Clemens T L, Cormier S, Eichinger A, Endlich K, Fiaschi-Taesch N, Fischer E, Friedman P A, Karaplis A C, Massfelder T, Rossert J, Schlüter K D, Silve C, Stewart A F, Takane K, Helwig J J
Department of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
Br J Pharmacol. 2001 Nov;134(6):1113-36. doi: 10.1038/sj.bjp.0704378.
The cloning of the so-called 'parathyroid hormone-related protein' (PTHrP) in 1987 was the result of a long quest for the factor which, by mimicking the actions of PTH in bone and kidney, is responsible for the hypercalcemic paraneoplastic syndrome, humoral calcemia of malignancy. PTHrP is distinct from PTH in a number of ways. First, PTHrP is the product of a separate gene. Second, with the exception of a short N-terminal region, the structure of PTHrP is not closely related to that of PTH. Third, in contrast to PTH, PTHrP is a paracrine factor expressed throughout the body. Finally, most of the functions of PTHrP have nothing in common with those of PTH. PTHrP is a poly-hormone which comprises a family of distinct peptide hormones arising from post-translational endoproteolytic cleavage of the initial PTHrP translation products. Mature N-terminal, mid-region and C-terminal secretory forms of PTHrP are thus generated, each of them having their own physiologic functions and probably their own receptors. The type 1 PTHrP receptor, binding both PTH(1-34) and PTHrP(1-36), is the only cloned receptor so far. PTHrP is a PTH-like calciotropic hormone, a myorelaxant, a growth factor and a developmental regulatory molecule. The present review reports recent aspects of PTHrP pharmacology and physiology, including: (a) the identification of new peptides and receptors of the PTH/PTHrP system; (b) the recently discovered nuclear functions of PTHrP and the role of PTHrP as an intracrine regulator of cell growth and cell death; (c) the physiological and developmental actions of PTHrP in the cardiovascular and the renal glomerulo-vascular systems; (d) the role of PTHrP as a regulator of pancreatic beta cell growth and functions, and, (e) the interactions of PTHrP and calcium-sensing receptors for the control of the growth of placental trophoblasts. These new advances have contributed to a better understanding of the pathophysiological role of PTHrP, and will help to identify its therapeutic potential in a number of diseases.
1987年所谓的“甲状旁腺激素相关蛋白”(PTHrP)的克隆,是长期寻找一种因子的结果。该因子通过模拟甲状旁腺激素(PTH)在骨骼和肾脏中的作用,导致了高钙血症副肿瘤综合征,即恶性肿瘤体液性高钙血症。PTHrP在许多方面与PTH不同。首先,PTHrP是一个独立基因的产物。其次,除了短的N端区域外,PTHrP的结构与PTH的结构没有密切关系。第三,与PTH相反,PTHrP是一种在全身表达的旁分泌因子。最后,PTHrP的大多数功能与PTH的功能没有共同之处。PTHrP是一种多激素,它由一系列不同的肽激素组成,这些肽激素来自初始PTHrP翻译产物的翻译后内切蛋白水解切割。因此产生了成熟的N端、中间区域和C端分泌形式的PTHrP,它们各自具有自己的生理功能,可能还有自己的受体。1型PTHrP受体既能结合PTH(1 - 34),也能结合PTHrP(1 - 36),是迄今为止唯一克隆的受体。PTHrP是一种类似PTH的钙调节激素、一种肌肉松弛剂、一种生长因子和一种发育调节分子。本综述报告了PTHrP药理学和生理学的最新进展,包括:(a)PTH/PTHrP系统新肽和受体的鉴定;(b)最近发现的PTHrP的核功能以及PTHrP作为细胞生长和细胞死亡的内分泌调节因子的作用;(c)PTHrP在心血管和肾小球血管系统中的生理和发育作用;(d)PTHrP作为胰腺β细胞生长和功能调节因子的作用,以及(e)PTHrP与钙敏感受体在控制胎盘滋养层细胞生长方面的相互作用。这些新进展有助于更好地理解PTHrP的病理生理作用,并将有助于确定其在多种疾病中的治疗潜力。