Passive transport

Short description: Transport that does not require energy

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Passive diffusion across a cell membrane.

Passive transport is a type of membrane transport that does not require energy to move substances across cell membranes.[1][2] Instead of using cellular energy, like active transport,[3] passive transport relies on the second law of thermodynamics to drive the movement of substances across cell membranes.[1][2][4] Fundamentally, substances follow Fick's first law, and move from an area of high concentration to one of low concentration because this movement increases the entropy of the overall system.[4][5] The rate of passive transport depends on the permeability of the cell membrane, which, in turn, depends on the organization and characteristics of the membrane lipids and proteins.[citation needed] The four main kinds of passive transport are simple diffusion, facilitated diffusion, filtration, and/or osmosis.

Passive transport follows Fick's first law.

## Contents

* 1 Diffusion
* 1.1 Example of diffusion: Gas Exchange
* 2 Facilitated diffusion
* 2.1 Example of facilitated diffusion: GLUT2
* 3 Filtration
* 4 Osmosis
* 5 See also
* 6 References

## Diffusion

Passive diffusion on a cell membrane.

Diffusion is the net movement of material from an area of high concentration to an area with lower concentration. The difference of concentration between the two areas is often termed as the concentration gradient, and diffusion will continue until this gradient has been eliminated. Since diffusion moves materials from an area of higher concentration to an area of lower concentration, it is described as moving solutes "down the concentration gradient" (compared with active transport, which often moves material from area of low concentration to area of higher concentration, and therefore referred to as moving the material "against the concentration gradient"). However, in many cases (e.g. passive drug transport) the driving force of passive transport can not be simplified to the concentration gradient. If there are different solutions at the two sides of the membrane with different equilibrium solubility of the drug, the difference in the degree of saturation is the driving force of passive membrane transport.[6] It is also true for supersaturated solutions which are more and more important owing to the spreading of the application of amorphous solid dispersions for drug bioavailability enhancement.

Simple diffusion and osmosis are in some ways similar. Simple diffusion is the passive movement of solute from a high concentration to a lower concentration until the concentration of the solute is uniform throughout and reaches equilibrium. Osmosis is much like simple diffusion but it specifically describes the movement of water (not the solute) across a selectively permeable membrane until there is an equal concentration of water and solute on both sides of the membrane. Simple diffusion and osmosis are both forms of passive transport and require none of the cell's ATP energy.

### Example of diffusion: Gas Exchange

A biological example of diffusion is the gas exchange that occurs during respiration within the human body.[7] Upon inhalation, oxygen is brought into the lungs and quickly diffuses across the membrane of alveoli and enters the circulatory system by diffusing across the membrane of the pulmonary capillaries.[8] Simultaneously, carbon dioxide moves in the opposite direction, diffusing across the membrane of the capillaries and entering into the alveoli, where it can be exhaled. The process of moving oxygen into the cells, and carbon dioxide out, occurs because of the concentration gradient of these substances, each moving away from their respective areas of higher concentration toward areas of lower concentration.[7][8] Cellular respiration is the cause of the low concentration of oxygen and high concentration of carbon dioxide within the blood which creates the concentration gradient. Because the gasses are small and uncharged, they are able to pass directly through the cell membrane without any special membrane proteins.[9] No energy is required because the movement of the gasses follows Fick's first law and the second law of thermodynamics.

## Facilitated diffusion

Depiction of facilitated diffusion.

Facilitated diffusion, also called carrier-mediated osmosis, is the movement of molecules across the cell membrane via special transport proteins that are embedded in the plasma membrane by actively taking up or excluding ions. Active transport of protons by H+ ATPases[10] alters membrane potential allowing for facilitated passive transport of particular ions such as potassium [11] down their charge gradient through high affinity transporters and channels.

### Example of facilitated diffusion: GLUT2

An example of facilitated diffusion is when glucose is absorbed into cells through Glucose transporter 2 (GLUT2) in the human body.[12][13] There are many other types of glucose transport proteins, some that do require energy, and are therefore not examples of passive transport.[13] Since glucose is a large molecule, it requires a specific channel to facilitate its entry across plasma membranes and into cells.[13] When diffusing into a cell through GLUT2, the driving force that moves glucose into the cell is still the concentration gradient.[12] The main difference between simple diffusion and facilitated diffusion is that facilitated diffusion requires a transport protein to 'facilitate' or assist the substance through the membrane.[14] After a meal, the cell is signaled to move GLUT2 into membranes of the cells lining the intestines called enterocytes.[12] With GLUT2 in place after a meal and the relative high concentration of glucose outside of these cells as compared to within them, the concentration gradient drives glucose across the cell membrane through GLUT2.[12][13]

## Filtration

Filtration.

Filtration is movement of water and solute molecules across the cell membrane due to hydrostatic pressure generated by the cardiovascular system. Depending on the size of the membrane pores, only solutes of a certain size may pass through it. For example, the membrane pores of the Bowman's capsule in the kidneys are very small, and only albumins, the smallest of the proteins, have any chance of being filtered through. On the other hand, the membrane pores of liver cells are extremely large, but not forgetting cells are extremely small to allow a variety of solutes to pass through and be metabolized.

## Osmosis

Main pages: Physics:Osmosis  and Biology:Tonicity

Effect of osmosis on blood cells under different solutions.

Osmosis is the movement of water molecules across a selectively permeable membrane. The net movement of water molecules through a partially permeable membrane from a solution of high water potential to an area of low water potential. A cell with a less negative water potential will draw in water but this depends on other factors as well such as solute potential (pressure in the cell e.g. solute molecules) and pressure potential (external pressure e.g. cell wall). There are three types of Osmosis solutions: the isotonic solution, hypotonic solution, and hypertonic solution. Isotonic solution is when the extracellular solute concentration is balanced with the concentration inside the cell. In the Isotonic solution, the water molecules still move between the solutions, but the rates are the same from both directions, thus the water movement is balanced between the inside of the cell as well as the outside of the cell. A hypotonic solution is when the solute concentration outside the cell is lower than the concentration inside the cell. In hypotonic solutions, the water moves into the cell, down its concentration gradient (from higher to lower water concentrations). That can cause the cell to swell. Cells that don't have a cell wall, such as animal cells, could burst in this solution. A hypertonic solution is when the solute concentration is higher (think of hyper - as high) than the concentration inside the cell. In hypertonic solution, the water will move out, causing the cell to shrink.

## See also

* Active transport
* Transport phenomena

## References

1. ↑ 1.0 1.1 "5.2 Passive Transport - Biology 2e | OpenStax" (in en). https://openstax.org/books/biology-2e/pages/5-2-passive-transport.
2. ↑ 2.0 2.1 "5.2A: The Role of Passive Transport" (in en). 2018-07-10. https://bio.libretexts.org/Bookshelves/Introductory_and_General_Biology/Book:_General_Biology_(Boundless)/5:_Structure_and_Function_of_Plasma_Membranes/5.2:_Passive_Transport/5.2A:_The_Role_of_Passive_Transport.
3. ↑ "5.3 Active Transport - Biology 2e | OpenStax" (in en). https://openstax.org/books/biology-2e/pages/5-3-active-transport.
4. ↑ 4.0 4.1 Skene, Keith R. (2015). "Life's a Gas: A Thermodynamic Theory of Biological Evolution" (in en). Entropy 17 (8): 5522–5548. doi:10.3390/e17085522. Bibcode: 2015Entrp..17.5522S.
5. ↑ "12.7 Molecular Transport Phenomena: Diffusion, Osmosis, and Related Processes - College Physics for AP® Courses | OpenStax" (in en). https://openstax.org/books/college-physics-ap-courses/pages/12-7-molecular-transport-phenomena-diffusion-osmosis-and-related-processes.
6. ↑ Borbas, E. (2016). "Investigation and Mathematical Description of the Real Driving Force of Passive Transport of Drug Molecules from Supersaturated Solutions". Molecular Pharmaceutics 13 (11): 3816–3826. doi:10.1021/acs.molpharmaceut.6b00613. PMID 27611057.
7. ↑ 7.0 7.1 Wagner, Peter D. (2015-01-01). "The physiological basis of pulmonary gas exchange: implications for clinical interpretation of arterial blood gases" (in en). European Respiratory Journal 45 (1): 227–243. doi:10.1183/09031936.00039214. ISSN 0903-1936. PMID 25323225. https://erj.ersjournals.com/content/45/1/227.
8. ↑ 8.0 8.1 "22.4 Gas Exchange - Anatomy and Physiology | OpenStax" (in en). https://openstax.org/books/anatomy-and-physiology/pages/22-4-gas-exchange.
9. ↑ "3.1 The Cell Membrane - Anatomy and Physiology | OpenStax" (in en). https://openstax.org/books/anatomy-and-physiology/pages/3-1-the-cell-membrane.
10. ↑ Palmgren, Michael G. (2001-01-01). "PLANT PLASMA MEMBRANE H+-ATPases: Powerhouses for Nutrient Uptake". Annual Review of Plant Physiology and Plant Molecular Biology 52 (1): 817–845. doi:10.1146/annurev.arplant.52.1.817. PMID 11337417.
11. ↑ Dreyer, Ingo; Uozumi, Nobuyuki (2011-11-01). "Potassium channels in plant cells" (in en). FEBS Journal 278 (22): 4293–4303. doi:10.1111/j.1742-4658.2011.08371.x. ISSN 1742-4658. PMID 21955642.
12. ↑ 12.0 12.1 12.2 12.3 Kellett, George L.; Brot-Laroche, Edith; Mace, Oliver J.; Leturque, Armelle (2008). "Sugar absorption in the intestine: the role of GLUT2". Annual Review of Nutrition 28: 35–54. doi:10.1146/annurev.nutr.28.061807.155518. ISSN 0199-9885. PMID 18393659. https://pubmed.ncbi.nlm.nih.gov/18393659/.
13. ↑ 13.0 13.1 13.2 13.3 Chen, Lihong; Tuo, Biguang; Dong, Hui (2016-01-14). "Regulation of Intestinal Glucose Absorption by Ion Channels and Transporters". Nutrients 8 (1): 43. doi:10.3390/nu8010043. ISSN 2072-6643. PMID 26784222.
14. ↑ Cooper, Geoffrey M. (2000). "Transport of Small Molecules" (in en). The Cell: A Molecular Approach. 2nd Edition. https://www.ncbi.nlm.nih.gov/books/NBK9847/.

* Alcamo, I. Edward (1997). "Chapter 2–5: Passive transport". Biology coloring workbook. Illustrations by John Bergdahl. New York: Random House. pp. 24–25. ISBN 9780679778844.
* Sadava, David; H. Craig Heller; Gordon H. Orians; William K. Purves; David M. Hillis (2007). "What are the passive processes of membrane transport?". Life : the science of biology (8th ed.). Sunderland, MA: Sinauer Associates. pp. 105–110. ISBN 9780716776710. https://archive.org/details/lifescienceofbio00davi/page/105.
* Srivastava, P. K. (2005). Elementary biophysics : an introduction. Harrow: Alpha Science Internat.. pp. 140–148. ISBN 9781842651933.

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Membrane transport

Mechanisms for chemical transport through biological membranes

Passive transport|

* Simple diffusion (or non-mediated transport)
* Facilitated diffusion
* Osmosis
* Channels
* Carriers

Active transport|

* Uniporter
* Symporter
* Antiporter
* Primary active transport
* Secondary active transport

Cytosis|

| Endocytosis|

* Efferocytosis
* Non-specific, adsorptive pinocytosis
* Phagocytosis
* Pinocytosis
* Potocytosis
* Receptor-mediated endocytosis
* Transcytosis

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Exocytosis|

Degranulation

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