Kawase T, Suzuki A
Department of Pharmacology, Niigata University School of Dentistry, Japan.
Bone Miner. 1990 Jul;10(1):61-70. doi: 10.1016/0169-6009(90)90049-l.
A number of studies have shown membrane phospholipid metabolism to have an important role in biological mineralization. We considered the effects of exogenously applied phosphatidic acid (PA), a minor component of membrane phospholipids, on an osteoblast-like cell line, MOB 3-4. Exogenous PA (10-40 micrograms/ml) raised the level of cytoplasmic free Ca2+ [( Ca2+]i), independent of the level of extracellular Ca2+, in a dose-dependent fashion, and this Ca2+ response to PA gradually fell on serial application of PA. In a dose-dependent manner, exogenous PA also increased inositol 1,4,5-trisphosphate (IP3) accumulation and cytoplasmic pH, but decreased basal cAMP level. This cytoplasmic alkalinization was inhibited by pretreatment with nonspecific protein kinase C (PKC) inhibitors, such as sphingosine or H-7. A long-term incubation with PA increased alkaline phosphatase (ALP) activity and cell proliferation. Exogenous PA thus appeared to increase IP3 accumulation by activating phospholipase C, raise [Ca2+] by releasing Ca2+ from intracellular stores, induce cytoplasmic alkalinization via a PKC-dependent mechanism, and simultaneously decrease basal cAMP level. We suggest that these initial responses may be responsible for the increase in ALP activity and the proliferation of PA-treated MOB 3-4 cells.
多项研究表明,膜磷脂代谢在生物矿化过程中发挥着重要作用。我们研究了外源性添加的磷脂酸(PA,膜磷脂的一种次要成分)对成骨样细胞系MOB 3-4的影响。外源性PA(10 - 40微克/毫升)以剂量依赖的方式提高了细胞质游离Ca2+([Ca2+]i)的水平,且与细胞外Ca2+水平无关,并且在连续添加PA后,这种对PA的Ca2+反应逐渐下降。外源性PA还以剂量依赖的方式增加了肌醇1,4,5-三磷酸(IP3)的积累和细胞质pH值,但降低了基础cAMP水平。这种细胞质碱化被非特异性蛋白激酶C(PKC)抑制剂(如鞘氨醇或H-7)预处理所抑制。长期用PA孵育会增加碱性磷酸酶(ALP)活性和细胞增殖。因此,外源性PA似乎通过激活磷脂酶C来增加IP3积累,通过从细胞内储存中释放Ca2+来提高[Ca2+],通过PKC依赖的机制诱导细胞质碱化,同时降低基础cAMP水平。我们认为,这些初始反应可能是PA处理的MOB 3-4细胞中ALP活性增加和细胞增殖的原因。