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降钙素原氨基末端裂解肽(N-proCT)在体外对正常克隆大鼠成骨细胞和前成骨细胞缺乏生物学活性。

The procalcitonin amino-terminal cleavage peptide (N-proCT) lacks biological activity on normal clonal rat osteoblastic and preosteoblastic cells in vitro.

作者信息

Guenther H L, Fleisch H

机构信息

Department of Pathophysiology, University of Berne, Switzerland.

出版信息

Calcif Tissue Int. 1991 Aug;49(2):138-40. doi: 10.1007/BF02565137.

Abstract

The human-derived procalcitonin amino-terminal cleavage peptide, N-proCT has previously been shown to act mitogenically on isolated chicken and human osteoblast-like cells and on the human osteosarcoma cell line U-2 OS. We have examined the effect of N-proCT on growth and phenotype of cloned rat osteoblastic and preosteoblastic cells. Neither cell growth nor the phenotype (ALP, PTH response) of either cell type was significantly changed by the procalcitonin cleavage peptide.

摘要

人源降钙素原氨基末端裂解肽(N-proCT)先前已被证明对分离的鸡和人成骨细胞样细胞以及人骨肉瘤细胞系U-2 OS具有促有丝分裂作用。我们研究了N-proCT对克隆的大鼠成骨细胞和前成骨细胞生长及表型的影响。降钙素原裂解肽对这两种细胞类型的细胞生长和表型(碱性磷酸酶、甲状旁腺激素反应)均无显著影响。

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