Schulze-Lohoff E, Zanner S, Ogilvie A, Sterzel R B
Medizinische Klinik IV, Universität Erlangen-Nürnberg, Germany.
Hypertension. 1995 Dec;26(6 Pt 1):899-904. doi: 10.1161/01.hyp.26.6.899.
Diadenosine polyphosphates (diadenosine triphosphate, Ap3A; diadenosine tetraphosphate, Ap4A; diadenosine pentaphosphate, Ap5A; diadenosine hexaphosphate, Ap6A) are potent vasoactive molecules stored and released by platelets. We examined whether these dinucleotides might contribute to the glomerular inflammatory response by stimulating the proliferation of mesangial cells. In cultured rat mesangial cells all four tested dinucleotides (10 to 100 mumol/L) significantly stimulated DNA synthesis as measured by [3H]thymidine uptake at 48 hours (x-fold increase compared with unstimulated control cells: Ap3A, 1.5; Ap4A, 1.8; Ap5A, 1.6; Ap6A, 1.6). In combination with the platelet products platelet-derived growth factor, epidermal growth factor, and serotonin, the dinucleotides synergistically increased DNA synthesis. Dinucleotides by themselves increased cell counts by 23% to 43% at day 2 and augmented mesangial cell growth induced by platelet-derived growth factor, epidermal growth factor, and serotonin. Furthermore, dinucleotides (100 mumol/L) rapidly induced a modest increase in expression of the early growth response gene Egr-1 at 30 minutes (x-fold increase over baseline control: Ap3A, 1.9; Ap4A, 2.8; Ap5A, 2.2; Ap6A, 2.1). We found that extracellular Ap4A was metabolized by mesangial cell ectoenzymes to mononucleotides and adenosine, which also have been shown to be mitogenic for mesangial cells. The combination of Ap4A with mononucleotides or adenosine failed to cause additive stimulation of DNA synthesis in mesangial cells. We conclude that diadenosine polyphosphates stimulate proliferation of cultured mesangial cells and augment mesangial cell growth induced by other mitogens released from platelets. Different molecular mechanisms may be involved in dinucleotide-induced mitogenesis of mesangial cells. Direct effects of dinucleotides on cultured mesangial cells. Direct effects of dinucleotides on cultured mesangial cells appear to play a role because dinucleotides rapidly caused activation of Egr-1.(ABSTRACT TRUNCATED AT 250 WORDS)
二腺苷多磷酸(三磷酸二腺苷,Ap3A;四磷酸二腺苷,Ap4A;五磷酸二腺苷,Ap5A;六磷酸二腺苷,Ap6A)是血小板储存并释放的强效血管活性分子。我们研究了这些二核苷酸是否可能通过刺激系膜细胞增殖而促成肾小球炎症反应。在培养的大鼠系膜细胞中,所有四种受试二核苷酸(10至100 μmol/L)均显著刺激DNA合成,48小时时通过[3H]胸腺嘧啶核苷摄取量来测定(与未刺激的对照细胞相比增加的倍数:Ap3A为1.5;Ap4A为1.8;Ap5A为1.6;Ap6A为1.6)。与血小板产物血小板衍生生长因子、表皮生长因子和5-羟色胺联合时,这些二核苷酸协同增加DNA合成。二核苷酸自身在第2天使细胞计数增加23%至43%,并增强了由血小板衍生生长因子、表皮生长因子和5-羟色胺诱导的系膜细胞生长。此外,二核苷酸(100 μmol/L)在30分钟时迅速诱导早期生长反应基因Egr-1的表达适度增加(相对于基线对照增加的倍数:Ap3A为1.9;Ap4A为2.8;Ap5A为2.2;Ap6A为2.1)。我们发现细胞外Ap4A被系膜细胞外酶代谢为单核苷酸和腺苷,它们也已被证明对系膜细胞有促有丝分裂作用。Ap4A与单核苷酸或腺苷的组合未能对系膜细胞的DNA合成产生相加刺激作用。我们得出结论,二腺苷多磷酸刺激培养的系膜细胞增殖,并增强由血小板释放的其他有丝分裂原诱导的系膜细胞生长。不同的分子机制可能参与二核苷酸诱导的系膜细胞有丝分裂。二核苷酸对培养的系膜细胞的直接作用。二核苷酸对培养的系膜细胞的直接作用似乎起作用,因为二核苷酸迅速导致Egr-1激活。(摘要截短于250字)