Stimulative effect of somatostatin on cell proliferation in cultured chondrocytes.

Medical biology Pub Date : 1987-01-01
O Johansson, K Madsen
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Abstract

We have earlier demonstrated that human growth hormone stimulates DNA synthesis and proteoglycan production in cultured chondrocytes. The present study is concerned with the effects of somatostatin and other neuropeptides on cell proliferation by cultured rat rib growth plate chondrocytes. Chondrocytes were isolated from the growth plates by collagenase digestion and cultured as monolayers in multiwell plates. The cells were allowed to attach overnight and subsequently incubated for 24 h under serum-free conditions to establish growth arrest. Somatostatin and other peptides were then added and the cultures were incubated for 18 h. Finally, the cultures were labelled for 6 h with tritiated thymidine in the presence of peptide. For screening purposes, the effect on DNA-synthesis was assayed as incorporation of [3H]-thymidine into acid-insoluble material. For a more exact estimate, parallel cultures were prepared for autoradiography and the fraction of labelled nuclei was determined by counting. Among the peptides we tested (somatostatin, GRF, TRH, SP, mENK, PHI, VIP, hCT) only somatostatin had any discernible effect on DNA synthesis, with an apparently optimal effect at 10 fM. This concentration is well within the range found in various tissues in vivo and suggests a physiological role for somatostatin in chondrocyte growth regulation. Further experiments are required, however, to clarify by which mechanism somatostatin influences the cells and whether the peptide interacts with other growth factors such as the IGFs.

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生长抑素对培养软骨细胞增殖的促进作用。
我们早先已经证明,人类生长激素刺激DNA合成和蛋白多糖的生产在培养软骨细胞。本研究探讨生长抑素等神经肽对培养大鼠肋生长板软骨细胞增殖的影响。用胶原酶消化法从生长板中分离软骨细胞,在多孔板中培养成单层软骨细胞。让细胞贴壁过夜,随后在无血清条件下培养24小时以建立生长抑制。然后加入生长抑素和其他多肽,培养18小时。最后,在多肽存在的情况下,用氚化胸腺嘧啶标记6小时。为了筛选目的,将[3H]-胸腺嘧啶掺入酸不溶性物质中,测定了对dna合成的影响。为了更准确的估计,平行培养准备放射自显影和标记核的比例是通过计数来确定的。在我们测试的肽(生长抑素,GRF, TRH, SP, mENK, PHI, VIP, hCT)中,只有生长抑素对DNA合成有明显的影响,在10 fM时效果最佳。这个浓度在体内各种组织中发现的范围内,表明生长抑素在软骨细胞生长调节中的生理作用。然而,需要进一步的实验来阐明生长抑素影响细胞的机制,以及该肽是否与其他生长因子(如igf)相互作用。
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