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血管活性药物影响系膜细胞黏附。

Vasoactive agents affect mesangial cell adhesion.

作者信息

Kreisberg J I, Venkatachalam M A

出版信息

Am J Physiol. 1986 Oct;251(4 Pt 1):C505-11. doi: 10.1152/ajpcell.1986.251.4.C505.

Abstract

The formation and maintenance of stress fibers in cultured mesangial cells is associated with myosin light chain phosphorylation [Kreisberg et al. Am. J. Physiol. 249 (Renal Fluid Electrolyte Physiol. 18): F227-F235, 1985], a biochemical indicator for activation of actin-myosin interactions. Agents that elevate intracellular levels of adenosine 3',5'-cyclic monophosphate (cAMP) (e.g., isoproterenol) fragment stress fibers and cause myosin light chain dephosphorylation, whereas the addition of contractile agents such as arginine vasopressin (AVP) and prostaglandin E2 (PGE2) reverses these changes. Because stress fiber development in cultured cells is correlated with tight cell to substrate adhesion, we wanted to examine whether vasoactive agents have an effect on mesangial cell adhesion. Both isoproterenol and dibutyryl cAMP (DBcAMP) reduced mesangial cell adherence as measured by a trypsin assay (% detached cells: control 11 +/- 2.4%; isoproterenol plus isobutylmethylxanthine (IBMX) = 48.3 +/- 7.4%; DBcAMP = 29.3 +/- 3.7%; DBcAMP-IBMX = 73 +/- 4.4%). The areas of focal (adhesive) contacts between the cell and substratum as observed by interference-reflexion microscopy were also reduced, being replaced by areas of greater separation (% of the surface in contact with the substratum: control = 7.4 +/- 0.8%; isoproterenol-IBMX = 2.9 +/- 1.1%). Addition of PGE2 or AVP to the incubation medium containing the cAMP-elevating agents prevented the above changes. PGE2 or AVP alone increased mesangial cell adhesion (% detached cells: control 11 +/- 2.4%; PGE2 = 6.8 +/- 0.5%; AVP = 5.1 +/- 1.2%).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

培养的系膜细胞中应力纤维的形成与维持与肌球蛋白轻链磷酸化有关[克雷斯伯格等人。《美国生理学杂志》249(肾脏液体电解质生理学18):F227 - F235,1985],这是肌动蛋白-肌球蛋白相互作用激活的生化指标。提高细胞内3',5'-环磷酸腺苷(cAMP)水平的药物(如异丙肾上腺素)会使应力纤维断裂并导致肌球蛋白轻链去磷酸化,而添加收缩剂如精氨酸加压素(AVP)和前列腺素E2(PGE2)会逆转这些变化。由于培养细胞中应力纤维的发育与细胞与底物的紧密粘附相关,我们想研究血管活性药物是否对系膜细胞粘附有效应。通过胰蛋白酶测定法测量,异丙肾上腺素和二丁酰cAMP(DBcAMP)均降低了系膜细胞的粘附(脱落细胞百分比:对照组11±2.4%;异丙肾上腺素加异丁基甲基黄嘌呤(IBMX)=48.3±7.4%;DBcAMP = 29.3±3.7%;DBcAMP - IBMX = 73±4.4%)。通过干涉反射显微镜观察到的细胞与底物之间的局灶性(粘附)接触面积也减少了,取而代之的是更大分离区域(与底物接触的表面百分比:对照组 = 7.4±0.8%;异丙肾上腺素 - IBMX = 2.9±1.1%)。向含有升高cAMP药物的孵育培养基中添加PGE2或AVP可防止上述变化。单独的PGE2或AVP增加了系膜细胞的粘附(脱落细胞百分比:对照组11±2.4%;PGE2 = 6.8±0.5%;AVP = 5.1±1.2%)。(摘要截断于250字)

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