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1
Interstitial Cajal-like cells (ICLC) in atrial myocardium: ultrastructural and immunohistochemical characterization.心房心肌中的间质 Cajal 样细胞(ICLC):超微结构和免疫组织化学特征
J Cell Mol Med. 2006 Jan-Mar;10(1):243-57. doi: 10.1111/j.1582-4934.2006.tb00306.x.
2
Interstitial cells of Cajal in the deep muscular plexus mediate enteric motor neurotransmission in the mouse small intestine.深部肌丛中的 Cajal 间质细胞介导小鼠小肠的肠运动神经传递。
J Physiol. 2006 May 15;573(Pt 1):147-59. doi: 10.1113/jphysiol.2006.105189. Epub 2006 Mar 2.
3
Vascular Na+/Ca2+ exchanger: implications for the pathogenesis and therapy of salt-dependent hypertension.血管钠/钙交换器:对盐依赖性高血压发病机制及治疗的意义
Am J Physiol Regul Integr Comp Physiol. 2006 Mar;290(3):R536-45. doi: 10.1152/ajpregu.00592.2005.
4
Interstitial cells of cajal as pacemakers in the gastrointestinal tract.胃肠道中作为起搏细胞的 Cajal 间质细胞。
Annu Rev Physiol. 2006;68:307-43. doi: 10.1146/annurev.physiol.68.040504.094718.
5
Aortic smooth muscle and endothelial plasma membrane Ca2+ pump isoforms are inhibited differently by the extracellular inhibitor caloxin 1b1.细胞外抑制剂钙调素1b1对主动脉平滑肌和内皮细胞质膜Ca2+泵同工型的抑制作用存在差异。
Am J Physiol Cell Physiol. 2006 May;290(5):C1341-9. doi: 10.1152/ajpcell.00573.2005. Epub 2006 Feb 1.
6
Ca2+ clearance in smooth muscle: lessons from gene-altered mice.平滑肌中的钙离子清除:基因改造小鼠带来的启示。
J Smooth Muscle Res. 2005 Oct;41(5):235-45. doi: 10.1540/jsmr.41.235.
7
Colocalization between caveolin isoforms in the intestinal smooth muscle and interstitial cells of Cajal of the Cav1(+/+) and Cav1 (-/-) mouse.Cav1(+/+)和Cav1 (-/-)小鼠肠道平滑肌和 Cajal间质细胞中小窝蛋白亚型之间的共定位。
Histochem Cell Biol. 2006 Jul;126(1):9-16. doi: 10.1007/s00418-005-0128-3. Epub 2005 Dec 20.
8
Interstitial Cajal-like cells (ICLC) in human resting mammary gland stroma. Transmission electron microscope (TEM) identification.人静止乳腺基质中的间质 Cajal 样细胞(ICLC)。透射电子显微镜(TEM)鉴定。
J Cell Mol Med. 2005 Oct-Dec;9(4):893-910. doi: 10.1111/j.1582-4934.2005.tb00387.x.
9
Plasma membrane calcium pumps in smooth muscle: from fictional molecules to novel inhibitors.平滑肌中的质膜钙泵:从虚构分子到新型抑制剂
Can J Physiol Pharmacol. 2005 Aug-Sep;83(8-9):743-54. doi: 10.1139/y05-075.
10
TRPV4 forms a novel Ca2+ signaling complex with ryanodine receptors and BKCa channels.瞬时受体电位香草酸亚型4(TRPV4)与兰尼碱受体和大电导钙激活钾通道(BKCa通道)形成一种新型的钙离子信号复合体。
Circ Res. 2005 Dec 9;97(12):1270-9. doi: 10.1161/01.RES.0000194321.60300.d6. Epub 2005 Nov 3.

小窝与钙处理:综述与假说

Caveolae and calcium handling, a review and a hypothesis.

作者信息

Daniel E E, El-Yazbi A, Cho W J

机构信息

Department Of Pharmacology, University of Alberta, Edmonton, Canada.

出版信息

J Cell Mol Med. 2006 Apr-Jun;10(2):529-44. doi: 10.1111/j.1582-4934.2006.tb00418.x.

DOI:10.1111/j.1582-4934.2006.tb00418.x
PMID:16796818
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3933140/
Abstract

Caveolae are associated with molecules crucial for calcium handling. This review considers the roles of caveolae in calcium handling for smooth muscle and interstitial cells of Cajal (ICC). Structural studies showed that the plasma membrane calcium pump (PMCA), a sodium-calcium exchanger (NCX1), and a myogenic nNOS appear to be colocalized with caveolin 1, the main constituent of these caveolae. Voltage dependent calcium channels (VDCC) are associated but not co-localized with caveolin 1, as are proteins of the peripheral sarcoplasmic reticulum (SR) such as calreticulin. Only the nNOS is absent from caveolin 1 knockout animals. Functional studies in calcium free media suggest that a source of calcium in tonic smooth muscles exists, partly sequestered from extracellular EGTA. This source supported sustained contractions to carbachol using VDCC and dependent on activity of the SERCA pump. This source is postulated to be caveolae, near peripheral SR. New evidence, presented here, suggests that a similar source exists in phasic smooth muscle of the intestine and its ICC. These results suggest that caveolae and peripheral SR are a functional unit recycling calcium through VDCC and controlling its local concentration. Calcium handling molecules associated with caveolae in smooth muscle and ICC were identified and their possible functions also reviewed.

摘要

小窝与钙处理的关键分子相关。本综述探讨了小窝在平滑肌和 Cajal 间质细胞(ICC)钙处理中的作用。结构研究表明,质膜钙泵(PMCA)、钠钙交换体(NCX1)和肌源性神经元型一氧化氮合酶(nNOS)似乎与这些小窝的主要成分小窝蛋白 1 共定位。电压依赖性钙通道(VDCC)与小窝蛋白 1 相关但不共定位,外周肌浆网(SR)的蛋白质如钙网蛋白也是如此。只有 nNOS 在小窝蛋白 1 基因敲除动物中不存在。在无钙培养基中的功能研究表明,张力性平滑肌中存在钙源,部分钙源从细胞外乙二醇双四乙酸(EGTA)中隔离。该钙源利用 VDCC 支持对卡巴胆碱的持续收缩,并依赖于肌浆网钙泵(SERCA)的活性。推测该钙源是靠近外周肌浆网的小窝。本文提供的新证据表明,在肠道及其 ICC 的相性平滑肌中也存在类似的钙源。这些结果表明,小窝和外周肌浆网是一个功能单元,通过 VDCC 循环利用钙并控制其局部浓度。鉴定了平滑肌和 ICC 中与小窝相关的钙处理分子,并对其可能的功能进行了综述。