Which hormones have receptors in cell membrane 2nd messenger system activation?

Which hormones have receptors in cell membrane 2nd messenger system activation?

Understanding:

•  Steroid hormones bind to receptor proteins in cytoplasm of target cells to form a receptor-hormone complex

•  The receptor-hormone complex promotes the transcription of specific genes

    
Steroid Hormones

  • Steroid hormones are lipophilic (fat-loving) – meaning they can freely diffuse across the plasma membrane of a cell
  • They bind to receptors in either the cytoplasm or nucleus of the target cell, to form an active receptor-hormone complex
  • This activated complex will move into the nucleus and bind directly to DNA, acting as a transcription factor for gene expression
  • Examples of steroid hormones include those produced by the gonads (i.e. estrogen, progesterone and testosterone)


Which hormones have receptors in cell membrane 2nd messenger system activation?


Which hormones have receptors in cell membrane 2nd messenger system activation?

Understanding:

•  Peptide hormones bind to receptors in the plasma membrane of the target cell

•  Binding to membrane receptors activates a cascade mediated by a second messenger inside the cell

    
Peptide Hormones

  • Peptide hormones are hydrophylic and lipophobic (fat-hating) – meaning they cannot freely cross the plasma membrane
  • They bind to receptors on the surface of the cell, which are typically coupled to internally anchored proteins (e.g. G proteins)
  • The receptor complex activates a series of intracellular molecules called second messengers, which initiate cell activity
  • This process is called signal transduction, because the external signal (hormone) is transduced via internal intermediaries
  • Examples of second messengers include cyclic AMP (cAMP), calcium ions (Ca2+), nitric oxide (NO) and protein kinases
  • The use of second messengers enables the amplification of the initial signal (as more molecules are activated)

    With the exception of the steroid hormones, most hormones such as insulin and glucagon interact with a receptor on the cell surface. The activated receptor then generates so-called second messengers within the cell that transmit the information to the biochemical systems whose activities must be altered to produce a particular physiological effect. The magnitude of the end effect is generally proportional to the concentration of the second messengers.

    An important intracellular second-messenger signaling system, the phosphatidylinositol system, employs two second-messenger lipids, both of which are derived from phosphatidylinositol. One is diacylglycerol (diglyceride), the other is triphosphoinositol. In this system a membrane receptor acts upon an enzyme, phospholipase C, located on the inner surface of the cell membrane. Activation of this enzyme by one of the agents listed in the table causes the hydrolysis of a minor membrane phospholipid, phosphatidylinositol bisphosphate. Without leaving the membrane bilayer, the diacylglycerol next activates a membrane-bound enzyme, protein kinase C, that in turn catalyzes the addition of phosphate groups to a soluble protein. This soluble protein is the first member of a reaction sequence leading to the appropriate physiological response in the cell. The other hydrolysis product of phospholipase C, triphosphoinositol, causes the release of calcium from intracellular stores. Calcium is required, in addition to triacylglycerol, for the activation of protein kinase C.

    Hormones mediate changes in target cells by binding to specific hormone receptors. In this way, even though hormones circulate throughout the body and come into contact with many different cell types, they only affect cells that possess the necessary receptors. Receptors for a specific hormone may be found on many different cells or may be limited to a small number of specialized cells. For example, thyroid hormones act on many different tissue types, stimulating metabolic activity throughout the body. Cells can have many receptors for the same hormone but often also possess receptors for different types of hormones. The number of receptors that respond to a hormone determines the cell’s sensitivity to that hormone, and the resulting cellular response. Additionally, the number of receptors that respond to a hormone can change over time, resulting in increased or decreased cell sensitivity. In up-regulation, the number of receptors increases in response to rising hormone levels, making the cell more sensitive to the hormone and allowing for more cellular activity. When the number of receptors decreases in response to rising hormone levels, called down-regulation, cellular activity is reduced.

    Receptor binding alters cellular activity and results in an increase or decrease in normal body processes. Depending on the location of the protein receptor on the target cell and the chemical structure of the hormone, hormones can mediate changes directly by binding to intracellular hormone receptors and modulating gene transcription, or indirectly by binding to cell surface receptors and stimulating signaling pathways.

    Intracellular Hormone Receptors

    Lipid-derived (soluble) hormones can enter the cell by diffusing across the plasma membrane and binding to DNA to regulate gene transcription and to change the cell’s activities by inducing production of proteins that affect, in general, the long-term structure and function of the cell. Lipid insoluble hormones bind to receptors on the plasma membrane surface and trigger a signaling pathway to change the cell’s activities by inducing production of various cell products that affect the cell in the short-term. The hormone is called a first messenger and the cellular component is called a second messenger. G-proteins activate the second messenger (cyclic AMP), triggering the cellular response. Response to hormone binding is amplified as the signaling pathway progresses. Cellular responses to hormones include the production of proteins and enzymes and altered membrane permeability.