Rhodes J A, Fitzgibbon D H, Macchiarulo P A, Murphy R A
Dev Biol. 1987 May;121(1):247-52. doi: 10.1016/0012-1606(87)90156-4.
Epidermal growth factor (EGF) causes precocious eruption of incisors in vivo and is mitogenic for tooth-derived cells in vitro. These two observations lead to the hypothesis that the EGF-induced precocious eruption is the result of an increase in the size of the incisor. To test this hypothesis, neonatal mice were injected daily with various doses of EGF and, seven days after birth, were perfused with fixative. EGF causes a retardation of overall growth (as measured by body weight) and a dose-dependent thickening of the epidermis. The incisors were examined in midsagittal histological sections and in X-ray microradiographs. Contrary to our expectations, EGF causes a dose-dependent decrease in the size of the incisors. This result suggests that the stimulation of the growth of odontogenic cells seen in tissue culture is not part of the physiological response to EGF in vivo and that EGF-induced precocious eruption of incisors is not due to an increase in the growth rate of the tooth.
表皮生长因子(EGF)在体内可导致门牙过早萌出,在体外对牙齿来源的细胞具有促有丝分裂作用。这两个观察结果引出一个假设,即EGF诱导的过早萌出是门牙尺寸增加的结果。为了验证这一假设,每天给新生小鼠注射不同剂量的EGF,并在出生七天后用固定剂进行灌注。EGF会导致整体生长迟缓(通过体重衡量)以及表皮呈剂量依赖性增厚。在矢状面组织学切片和X射线显微放射照片中检查门牙。与我们的预期相反,EGF会导致门牙尺寸呈剂量依赖性减小。这一结果表明,在组织培养中观察到的对牙源性细胞生长的刺激并非EGF在体内生理反应的一部分,并且EGF诱导的门牙过早萌出并非由于牙齿生长速率的增加。