Molecular transport at cell membranes

It has become increasingly evident during the last decade that cell membranes are equipped with factors that play specific roles in conveying both inorganic and organic substances from the cell exterior to the cell interior or from one compartment in the cell to another. The normal diffusion processes (often called passive diffusion) occur but these may be slow, the rates depending on the concentrations of the substances involved. Passive diffusion leads only to a concentration within the cell no higher than that outside except under circumstances where binding of the substance, to a cell constituent, takes place in the cell or in a cell compartment. The components in the cell membrane that control the rates of ionic and molecular transport, and which may lead to the attainment of concentrations of ions and molecules in the cell substantially higher than those outside, may play roles as important as those of the enzymes in the control of cell growth, metabolism and function. The process whereby a substance is transferred across the cell membrane in such a manner that it is specifically controlled, that it can lead to accumulation of the substance in the cell against a concentration gradient, and that it is energy assisted, i. e. coupled with metabolic processes, is often referred to as active transport. The specific components located at the cell membrane and involved in the transport processes are usually termed transport carriers.

2022 ◽  
Vol 1 (6) ◽  
pp. 149-162
Author(s):  
Rara Inggarsih ◽  
Ella Amalia ◽  
Septi Purnamasari

The cell membrane plays an important role in cell traffic because it functions to secrete various molecules. The selective transport system allows the movement of molecules into or out of the cell compartment. By controlling the movement of substances from one compartment to another, membranes exert a strong influence on metabolic pathways. Cell membranes are composed of proteins and lipids with a very important function in maintaining the rhythm of circulation and cell transport. In addition, the cell membrane also plays a role in maintaining the integrity and relationship, and communication of cells.


1978 ◽  
Vol 26 (4) ◽  
pp. 293-297 ◽  
Author(s):  
W Bohn

A fixation method for electron microscopical immunoperoxidase staining has been developed, which (a) allows penetration of antibodies through cell membranes to intracellular antigen sites, (b) provides a reasonable cell preservation and (c) does not alter the antigenic structure in too great an extent. Penetration of the antibodies has been achieved by using saponin as a cell membrane attacking agent. The best results could be obtained after pretreatment of cell monolayers with a mixture of 0.05% saponin, 0.0125%-0.05% glutaraldehyde and 1% paraformaldehyde for 5 min at 4 degrees C, and postfixing them with the corresponding fixative without saponin for 45 min at 4 degrees C.


1986 ◽  
Vol 71 (3) ◽  
pp. 225-230 ◽  
Author(s):  
Robert F. Bing ◽  
Anthony M. Heagerty ◽  
Herbert Thurston ◽  
John D. Swales

Disturbances in several, distinct cell membrane ion transport processes have been demonstrated in essential hypertension but their variable relationship to blood pressure in different populations has made it difficult to achieve a unifying hypothesis. We suggest that altered composition of the lipid fraction of the cell membrane is the common underlying factor. This would produce many of the reported perturbations of cell membrane properties and function, not all of which relate directly to the development of hypertension, but which act as markers for the underlying abnormality. However, functions such as phosphoinositol turnover, calcium binding and Ca2+,Mg2+-ATPase dependent calcium efflux, which are influenced by the lipid composition of the membrane, provide a possible link between the membrane disturbance, intracellular calcium, vascular smooth muscle contraction and blood pressure. Alteration in the lipid content of the cell membrane not only provides an explanation for the variability in the ion transport abnormalities between populations but perhaps also for some of the variability in blood pressure within a single population. It also provides a potential means of influencing blood pressure by dietary intervention.


Physiology ◽  
1997 ◽  
Vol 12 (1) ◽  
pp. 49-53 ◽  
Author(s):  
Arnost Kleinzeller

In a series of three lectures in 1895-1899, Charles Ernest Overton (1865-1933) pioneered three fundamental concepts of the structure and function of cell membranes: 1) the lipid theory of cell permeability, 2) the lipid theory of narcosis, and 3) the involvement of an Na+/K+ exchange in muscle and nerve excitability.


2019 ◽  
Vol 6 (3) ◽  
pp. 551-561 ◽  
Author(s):  
Mingjun Xuan ◽  
Jingxin Shao ◽  
Junbai Li

Abstract Surface engineering of synthetic carriers is an essential and important strategy for drug delivery in vivo. However, exogenous properties make synthetic nanosystems invaders that easily trigger the passive immune clearance mechanism, increasing the retention effect caused by the reticuloendothelial systems and bioadhesion, finally leading to low therapeutic efficacy and toxic effects. Recently, a cell membrane cloaking technique has been reported as a novel interfacing approach from the biological/immunological perspective, and has proved useful for improving the performance of synthetic nanocarriers in vivo. After cell membrane cloaking, nanoparticles not only acquire the physiochemical properties of natural cell membranes but also inherit unique biological functions due to the presence of membrane-anchored proteins, antigens, and immunological moieties. The derived biological properties and functions, such as immunosuppressive capability, long circulation time, and targeted recognition integrated in synthetic nanosystems, have enhanced their potential in biomedicine in the future. Here, we review the cell membrane-covered nanosystems, highlight their novelty, introduce relevant biomedical applications, and describe the future prospects for the use of this novel biomimetic system constructed from a combination of cell membranes and synthetic nanomaterials.


Author(s):  
Wei Yuan ◽  
Jiafang Piao ◽  
Yuanchen Dong

In order to better understand the structure and function of the biological cell membrane, various artificial systems have been developed. Among them, unilamellar lipid vesicles (liposomes)-based artificial cell membranes have...


2011 ◽  
Vol 76 (6) ◽  
pp. 683-694 ◽  
Author(s):  
Alexis E. Abelow ◽  
Ryan J. White ◽  
Kevin W. Plaxco ◽  
Ilya Zharov

We report the preparation of colloidal nanoporous silica films whose function mimics that of protein channels in gating the transport of small molecules across a cell membrane. Specifically, we report a means of controlling the molecular flux through colloidal nanopores that employ aptamer oligonucleotides binding to a specific organic small molecule (cocaine). These biomacromolecules have been introduced onto the nanopore surface by attaching pre-made oligonucleotides to the activated nanopore surface. The aptamers change their conformation in response to the binding events, and thus alter the free volume of the colloidal nanopores available for molecular transport.


2020 ◽  
Vol 16 (34) ◽  
pp. 2853-2861
Author(s):  
Yanli Li ◽  
Rui Yang ◽  
Limo Chen ◽  
Sufang Wu

CD38 is a transmembrane glycoprotein that is widely expressed in a variety of human tissues and cells, especially those in the immune system. CD38 protein was previously considered as a cell activation marker, and today monoclonal antibodies targeting CD38 have witnessed great achievements in multiple myeloma and promoted researchers to conduct research on other tumors. In this review, we provide a wide-ranging review of the biology and function of the human molecule outside the field of myeloma. We focus mainly on current research findings to summarize and update the findings gathered from diverse areas of study. Based on these findings, we attempt to extend the role of CD38 in the context of therapy of solid tumors and expand the role of the molecule from a simple marker to an immunomodulator.


Author(s):  
Vitalii Kryvenko ◽  
Olga Vagin ◽  
Laura A. Dada ◽  
Jacob I. Sznajder ◽  
István Vadász

Abstract The Na,K-ATPase establishes the electrochemical gradient of cells by driving an active exchange of Na+ and K+ ions while consuming ATP. The minimal functional transporter consists of a catalytic α-subunit and a β-subunit with chaperon activity. The Na,K-ATPase also functions as a cell adhesion molecule and participates in various intracellular signaling pathways. The maturation and trafficking of the Na,K-ATPase include co- and post-translational processing of the enzyme in the endoplasmic reticulum (ER) and the Golgi apparatus and subsequent delivery to the plasma membrane (PM). The ER folding of the enzyme is considered as the rate-limiting step in the membrane delivery of the protein. It has been demonstrated that only assembled Na,K-ATPase α:β-complexes may exit the organelle, whereas unassembled, misfolded or unfolded subunits are retained in the ER and are subsequently degraded. Loss of function of the Na,K-ATPase has been associated with lung, heart, kidney and neurological disorders. Recently, it has been shown that ER dysfunction, in particular, alterations in the homeostasis of the organelle, as well as impaired ER-resident chaperone activity may impede folding of Na,K-ATPase subunits, thus decreasing the abundance and function of the enzyme at the PM. Here, we summarize our current understanding on maturation and subsequent processing of the Na,K-ATPase in the ER under physiological and pathophysiological conditions. Graphic Abstract


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