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通过青蛙肠系膜毛细血管细胞间裂隙的途径。

Pathways through the intercellular clefts of frog mesenteric capillaries.

作者信息

Adamson R H, Michel C C

机构信息

Department of Physiology & Biophysics, St Mary's Hospital Medical School, Imperial College of Science, Technology & Medicine, London.

出版信息

J Physiol. 1993 Jul;466:303-27.

Abstract
  1. The three-dimensional ultrastructure of endothelial intercellular clefts of frog mesenteric capillaries of known hydraulic permeability (Lp) has been investigated in the absence and presence of lanthanum ions as tracers of extracellular solute. 2. Experiments were carried out on the exposed mesenteries of pithed frogs and Lp of a chosen microvessel perfused with a Ringer solution containing serum albumin (10-40 mg ml-1) was determined. In some experiments the mesentery was fixed in situ with 2.5% glutaraldehyde immediately after Lp had been measured. In other experiments, measurement of Lp was followed by brief microperfusion (10-20 s) with a second Ringer solution containing 1% lanthanum nitrate as a tracer before in situ fixation of the tissue. The tissue was prepared for electron microscopy using standard techniques. The perfused capillary was identified in the block and serial transverse sections were cut along its length over regions where Lp had been measured. 3. In six capillaries where the tissues were fixed immediately after measurement of Lp, Lp had a mean value (+/- S.E.M.) of 4 (+/- 0.5) x 10(-7) cm s-1 (cmH2O)-1. Serial (30-40 nm) sections of these vessels revealed that a single short narrow region of the intercellular clefts ran almost continuously from section to section. Additional tight regions were regularly seen, but they usually extended for relatively few sections. In 13.36 microns of reconstructed cleft, there were three interruptions of the tight region of 0.14, 0.14 and 0.17 microns respectively. In the region of these discontinuities, the wide region was uninterrupted from luminal to abluminal surface. 4. Examination of the tight junction on a tilting stage revealed that the outer leaflets of the adjacent cells were not fused, but separated by a gap of mean width (+/- S.E.M.) 2.3 (+/- 0.1) nm. 5. In four capillaries perfused with lanthanum nitrate before fixation, mean Lp (+/- S.E.M.) was 6.5 (+/- 0.02) x 10(-7) cm s-1 (cmH2O)-1. Segments of intercellular clefts, totalling 23.56 microns in length, were reconstructed from serial sections and throughout these, electron-dense deposits of lanthanum were observed to fill the luminal parts of the intercellular clefts up to the tight region. Lanthanum deposits filled the entire cleft to the abluminal surface at eleven sites, which accounted for a length of 2.52 microns out of the 23.56 microns. Only five of these regions were delimited within a continuous series of sections and their mean length (+/- S.E.M.) was 0.16 (+/- 0.063) microns.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 以镧离子作为细胞外溶质的示踪剂,研究了已知水力传导率(Lp)的青蛙肠系膜毛细血管内皮细胞间裂隙的三维超微结构,实验分有无镧离子两种情况进行。2. 在深度麻醉的青蛙暴露的肠系膜上进行实验,测定灌注含血清白蛋白(10 - 40mg/ml)的林格液的选定微血管的Lp。在一些实验中,Lp测定后立即用2.5%戊二醛原位固定肠系膜。在其他实验中,Lp测定后,在组织原位固定前,先用含1%硝酸镧作为示踪剂的第二种林格液进行短暂微灌注(10 - 20秒)。使用标准技术制备组织用于电子显微镜检查。在包埋块中识别出灌注的毛细血管,并沿其长度在测量Lp的区域切取连续的横切片。3. 在测量Lp后立即固定组织的6根毛细血管中,Lp的平均值(±标准误)为4(±0.5)×10⁻⁷cm·s⁻¹(cmH₂O)⁻¹。这些血管的连续(30 - 40nm)切片显示,细胞间裂隙的单个短而窄的区域在各切片间几乎连续延伸。还经常可见其他紧密区域,但通常延伸的切片相对较少。在13.36微米的重建裂隙中,紧密区域分别有0.14、0.14和0.17微米的三处中断。在这些间断区域,宽区域从管腔表面到管腔外表面是不间断的。4. 在倾斜台上检查紧密连接发现,相邻细胞的外小叶未融合,而是被平均宽度(±标准误)为2.3(±0.1)纳米的间隙隔开。5. 在固定前用硝酸镧灌注的4根毛细血管中,平均Lp(±标准误)为6.5(±0.02)×10⁻⁷cm·s⁻¹(cmH₂O)⁻¹。从连续切片重建了总长度为23.56微米的细胞间裂隙片段,在整个这些片段中,观察到电子致密的镧沉积物填充细胞间裂隙的管腔部分直至紧密区域。在11个部位,镧沉积物填充了整个裂隙直至管腔外表面,在23.56微米的总长度中占2.52微米。这些区域中只有5个在连续的一系列切片中界定,其平均长度(±标准误)为0.16(±0.063)微米。(摘要截于400字)
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd1f/1175480/ec4981824e53/jphysiol00416-0307-a.jpg

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