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本文引用的文献

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Patch-clamp recordings of the light-sensitive dark noise in retinal rods from the lizard and frog.对蜥蜴和青蛙视网膜视杆细胞中光敏暗噪声的膜片钳记录。
J Physiol. 1985 Oct;367:183-216. doi: 10.1113/jphysiol.1985.sp015820.
2
Calcium and light adaptation in retinal rods and cones.视网膜视杆细胞和视锥细胞中的钙与光适应
Nature. 1988 Jul 7;334(6177):69-71. doi: 10.1038/334069a0.
3
Ion transport by the Na-Ca exchange in isolated rod outer segments.分离的视杆细胞外段中钠钙交换介导的离子转运。
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4548-52. doi: 10.1073/pnas.85.12.4548.
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Hindered diffusion in excised membrane patches from retinal rod outer segments.视网膜视杆细胞外段切除膜片中的受限扩散。
Biophys J. 1988 Aug;54(2):351-5. doi: 10.1016/S0006-3495(88)82966-7.
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Role of calcium in regulating the cyclic GMP cascade of phototransduction in retinal rods.钙在调节视网膜视杆细胞光转导的环鸟苷酸级联反应中的作用。
Proc Natl Acad Sci U S A. 1986 Sep;83(18):7109-13. doi: 10.1073/pnas.83.18.7109.
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Guanosine 3',5'-cyclic monophosphate stimulates release of actively accumulated calcium in purified disks from rod outer segments of bovine retina.3',5'-环磷酸鸟苷刺激牛视网膜视杆外段纯化盘膜中主动积累的钙的释放。
Biochemistry. 1986 Apr 8;25(7):1739-46. doi: 10.1021/bi00355a044.
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Stabilization of phosphofructokinase with sugars during freeze-drying: characterization of enhanced protection in the presence of divalent cations.冷冻干燥过程中糖对磷酸果糖激酶的稳定作用:二价阳离子存在下增强保护作用的表征
Biochim Biophys Acta. 1987 Jan 20;923(1):109-15. doi: 10.1016/0304-4165(87)90133-4.
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Evidence for two functionally different membrane fractions in bovine retinal rod outer segments.牛视网膜视杆细胞外段中两种功能不同的膜组分的证据。
J Physiol. 1988 Jul;401:309-27. doi: 10.1113/jphysiol.1988.sp017164.
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Solubilization, purification, and reconstitution of the sodium-calcium exchanger from bovine retinal rod outer segments.牛视网膜视杆细胞外段钠钙交换体的增溶、纯化及重组。
J Biol Chem. 1988 Aug 15;263(23):11382-8.
10
Sodium ions selectively eliminate the fast component of guanosine cyclic 3',5'-phosphate induced Ca2+ release from bovine rod outer segment disks.钠离子选择性地消除了鸟苷环3',5'-磷酸诱导的钙离子从牛视杆细胞外节盘膜释放的快速成分。
Biochemistry. 1987 Jun 16;26(12):3249-53. doi: 10.1021/bi00386a002.

牛视网膜视杆细胞外段质膜中环鸟苷酸门控通道与钠钙钾交换体的关联

Association of cyclic GMP-gated channels and Na(+)-Ca(2+)-K+ exchangers in bovine retinal rod outer segment plasma membranes.

作者信息

Bauer P J, Drechsler M

机构信息

Institut für Biologische Informationsverarbeitung, Forschungszentrum Jülich, FRG.

出版信息

J Physiol. 1992;451:109-31. doi: 10.1113/jphysiol.1992.sp019156.

DOI:10.1113/jphysiol.1992.sp019156
PMID:1328615
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1176153/
Abstract
  1. Cyclic GMP-gated channels and Na(+)-Ca(2+)-K+ exchangers from bovine photoreceptors were examined by investigation of the Ca2+ fluxes from vesicles of rod outer segment (ROS) membranes and from proteoliposomes obtained by solubilization of the ROS membrane proteins and reconstitution in soy bean L-alpha-phosphatidylcholine (PC). 2. Whereas vesicles obtained by mild sonication of ROS membranes in a Ca(2+)-containing buffer yielded a maximal cyclic GMP-induced Ca2+ release of about 2.5% and a maximal Na(+)-induced Ca2+ release of about 7%, freezing and thawing of ROS membranes prior to sonication elevated these maximal Ca2+ releases to about 17% for cyclic GMP, and to about 34% for Na+. These observations are in agreement with the view that cyclic GMP-gated channels and Na(+)-Ca(2+)-K+ exchangers are localized only in the plasma membrane of the photoreceptors (which in bovine ROS makes up about 6% of the total membrane), whereas freezing and thawing results in fusion of disc and plasma membranes, thus leading to a distribution of these proteins over a much larger membrane area. 3. For fused ROS membranes, the cyclic GMP-releasable fraction of Ca2+ of 17% is an upper bound; assuming that the cyclic GMP-gated channels are randomly distributed we estimate that about 37% of the vesicles contain at least one cyclic GMP-gated channel. The mean diameter of the vesicles prepared by sonication was determined to be 0.12 +/- 0.04 micron, and therefore the fused ROS membranes contain about sixteen cyclic GMP-gated channels/microns 2. If all cyclic GMP-gated channels originated from the plasma membrane, we estimate that the plasma membrane contains about 270 cyclic GMP-gated channels/microns 2. 4. In vesicles prepared from fused ROS membranes, Na(+)-Ca2+ exchange after activation of the cyclic GMP-gated channels. On the other hand, after an exhaustive Na(+)-Ca2+ exchange, only little, if any, Ca2+ was released upon addition of cyclic GMP, demonstrating that cyclic GMP-gated channels and Na(+)-Ca(2+)-K+ exchangers occur on the same vesicle fraction. This observation suggests that Na(+)-Ca(2+)-K+ exchangers do not distribute independently of the cyclic GMP-gated channels upon membrane fusion but are apparently associated with the cyclic GMP-gated channels.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 通过研究来自视杆外段(ROS)膜囊泡以及通过溶解ROS膜蛋白并在大豆L-α-磷脂酰胆碱(PC)中重构得到的蛋白脂质体中的Ca2+通量,对来自牛感光细胞的环鸟苷酸门控通道和Na(+)-Ca(2+)-K+交换体进行了检测。2. 当在含Ca(2+)的缓冲液中对ROS膜进行温和超声处理得到的囊泡,其环鸟苷酸诱导的最大Ca2+释放量约为2.5%,Na(+)诱导的最大Ca2+释放量约为7%,而在超声处理之前对ROS膜进行冻融处理,则将这些最大Ca2+释放量提高到环鸟苷酸约为17%,Na+约为34%。这些观察结果与以下观点一致,即环鸟苷酸门控通道和Na(+)-Ca(2+)-K+交换体仅位于感光细胞的质膜中(在牛ROS中,质膜约占总膜的6%),而冻融导致盘膜和质膜融合,从而使这些蛋白质分布在大得多的膜面积上。3. 对于融合的ROS膜,环鸟苷酸可释放的Ca2+部分为17%是一个上限;假设环鸟苷酸门控通道随机分布,我们估计约37%的囊泡至少含有一个环鸟苷酸门控通道。通过超声处理制备的囊泡的平均直径确定为0.12±0.04微米,因此融合的ROS膜每平方微米含有约16个环鸟苷酸门控通道。如果所有环鸟苷酸门控通道都来自质膜,我们估计质膜每平方微米含有约270个环鸟苷酸门控通道。4. 在由融合的ROS膜制备的囊泡中,环鸟苷酸门控通道激活后发生Na(+)-Ca2+交换。另一方面,在进行彻底的Na(+)-Ca2+交换后,加入环鸟苷酸时仅释放很少的Ca2+(如果有的话),这表明环鸟苷酸门控通道和Na(+)-Ca(2+)-K+交换体存在于同一囊泡组分上。这一观察结果表明,Na(+)-Ca(2+)-K+交换体在膜融合时并非独立于环鸟苷酸门控通道分布,而是显然与环鸟苷酸门控通道相关联。(摘要截断于400字)