paracellular flow
Recently Published Documents


TOTAL DOCUMENTS

5
(FIVE YEARS 0)

H-INDEX

3
(FIVE YEARS 0)

F1000Research ◽  
2014 ◽  
Vol 3 ◽  
pp. 304 ◽  
Author(s):  
Richard J. Naftalin

It has been proposed that the non-saturable component of intestinal glucose absorption, apparent following prolonged exposure to high intraluminal glucose concentrations, is mediated via the low affinity glucose and fructose transporter, GLUT2, upregulated within the small intestinal apical border.The evidence that the non-saturable transport component is mediated via an apical membrane sugar transporter is that it is inhibited by phloretin, after exposure to phloridzin. Since the other apical membrane sugar transporter, GLUT5, is insensitive to inhibition by either cytochalasin B, or phloretin, GLUT2 was deduced to be the low affinity sugar transport route.As in its uninhibited state, polarized intestinal glucose absorption depends both on coupled entry of glucose and sodium across the brush border membrane and on the enterocyte cytosolic glucose concentration exceeding that in both luminal and submucosal interstitial fluids, upregulation of GLUT2 within the intestinal brush border will usually stimulate downhill glucose reflux to the intestinal lumen from the enterocytes; thereby reducing, rather than enhancing net glucose absorption across the luminal surface.These states are simulated with a computer model generating solutions to the differential equations for glucose, Na and water flows between luminal, cell, interstitial and capillary compartments. The model demonstrates that uphill glucose transport via SGLT1 into enterocytes, when short-circuited by any passive glucose carrier in the apical membrane, such as GLUT2, will reduce transcellular glucose absorption and thereby lead to increased paracellular flow. The model also illustrates that apical GLUT2 may usefully act as an osmoregulator to prevent excessive enterocyte volume change with altered luminal glucose concentrations.


2003 ◽  
Vol 161 (5) ◽  
pp. 979-989 ◽  
Author(s):  
Jennifer L. Genova ◽  
Richard G. Fehon

One essential function of epithelia is to form a barrier between the apical and basolateral surfaces of the epithelium. In vertebrate epithelia, the tight junction is the primary barrier to paracellular flow across epithelia, whereas in invertebrate epithelia, the septate junction (SJ) provides this function. In this study, we identify new proteins that are required for a functional paracellular barrier in Drosophila. In addition to the previously known components Coracle (COR) and Neurexin (NRX), we show that four other proteins, Gliotactin, Neuroglian (NRG), and both the α and β subunits of the Na+/K+ ATPase, are required for formation of the paracellular barrier. In contrast to previous reports, we demonstrate that the Na pump is not localized basolaterally in epithelial cells, but instead is concentrated at the SJ. Data from immunoprecipitation and somatic mosaic studies suggest that COR, NRX, NRG, and the Na+/K+ ATPase form an interdependent complex. Furthermore, the observation that NRG, a Drosophila homologue of vertebrate neurofascin, is an SJ component is consistent with the notion that the invertebrate SJ is homologous to the vertebrate paranodal SJ. These findings have implications not only for invertebrate epithelia and barrier functions, but also for understanding of neuron–glial interactions in the mammalian nervous system.


1986 ◽  
Vol 123 (1) ◽  
pp. 71-92
Author(s):  
GUILLERMO WHITTEMBURY ◽  
ANGELA C. BIONDI ◽  
AZAEL PAZ-ALIAGA ◽  
HENRY LINARES ◽  
VALENTÍN PARTHE ◽  
...  

The following molecules graded in size were added to the fluid bathing the blind end of the upper segment of the Malpighian tubules of Rhodnius: urea (U), erythritol (E), mannitol (M), L-glucose (G), sucrose (S), polyethyleneglycol 800 (PEG), raffinose (R), inulin (I) and dextran 15000–18000 (D). U, E, M and G distribute themselves within the cell and the extracellular space, while S, PEG, R, I and D are exclusively extracellular. In addition, the net secretory flow (Jnm8) of these probes was studied as a function of the net secretory volume flow (Jv). Jn8, is made up of a diffusive component (Jd8), mainly due to unstirred layer effects, and of a convective component (Jc8), due to the drag (entrainment) of the probes by the water flow. The relative contribution of Jd8 and of Jc8 for each probe was studied as a function of Jv. It was found that Jc8 >> Jd8 for U, E, M, G, S and PEG. Therefore these probes are dragged by water. On the other hand Jd8 = Jn8 for R, I and D, which are not entrained. It is concluded that water flows via extracellular pathways since S and PEG, which are true extracellular probes, are entrained by solvent. In addition to extracellular pathways, it is suggested that the transcellular structures described by Wessing (1965) and Bergeron et al. (1985) could also be the sites of solute-solvent coupling


1977 ◽  
Vol 233 (5) ◽  
pp. R198-R207
Author(s):  
G. A. Ahearn ◽  
N. F. Hadley

Water transport in desert scorpion ileum involves two independent transfer pathways operating in parallel: 1) paracellular flow occurs through intercellular spaces in response to transmural osmotic or ionic gradients; and 2) transcellular water transport occurs across apical and basal cell membranes in response to a basal, energy-requiring sodium efflux process. The tissue exhibits no osmotic rectification over the range of transepithelial osmotic gradients imposed (Lp = hydraulic conductivity), Lp = 95 x 10(-7) cm - s-1 - atm-1), but displays apparent asymmetric ion permeability in response to transmural ion gradients, as determined by codiffusional water movements across the preparation. Osmotic permeability ((Pos), Pos = 1.13 x 10(-3) cm - s-1) of the tissue exceeds diffusional permeability ((Pd), Pd = 1.45 x 10(-5) cm - s-1) by almost two orders of magnitude. In the absence of osmotic or hydrostatic pressure gradients, transmural water transport requires cellular metabolism, is sodium-dependent, is inhibited by potassium, and produces an apparent strongly hypotonic absorbate. This water transport process appears to be adaptive, as scorpion dehydration results in alterations of luminal ion concentrations that favor increased net flow of water to the hemolymph.


1976 ◽  
Vol 71 (3) ◽  
pp. 967-972 ◽  
Author(s):  
B A Lord ◽  
D R DiBona

A comparison of the distribution of septate junctions in invertebrate epithelia and tight junctions in vertebrate systems suggests that these structures may be functionally analogous. This proposition is supported by the internal design of each junction which constitutes a serial arrangement of structures crossing the intercellular space between cells to effectively provide resistance to the paracellular flow of water and small molecules. We have tested the validity of such an analogy by examining whether the osmotic sensitivity of the septate junctions of planarian epidermis follow the rather striking pattern observed for the junctions of very tight vertebrate epithelia (e.g. toad urinary bladder). It has been found that the septate junctions in this system respond in similar fashion to their vertebrate counterparts, blistering with accumulated fluid when the medium outside the epidermis is made hypertonic with small, water-soluble molecules. We conclude that the two types of junction probably are functionally analogous and that, in each case, this rectified structural response to transepithelial osmotic gradients may be indicative of the role of such structures in the transport function of epithelia.


Sign in / Sign up

Export Citation Format

Share Document