In cell biology, active transport refers to the process by which molecules or ions move across a cell membrane from an area of low concentration to an area of high concentration. This process is against the concentration gradient and requires the support of cellular energy. Active transport is generally divided into two types: primary active transport (mainly utilizing adenosine triphosphate, ATP) and secondary active transport (utilizing electrochemical gradients). This is in contrast to passive transport, which requires no energy and allows molecules or ions to move from areas of high concentration to areas of low concentration.
Active transport is crucial in various physiological processes, such as nutrient uptake, hormone secretion, and nerve impulse transmission.
The concept of active transport began in 1848, when the German physiologist Emile Dubois-Raymond proposed the possibility of actively transporting substances through membranes. In 1926, Denis Robert Hockland studied how plants absorb salt across concentration gradients and discovered that nutrient uptake and transport depended on metabolic energy. In 1948, Rosenberg proposed the concept of active transport based on energy considerations; and in 1997, Danish doctor Jens Christian Skow won the Nobel Prize in Chemistry for his research on the sodium-potassium pump.
Specialized transmembrane proteins recognize and allow substances to pass through the membrane that would otherwise be difficult to pass through, or that require transport against a concentration gradient. There are two main forms in the active transport process: first active transport and second active transport. The first active transport relies on chemical energy (such as ATP), while the second active transport exploits the electrochemical gradient created by pumping ions. For one substance to move against its electrochemical gradient, another substance may move against its concentration gradient.
If matrix molecules move from an area of low concentration to an area of high concentration, this process requires specific transmembrane transport proteins.
In the first active transport, common Nessler electrolytes (such as Na+, K+, etc.) need to cross the cell membrane in the form of ion pumps. Take the sodium-potassium pump, for example, which is a typical ATPase that helps maintain membrane potential within cells. Examples of secondary active transport include sodium-glucose co-transporters (SGLTs), which use the energy of the inward flow of sodium ions to facilitate glucose uptake.
In the human intestine, active absorption of glucose is an example of active transport. Plant root hair cells also use active transport to absorb mineral ions present in thin solutions. Of course, ions like chloride and nitrate require a hydrogen pump to transport them into the cell's vacuoles against the concentration gradient.
Whether it is primary active transport or secondary active transport, active transport is the key for cells to survive in adversity.
Dysregulation of active transport can lead to various diseases. For example, cystic fibrosis is caused by malfunctioning chloride channels, while diabetes results from defects in the transport of glucose into cells. Understanding active transport is crucial for the treatment of these diseases, especially by studying co-transporters and other related transport proteins, so that scientists can develop novel treatment options.
Active transport is not only a key mechanism in cellular physiological processes, but also an important force for cells to resist adversity. By gaining a deeper understanding of this transport process, scientists hope to find more ways to treat disease. How do cells use this mechanism to survive and reproduce in adversity? Can it provide us with more clues to the mysteries of life?