Alright. So here we're going to briefly revisit our map of the lesson on biosignalling pathways, which is down below right here. And of course, we know that we've been exploring this map by following the leftmost branches first. And already in our previous lesson videos, we've covered g-coupled protein receptors or GPCRs, and we've talked about all of these different branches in our previous lesson videos. And we've also talked about the receptor tyrosine kinases or RTKs. And we've covered the insulin and insulin receptor and talked about 2 different insulin RTK signaling pathways, one on glucose metabolism that included PI3K, PIP3, PKB, and PDK1, and another insulin RTK signaling pathway that was as a growth factor that included both the RAS pathway and the MAPK pathway. The RAS pathway, which included GRB2, SOS, and RAS, and the MAPK pathway, which included RAF1, MEK, and ERK. And we also discussed in our previous lesson videos a variation of an RTK, which was the JAK-STAT signaling pathway. And so now that we've covered all of the GPCRs and all of the RTKs that we're going to cover here in our course, we can finally move on to the final branch of our bio signaling map, which is over here, and we're going to discuss lipid hormone signaling. So let's get started with that. So here we're going to begin our introduction to lipid hormone signaling. And so recall from our previous lesson videos that hormones are really just defined as signaling molecules that are going to be released by a cell or gland that can travel and affect distant cells in other areas of the body. Now moving forward in our course, we're mainly going to talk about 2 main types of hormones, paracrine hormones and endocrine hormones. Now paracrine hormones are going to travel short distances, and only affect cells that are nearby in the vicinity of the synthesis of the paracrine hormone. Whereas, endocrine hormones, on the other hand, are released into the bloodstream, and we know that our bloodstream pretty much extends to all of the cells in our body. And so once endocrine hormones are released into the bloodstream, they could pretty much travel through the bloodstream long distances to their target cell. And so if we take a look at our image down below, notice that we're going to distinguish between, the top half of the image and the bottom half of the the image. And so the top half is showing us the paracrine hormones, and again the paracrine hormones are going to travel short distances, whereas the bottom half of the image down below is showing us the endocrine hormones, which again are going to travel long distances and affect target cells at a greater distance in different areas of the body. And so paracrine hormones, again, they travel short distances and only affect nearby cells in the area of their synthesis. And so notice over here on the left, we're showing you a signaling cell that's creating this green paracrine hormone here, and it's binding to the receptors on this specific target cell. And so the target cell is expressing the correct receptor to respond to the signals that the signaling cell is creating. This is going to elicit a bio signaling pathway in the target cell that leads to a cell response. But really the main difference here is paracrine hormones are traveling short distances here, affecting a neighboring target cell. Now if we take a look at the endocrine hormone down below the bottom half, again, it's going to travel long distances, and this is because the signaling cell that's creating the endocrine hormone is going to be, is going to be secreting the endocrine hormone into the bloodstream. And, of course, once it's in the bloodstream, it can diffuse long, long distances to completely different areas of the body and affect target cells in different areas of the body. And so here we have a target cell that's expressing the correct receptor here to respond to the endocrine hormone, and that's going to elicit a bio signalling pathway in the target cell that leads to a cell response. But, again, the main difference here is paracrine hormones travel short distances, whereas endocrine hormones travel long distances because they are secreted into the bloodstream. And so this here concludes our introduction to hormones, specifically paracrine and endocrine hormones. And as we move along in our course, we'll be able to talk more and more about lipid hormone signaling. And so I'll see you guys in our next video.
- 1. Introduction to Biochemistry4h 34m
- What is Biochemistry?5m
- Characteristics of Life12m
- Abiogenesis13m
- Nucleic Acids16m
- Proteins12m
- Carbohydrates8m
- Lipids10m
- Taxonomy10m
- Cell Organelles12m
- Endosymbiotic Theory11m
- Central Dogma22m
- Functional Groups15m
- Chemical Bonds13m
- Organic Chemistry31m
- Entropy17m
- Second Law of Thermodynamics11m
- Equilibrium Constant10m
- Gibbs Free Energy37m
- 2. Water3h 23m
- 3. Amino Acids8h 10m
- Amino Acid Groups8m
- Amino Acid Three Letter Code13m
- Amino Acid One Letter Code37m
- Amino Acid Configuration20m
- Essential Amino Acids14m
- Nonpolar Amino Acids21m
- Aromatic Amino Acids14m
- Polar Amino Acids16m
- Charged Amino Acids40m
- How to Memorize Amino Acids1h 7m
- Zwitterion33m
- Non-Ionizable Vs. Ionizable R-Groups11m
- Isoelectric Point10m
- Isoelectric Point of Amino Acids with Ionizable R-Groups51m
- Titrations of Amino Acids with Non-Ionizable R-Groups44m
- Titrations of Amino Acids with Ionizable R-Groups38m
- Amino Acids and Henderson-Hasselbalch44m
- 4. Protein Structure10h 4m
- Peptide Bond18m
- Primary Structure of Protein31m
- Altering Primary Protein Structure15m
- Drawing a Peptide44m
- Determining Net Charge of a Peptide42m
- Isoelectric Point of a Peptide37m
- Approximating Protein Mass7m
- Peptide Group22m
- Ramachandran Plot26m
- Atypical Ramachandran Plots12m
- Alpha Helix15m
- Alpha Helix Pitch and Rise20m
- Alpha Helix Hydrogen Bonding24m
- Alpha Helix Disruption23m
- Beta Strand12m
- Beta Sheet12m
- Antiparallel and Parallel Beta Sheets39m
- Beta Turns26m
- Tertiary Structure of Protein16m
- Protein Motifs and Domains23m
- Denaturation14m
- Anfinsen Experiment20m
- Protein Folding34m
- Chaperone Proteins19m
- Prions4m
- Quaternary Structure15m
- Simple Vs. Conjugated Proteins10m
- Fibrous and Globular Proteins11m
- 5. Protein Techniques14h 5m
- Protein Purification7m
- Protein Extraction5m
- Differential Centrifugation15m
- Salting Out18m
- Dialysis9m
- Column Chromatography11m
- Ion-Exchange Chromatography35m
- Anion-Exchange Chromatography38m
- Size Exclusion Chromatography28m
- Affinity Chromatography16m
- Specific Activity16m
- HPLC29m
- Spectrophotometry51m
- Native Gel Electrophoresis23m
- SDS-PAGE34m
- SDS-PAGE Strategies16m
- Isoelectric Focusing17m
- 2D-Electrophoresis23m
- Diagonal Electrophoresis29m
- Mass Spectrometry12m
- Mass Spectrum47m
- Tandem Mass Spectrometry16m
- Peptide Mass Fingerprinting16m
- Overview of Direct Protein Sequencing30m
- Amino Acid Hydrolysis10m
- FDNB26m
- Chemical Cleavage of Bonds29m
- Peptidases1h 6m
- Edman Degradation30m
- Edman Degradation Sequenator and Sequencing Data Analysis4m
- Edman Degradation Reaction Efficiency20m
- Ordering Cleaved Fragments21m
- Strategy for Ordering Cleaved Fragments58m
- Indirect Protein Sequencing Via Geneomic Analyses24m
- 6. Enzymes and Enzyme Kinetics13h 38m
- Enzymes24m
- Enzyme-Substrate Complex17m
- Lock and Key Vs. Induced Fit Models23m
- Optimal Enzyme Conditions9m
- Activation Energy24m
- Types of Enzymes41m
- Cofactor15m
- Catalysis19m
- Electrostatic and Metal Ion Catalysis11m
- Covalent Catalysis18m
- Reaction Rate10m
- Enzyme Kinetics24m
- Rate Constants and Rate Law35m
- Reaction Orders52m
- Rate Constant Units11m
- Initial Velocity31m
- Vmax Enzyme27m
- Km Enzyme42m
- Steady-State Conditions25m
- Michaelis-Menten Assumptions18m
- Michaelis-Menten Equation52m
- Lineweaver-Burk Plot43m
- Michaelis-Menten vs. Lineweaver-Burk Plots20m
- Shifting Lineweaver-Burk Plots37m
- Calculating Vmax40m
- Calculating Km31m
- Kcat46m
- Specificity Constant1h 1m
- 7. Enzyme Inhibition and Regulation 8h 42m
- Enzyme Inhibition13m
- Irreversible Inhibition12m
- Reversible Inhibition9m
- Inhibition Constant26m
- Degree of Inhibition15m
- Apparent Km and Vmax29m
- Inhibition Effects on Reaction Rate10m
- Competitive Inhibition52m
- Uncompetitive Inhibition33m
- Mixed Inhibition40m
- Noncompetitive Inhibition26m
- Recap of Reversible Inhibition37m
- Allosteric Regulation7m
- Allosteric Kinetics17m
- Allosteric Enzyme Conformations33m
- Allosteric Effectors18m
- Concerted (MWC) Model25m
- Sequential (KNF) Model20m
- Negative Feedback13m
- Positive Feedback15m
- Post Translational Modification14m
- Ubiquitination19m
- Phosphorylation16m
- Zymogens13m
- 8. Protein Function 9h 41m
- Introduction to Protein-Ligand Interactions15m
- Protein-Ligand Equilibrium Constants22m
- Protein-Ligand Fractional Saturation32m
- Myoglobin vs. Hemoglobin27m
- Heme Prosthetic Group31m
- Hemoglobin Cooperativity23m
- Hill Equation21m
- Hill Plot42m
- Hemoglobin Binding in Tissues & Lungs31m
- Hemoglobin Carbonation & Protonation19m
- Bohr Effect23m
- BPG Regulation of Hemoglobin24m
- Fetal Hemoglobin6m
- Sickle Cell Anemia24m
- Chymotrypsin18m
- Chymotrypsin's Catalytic Mechanism38m
- Glycogen Phosphorylase21m
- Liver vs Muscle Glycogen Phosphorylase21m
- Antibody35m
- ELISA15m
- Motor Proteins14m
- Skeletal Muscle Anatomy22m
- Skeletal Muscle Contraction45m
- 9. Carbohydrates7h 49m
- Carbohydrates19m
- Monosaccharides15m
- Stereochemistry of Monosaccharides33m
- Monosaccharide Configurations32m
- Cyclic Monosaccharides20m
- Hemiacetal vs. Hemiketal19m
- Anomer14m
- Mutarotation13m
- Pyranose Conformations23m
- Common Monosaccharides33m
- Derivatives of Monosaccharides21m
- Reducing Sugars21m
- Reducing Sugars Tests19m
- Glycosidic Bond48m
- Disaccharides40m
- Glycoconjugates12m
- Polysaccharide7m
- Cellulose7m
- Chitin8m
- Peptidoglycan12m
- Starch13m
- Glycogen14m
- Lectins16m
- 10. Lipids5h 49m
- Lipids15m
- Fatty Acids30m
- Fatty Acid Nomenclature11m
- Omega-3 Fatty Acids12m
- Triacylglycerols11m
- Glycerophospholipids24m
- Sphingolipids13m
- Sphingophospholipids8m
- Sphingoglycolipids12m
- Sphingolipid Recap22m
- Waxes5m
- Eicosanoids19m
- Isoprenoids9m
- Steroids14m
- Steroid Hormones11m
- Lipid Vitamins19m
- Comprehensive Final Lipid Map13m
- Biological Membranes16m
- Physical Properties of Biological Membranes18m
- Types of Membrane Proteins8m
- Integral Membrane Proteins16m
- Peripheral Membrane Proteins12m
- Lipid-Linked Membrane Proteins21m
- 11. Biological Membranes and Transport 6h 37m
- Biological Membrane Transport21m
- Passive vs. Active Transport18m
- Passive Membrane Transport21m
- Facilitated Diffusion8m
- Erythrocyte Facilitated Transporter Models30m
- Membrane Transport of Ions29m
- Primary Active Membrane Transport15m
- Sodium-Potassium Ion Pump20m
- SERCA: Calcium Ion Pump10m
- ABC Transporters12m
- Secondary Active Membrane Transport12m
- Glucose Active Symporter Model19m
- Endocytosis & Exocytosis18m
- Neurotransmitter Release23m
- Summary of Membrane Transport21m
- Thermodynamics of Membrane Diffusion: Uncharged Molecule51m
- Thermodynamics of Membrane Diffusion: Charged Ion1h 1m
- 12. Biosignaling9h 45m
- Introduction to Biosignaling44m
- G protein-Coupled Receptors32m
- Stimulatory Adenylate Cyclase GPCR Signaling42m
- cAMP & PKA28m
- Inhibitory Adenylate Cyclase GPCR Signaling29m
- Drugs & Toxins Affecting GPCR Signaling20m
- Recap of Adenylate Cyclase GPCR Signaling5m
- Phosphoinositide GPCR Signaling58m
- PSP Secondary Messengers & PKC27m
- Recap of Phosphoinositide Signaling7m
- Receptor Tyrosine Kinases26m
- Insulin28m
- Insulin Receptor23m
- Insulin Signaling on Glucose Metabolism57m
- Recap Of Insulin Signaling in Glucose Metabolism6m
- Insulin Signaling as a Growth Factor1h 1m
- Recap of Insulin Signaling As A Growth Factor9m
- Recap of Insulin Signaling1m
- Jak-Stat Signaling25m
- Lipid Hormone Signaling15m
- Summary of Biosignaling13m
- Signaling Defects & Cancer20m
- Review 1: Nucleic Acids, Lipids, & Membranes2h 47m
- Nucleic Acids 19m
- Nucleic Acids 211m
- Nucleic Acids 34m
- Nucleic Acids 44m
- DNA Sequencing 19m
- DNA Sequencing 211m
- Lipids 111m
- Lipids 24m
- Membrane Structure 110m
- Membrane Structure 29m
- Membrane Transport 18m
- Membrane Transport 24m
- Membrane Transport 36m
- Practice - Nucleic Acids 111m
- Practice - Nucleic Acids 23m
- Practice - Nucleic Acids 39m
- Lipids11m
- Practice - Membrane Structure 17m
- Practice - Membrane Structure 25m
- Practice - Membrane Transport 16m
- Practice - Membrane Transport 26m
- Review 2: Biosignaling, Glycolysis, Gluconeogenesis, & PP-Pathway3h 12m
- Biosignaling 19m
- Biosignaling 219m
- Biosignaling 311m
- Biosignaling 49m
- Glycolysis 17m
- Glycolysis 27m
- Glycolysis 38m
- Glycolysis 410m
- Fermentation6m
- Gluconeogenesis 18m
- Gluconeogenesis 27m
- Pentose Phosphate Pathway15m
- Practice - Biosignaling13m
- Practice - Bioenergetics 110m
- Practice - Bioenergetics 216m
- Practice - Glycolysis 111m
- Practice - Glycolysis 27m
- Practice - Gluconeogenesis5m
- Practice - Pentose Phosphate Path6m
- Review 3: Pyruvate & Fatty Acid Oxidation, Citric Acid Cycle, & Glycogen Metabolism2h 26m
- Pyruvate Oxidation9m
- Citric Acid Cycle 114m
- Citric Acid Cycle 27m
- Citric Acid Cycle 37m
- Citric Acid Cycle 411m
- Metabolic Regulation 18m
- Metabolic Regulation 213m
- Glycogen Metabolism 16m
- Glycogen Metabolism 28m
- Fatty Acid Oxidation 111m
- Fatty Acid Oxidation 28m
- Citric Acid Cycle Practice 17m
- Citric Acid Cycle Practice 26m
- Citric Acid Cycle Practice 32m
- Glucose and Glycogen Regulation Practice 14m
- Glucose and Glycogen Regulation Practice 26m
- Fatty Acid Oxidation Practice 14m
- Fatty Acid Oxidation Practice 27m
- Review 4: Amino Acid Oxidation, Oxidative Phosphorylation, & Photophosphorylation1h 48m
- Amino Acid Oxidation 15m
- Amino Acid Oxidation 211m
- Oxidative Phosphorylation 18m
- Oxidative Phosphorylation 210m
- Oxidative Phosphorylation 310m
- Oxidative Phosphorylation 47m
- Photophosphorylation 15m
- Photophosphorylation 29m
- Photophosphorylation 310m
- Practice: Amino Acid Oxidation 12m
- Practice: Amino Acid Oxidation 22m
- Practice: Oxidative Phosphorylation 15m
- Practice: Oxidative Phosphorylation 24m
- Practice: Oxidative Phosphorylation 35m
- Practice: Photophosphorylation 15m
- Practice: Photophosphorylation 21m
Lipid Hormone Signaling: Study with Video Lessons, Practice Problems & Examples
Biosignaling pathways involve various hormones, primarily categorized as paracrine and endocrine. Paracrine hormones act locally, affecting nearby cells, while endocrine hormones travel long distances through the bloodstream to reach target cells. Lipid hormones, such as steroids derived from cholesterol, can diffuse through plasma membranes and bind to intracellular receptors, influencing metabolic responses and gene expression. In contrast, non-lipid hormones bind to extracellular receptors, necessitating signal transduction for their effects. Understanding these mechanisms is crucial for grasping cellular communication and response.
Lipid Hormone Signaling
Video transcript
What is the major difference between paracrine and endocrine signaling?
Upon secretion, a chemical messenger (hormone) binds its receptors on other cells that were nearby. The hormone was secreted in such low concentration that it did not have any effect on distant cells, even though those distant cells had the appropriate receptors. We would best classify this hormone as a(n):
Lipid Hormone Signaling
Video transcript
So here in this video, we're going to continue to talk about lipid hormone signaling. More specifically, we're going to focus on how lipid hormones are capable of diffusing straight through the plasma membrane. Now what's important to note is that most hormones are either proteins such as insulin, amino acid derivatives such as epinephrine, or steroids such as estrogen. And so recall that way back in some of our previous lesson videos, we actually did cover steroid hormones when we talked about lipids, and so we know that these steroid hormones are really just defined as these hydrophobic molecules that are derived from cholesterol. Now the hydrophobic nature of these lipid steroid hormones is really really important because this allows lipid hormones to commonly bind to intracellular receptors. And these intracellular receptors are going to be found on the inside of cells, either in the cytoplasm or in the nucleus. And this is very, very different from the non-lipid hormones that we talked about in our previous lesson videos, because non-lipid hormones don't really have this hydrophobic nature, and so they are going to bind exclusively to extracellular portions of receptors in the plasma membrane. And so if we take a look at our image down below, notice that the non-lipid hormones that we talked about in our previous lesson videos, such as Epinephrine and Insulin, are going to bind specifically to the extracellular portions of receptors that are embedded in the cell's plasma membrane. But the non-lipid hormones are not capable of diffusing directly through the plasma membrane or into the nuclear membrane. And again, that's because the nature of non-lipid hormones is not really hydrophobic enough to allow them to diffuse directly through plasma membranes. However, when it comes to lipid hormones on the other hand such as estrogen, notice that they are capable of diffusing directly through the plasma membrane to have a direct effect on the metabolic response, or they could diffuse through the plasma membrane and through the nuclear membrane to have a direct effect on gene expression responses. Whereas again, the non-lipid hormones have to bind to the extracellular portions and they have to go through signal transduction in order to have their effect on metabolic response or gene expression. And so, notice that some lipid hormones, can also have the capability of binding to extracellular portions of receptors as well, and they can also lead to signal transduction in some cases as well that leads to metabolic responses or gene expression responses. But, you can see how lipid hormones can be diverse. They can bind to extracellular portions. They can diffuse directly through the plasma membrane, or they can diffuse through the plasma membrane and through the nuclear membrane. And so a scientist or a researcher needs to be really, really aware of the type of hormone that they're working with. Because if they're working with non-lipid hormones, then they know for sure that they're going to bind to extracellular portions of receptors. But if they're working with lipid hormones, then they need to be aware that lipid hormones are capable of either binding to extracellular portions of receptors, but they're also capable of diffusing directly through plasma membranes and nuclear membranes as well to have a more direct effect on metabolic response and gene expression responses. And so this here concludes our lesson on how lipid hormones have the ability to diffuse through plasma membranes unlike non-lipid hormones. And so we'll be able to get some practice applying these concepts as we move forward in our course, so I'll see you guys in our next video.
The main difference between hormones that have intracellular receptors and those that have cell membrane receptors is that the former tend to be _______:
a) Larger.
b) Charged.
c) Amino acid derivatives.
d) Proteins.
e) Hydrophobic.
Here’s what students ask on this topic:
What are the main differences between paracrine and endocrine hormones?
Paracrine hormones act locally, affecting nearby cells in the vicinity of their synthesis. They travel short distances and bind to receptors on neighboring target cells. In contrast, endocrine hormones are released into the bloodstream, allowing them to travel long distances to reach target cells in different areas of the body. This distinction is crucial for understanding how different hormones coordinate various physiological processes. Paracrine signaling is typically involved in localized responses, while endocrine signaling can regulate functions throughout the entire organism.
How do lipid hormones differ from non-lipid hormones in their mechanism of action?
Lipid hormones, such as steroids derived from cholesterol, are hydrophobic and can diffuse directly through the plasma membrane. They often bind to intracellular receptors located in the cytoplasm or nucleus, directly influencing metabolic responses and gene expression. Non-lipid hormones, like proteins and amino acid derivatives, are hydrophilic and cannot pass through the plasma membrane. Instead, they bind to extracellular receptors, initiating a signal transduction pathway to exert their effects. This fundamental difference in mechanism highlights the diverse ways hormones can regulate cellular functions.
Why can lipid hormones diffuse through the plasma membrane while non-lipid hormones cannot?
Lipid hormones are hydrophobic molecules, allowing them to easily diffuse through the lipid bilayer of the plasma membrane. This property enables them to enter cells and interact with intracellular receptors. Non-lipid hormones, on the other hand, are hydrophilic and cannot penetrate the hydrophobic core of the plasma membrane. Therefore, they must bind to extracellular receptors to initiate a signal transduction cascade that transmits the signal into the cell. This difference in permeability is due to the distinct chemical nature of lipid versus non-lipid hormones.
What roles do intracellular receptors play in lipid hormone signaling?
Intracellular receptors are crucial for lipid hormone signaling. These receptors are located either in the cytoplasm or the nucleus of target cells. When lipid hormones, such as steroids, diffuse through the plasma membrane, they bind to these intracellular receptors. This binding often results in the hormone-receptor complex translocating to the nucleus, where it can directly influence gene expression by acting as a transcription factor. This mechanism allows lipid hormones to exert a direct and potent effect on cellular functions, including metabolism and growth.
How do paracrine and endocrine hormones contribute to biosignaling pathways?
Paracrine and endocrine hormones are integral to biosignaling pathways. Paracrine hormones act locally, affecting nearby cells and facilitating rapid, localized responses. This is essential for processes like inflammation and tissue repair. Endocrine hormones, released into the bloodstream, can travel throughout the body to regulate distant target cells. This long-range signaling is vital for maintaining homeostasis, growth, and development. Together, these hormones ensure that cells can communicate effectively, coordinating complex physiological processes across different scales and distances within the organism.