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花生四烯酸的动员在有丝分裂过程中受到抑制:胞质磷脂酶A2激活的作用。

Arachidonic acid mobilization is suppressed during mitosis: role of cytosolic phospholipase A2 activation.

作者信息

Berlin R D, Preston S F

机构信息

Department of Physiology, University of Connecticut Health Center, Farmington, USA.

出版信息

Biochem J. 1995 Jul 1;309 ( Pt 1)(Pt 1):91-7. doi: 10.1042/bj3090091.

Abstract

In interphase HeLa cells, incubation with histamine or thapsigargin led to the rapid release of arachidonic acid. The release was absolutely dependent on Ca2+, consistent with the activation of an 85 kDa cytosolic phospholipase A2 (cPLA2). In metaphase-arrested HeLa cells, by contrast, the stimulation of arachidonate release by these agents was inhibited by more than 90%. The lack of arachidonic acid release by mitotic cells was at least partly expected, since histamine- or thapsigargin-induced Ca2+ influx and elevations of cytosolic free Ca2+ are known to be strongly inhibited during mitosis [Preston, Sha'afi and Berlin (1991) Cell Regul. 2, 915-925]. Indeed, incubation of interphase cells with the Ca2+ ionophore A23187 alone induced a high level of arachidonate release. However, even A23187 failed to elicit release from mitotic cells. Since the Ca(2+)-dependent release of arachidonate by many cell types is promoted by preincubation with ligands that activate receptors of the tyrosine kinase class, and tumour promoters that lead to the phosphorylation of cPLA2, we determined if the responses of mitotic HeLa cells could be modified by this 'priming' process. We first established that epidermal growth factor and phorbol 12-myristate 13-acetate were effective priming agents in interphase cells: cells preincubated with the hormone or tumour promoter showed a 2-fold stimulation of thapsigargin- or A23187-induced arachidonic acid release. However, none of the priming agents reversed the lack of mitotic cell response. This refractoriness was not caused by destruction of cPLA2 during mitosis: by Western blotting, cPLA2 of interphase and mitotic cells was shown to be present in comparable amounts. Moreover, cPLA2 activities measured in extracts of interphase and mitotic cells were also comparable. Surprisingly, mitotic cPLA2 appeared to be constitutively phosphorylated in non-hormone-treated (control) cells. The results indicate a novel mechanism of regulation by cPLA2 activity in mitotic cells.

摘要

在间期的HeLa细胞中,用组胺或毒胡萝卜素孵育会导致花生四烯酸的快速释放。这种释放绝对依赖于Ca2+,这与一种85 kDa的胞质磷脂酶A2(cPLA2)的激活相一致。相比之下,在中期停滞的HeLa细胞中,这些试剂对花生四烯酸释放的刺激被抑制了90%以上。有丝分裂细胞缺乏花生四烯酸释放至少在一定程度上是可以预期的,因为已知组胺或毒胡萝卜素诱导的Ca2+内流和胞质游离Ca2+的升高在有丝分裂期间会受到强烈抑制[普雷斯顿、沙阿菲和柏林(1991年)《细胞调控》2,915 - 925]。事实上,仅用Ca2+离子载体A23187孵育间期细胞就会诱导高水平的花生四烯酸释放。然而,即使是A23187也无法从有丝分裂细胞中引发释放。由于许多细胞类型中依赖Ca(2+)的花生四烯酸释放会因预先用激活酪氨酸激酶类受体的配体以及导致cPLA2磷酸化的肿瘤促进剂孵育而增强,我们确定有丝分裂的HeLa细胞的反应是否可以通过这种“引发”过程来改变。我们首先确定表皮生长因子和佛波酯12 - 肉豆蔻酸13 - 乙酸酯在间期细胞中是有效的引发剂:用激素或肿瘤促进剂预先孵育的细胞对毒胡萝卜素或A23187诱导的花生四烯酸释放有2倍的刺激作用。然而,没有一种引发剂能逆转有丝分裂细胞反应的缺失。这种难治性不是由有丝分裂期间cPLA2的破坏引起的:通过蛋白质印迹法显示,间期细胞和有丝分裂细胞中的cPLA2含量相当。此外,在间期细胞和有丝分裂细胞提取物中测得的cPLA2活性也相当。令人惊讶的是,在未用激素处理的(对照)细胞中,有丝分裂的cPLA2似乎是组成型磷酸化的。结果表明有丝分裂细胞中cPLA2活性存在一种新的调控机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e21b/1135804/e930c14142a8/biochemj00060-0097-a.jpg

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