralized bone nodules compared with control cells
• however, osteoblast proliferation is normal
|
|
• in pIpC-treated mice
|
|
• pIpC-treated mice exhibit reduced resorption pit depths compared with control mice
|
|
• in pIpC-treated mice
|
|
• in pIpC-treated mice
|
|
• in pIpC-treated mice
|
|
• in pIpC-treated mice with reduced trabecular separation
|
|
• in pIpC-treated mice
|
cellular
|
• CFU-ALP and CFU osteoblasts are increased in pIpC-treated mice compared with controls
• however, the number of CFU fibroblasts is normal
|
|
• in pIpC-treated bone marrow macrophages
|
|
• osteoblasts from the long bones of pIpC-treated mice exhibit increased ALP activity and formed more mineralized bone nodules compared with control cells
• however, osteoblast proliferation is normal
|
immune system
|
• in pIpC-treated bone marrow macrophages
|
|
• in pIpC-treated mice
|
|
• pIpC-treated mice exhibit reduced resorption pit depths compared with control mice
|
hematopoietic system
|
• in pIpC-treated bone marrow macrophages
|
|
• in pIpC-treated mice
|
|
• pIpC-treated mice exhibit reduced resorption pit depths compared with control mice
|


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