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正常和蛋白激酶C缺失的瑞士3T3细胞有丝分裂原诱导的钙反应的单细胞分析。

Single-cell analysis of the mitogen-induced calcium responses of normal and protein kinase C-depleted Swiss 3T3 cells.

作者信息

Corps A N, Cheek T R, Moreton R B, Berridge M J, Brown K D

机构信息

Department of Biochemistry, AFRC Institute of Animal Physiology, Cambridge, U.K.

出版信息

Cell Regul. 1989 Nov;1(1):75-86. doi: 10.1091/mbc.1.1.75.

Abstract

Single-cell fluorescence image analysis has been used to characterize the mitogen-induced increases in intracellular free [Ca2+] ([Ca2+]i) in control and protein kinase C-depleted Swiss 3T3 cells. More than 80% of the control cells exhibited fast, transient responses to bombesin, vasopressin, or prostaglandin F2 alpha (PGF2 alpha). In contrast, the [Ca2+]i responses induced by platelet-derived growth factor (PDGF) were markedly more heterogeneous, slower, and often biphasic, with fewer cells (60-70%) responding. The peak [Ca2+]i values obtained in response to each mitogen showed substantial variation between cells. Brief pretreatment of the cells with 12-O-tetradecanoyl phorbol 13-acetate (TPA) reduced the [Ca2+]i responses to bombesin, but did not affect the responses to PDGF. Long-term pretreatment of the cells with TPA to down-modulate protein kinase C resulted in substantially prolonged [Ca2+]i responses to bombesin, vasopressin, and PGF2 alpha, but had no such effect on the responses to PDGF. We conclude that differences between the [Ca2+]i responses to bombesin and PDGF, previously reported using cell populations, reflect differences occurring in individual cells, and that the [Ca2+]i responses to bombesin, vasopressin, and PGF2 alpha (but not PDGF) are subject to feedback inhibition via protein kinase C.

摘要

单细胞荧光图像分析已被用于表征在对照和蛋白激酶C缺失的瑞士3T3细胞中,有丝分裂原诱导的细胞内游离[Ca2+]([Ca2+]i)的增加。超过80%的对照细胞对蛙皮素、血管加压素或前列腺素F2α(PGF2α)表现出快速、短暂的反应。相比之下,血小板衍生生长因子(PDGF)诱导的[Ca2+]i反应明显更具异质性、更慢,且通常为双相性,只有较少的细胞(60-70%)产生反应。对每种有丝分裂原产生反应所获得的[Ca2+]i峰值在细胞之间显示出很大差异。用12-O-十四酰佛波醇13-乙酸酯(TPA)对细胞进行短暂预处理可降低对蛙皮素的[Ca2+]i反应,但不影响对PDGF的反应。用TPA对细胞进行长期预处理以下调蛋白激酶C,导致对蛙皮素、血管加压素和PGF2α的[Ca2+]i反应显著延长,但对PDGF的反应没有这种影响。我们得出结论,之前使用细胞群体报道的对蛙皮素和PDGF的[Ca2+]i反应之间的差异反映了单个细胞中发生的差异,并且对蛙皮素、血管加压素和PGF2α(但不是PDGF)的[Ca2+]i反应受到通过蛋白激酶C的反馈抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a22f/361427/dcc0eec7c3ec/cellregul00038-0090-a.jpg

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