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磷酸盐与甲状旁腺激素相关蛋白相互作用,以调节软骨内骨形成。

Phosphate interacts with PTHrP to regulate endochondral bone formation.

作者信息

Liu Eva S, Zalutskaya Alena, Chae Byongsoo Timothy, Zhu Eric D, Gori Francesca, Demay Marie B

机构信息

Division of Endocrinology, Diabetes, and Hypertension (E.S.L.), Brigham and Women's Hospital, Boston, Massachusetts 02115; Endocrine Unit (E.S.L., A.Z., B.T.C., E.D.Z., F.G., M.B.D.), Massachusetts General Hospital, Boston, Massachusetts 02114; Harvard Medical School (E.S.L., A.Z., F.G., M.B.D.), Boston, Massachusetts 02115.

出版信息

Endocrinology. 2014 Oct;155(10):3750-6. doi: 10.1210/en.2014-1315. Epub 2014 Jul 24.

Abstract

Phosphate and parathyroid hormone related peptide (PTHrP) are required for normal growth plate maturation. Hypophosphatemia impairs hypertrophic chondrocyte apoptosis leading to rachitic expansion of the growth plate; however, the effect of phosphate restriction on chondrocyte differentiation during endochondral bone formation has not been examined. Investigations were, therefore, undertaken to address whether phosphate restriction alters the maturation of embryonic d15.5 murine metatarsal elements. Metatarsals cultured in low phosphate media exhibited impaired chondrocyte differentiation, analogous to that seen with PTHrP-treatment of metatarsals cultured in control media. Because phosphate restriction acutely increases PTHrP expression in cultured metatarsals, studies were undertaken to determine if this increase in PTHrP plays a pathogenic role in the impaired chondrocyte differentiation observed under low phosphate conditions. In contrast to what was observed with wild-type metatarsal elements, phosphate restriction did not impair the differentiation of metatarsals isolated from PTHrP heterozygous or PTHrP knockout mice. In vivo studies in postnatal mice demonstrated that PTHrP haploinsufficiency also prevents the impaired hypertrophic chondrocyte apoptosis observed with phosphate restriction. To determine how signaling through the PTH/PTHrP receptor antagonizes the pro-apoptotic effects of phosphate, investigations were performed in primary murine hypertrophic chondrocytes. Receptor activation impaired phosphate-induced Erk1/2 phosphorylation specifically in the mitochondrial fraction and decreased levels of mitochondrial Bad, while increasing cytosolic phospho-Bad. Thus, these data demonstrate that phosphate restriction attenuates chondrocyte differentiation as well as impairing hypertrophic chondrocyte apoptosis and implicate a functional role for the PTH/PTHrP signaling pathway in the abnormalities in chondrocyte differentiation and hypertrophic chondrocyte apoptosis observed under phosphate restricted conditions.

摘要

正常生长板成熟需要磷酸盐和甲状旁腺激素相关肽(PTHrP)。低磷血症会损害肥大软骨细胞凋亡,导致生长板佝偻病样扩张;然而,在软骨内骨形成过程中,磷酸盐限制对软骨细胞分化的影响尚未得到研究。因此,开展了相关研究,以探讨磷酸盐限制是否会改变胚胎第15.5天小鼠跖骨的成熟过程。在低磷培养基中培养的跖骨表现出软骨细胞分化受损,类似于在对照培养基中培养的跖骨经PTHrP处理后的情况。由于磷酸盐限制会急性增加培养的跖骨中PTHrP的表达,因此开展了研究,以确定PTHrP的这种增加是否在低磷条件下观察到的软骨细胞分化受损中起致病作用。与野生型跖骨元件的观察结果相反,磷酸盐限制并未损害从PTHrP杂合子或PTHrP基因敲除小鼠分离的跖骨的分化。对出生后小鼠的体内研究表明,PTHrP单倍体不足也可防止在磷酸盐限制时观察到的肥大软骨细胞凋亡受损。为了确定通过PTH/PTHrP受体的信号传导如何拮抗磷酸盐的促凋亡作用,在原代小鼠肥大软骨细胞中进行了研究。受体激活特异性地损害了线粒体部分中磷酸盐诱导的Erk1/2磷酸化,并降低了线粒体Bad的水平,同时增加了细胞质磷酸化Bad的水平。因此,这些数据表明,磷酸盐限制会减弱软骨细胞分化,损害肥大软骨细胞凋亡,并暗示PTH/PTHrP信号通路在磷酸盐限制条件下观察到的软骨细胞分化异常和肥大软骨细胞凋亡中起功能性作用。

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