Anatomy and Physiology Chapter 3 Student Lecture Part 1

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by Emma Innis3 views·Updated Jun 8, 2024

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  1. All right. So this is my chapter three student lecture video
  2. and let's get started.
  3. First, we have intracellular and extracellular fluids.
  4. Extracellular is going to be outside of the cell.
  5. The cells are submersed in this fluid and it includes interstitial fluid,
  6. blood plasma cerebrospinal fluid and the extracellular matrix.
  7. The sodium concentration is high and the potassium concentration is low.
  8. Then we have intracellular which is inside of the cell.
  9. The intracellular fluid is made of cytosol.
  10. The sodium concentration is low and the potassium concentration is high
  11. following that. Um let's talk about the plasma membrane.
  12. So the plasma membrane is an active
  13. barrier that separates intracellular and extracellular fluid
  14. and it determines what can enter and leave the cell.
  15. So the plasma membrane is uh made of like a lipid bilayer
  16. with a water loving phosphate head
  17. which would be
  18. hydrophilic
  19. and water hating fatty acid tails which would be hydrophobic.
  20. There are also membrane proteins, lipids and carbohydrates.
  21. Um The possible membrane is semi permeable which
  22. means only certain things can pass through.
  23. So what can pass through the membrane?
  24. Only certain substances can easily pass through the plasma membrane,
  25. nonpolar substances uncharged and small
  26. um substances are the ones that can go through easily.
  27. But proteins can help determine whether or not a substance can enter the cell.
  28. So membrane proteins,
  29. there are two types of membrane proteins that
  30. can help determine what enters the cell.
  31. Many or
  32. membrane proteins have many functions.
  33. Integral proteins are embedded into the cell membrane
  34. and they have both hydrophobic and hydrophilic regions.
  35. They function as transport proteins, enzymes and receptors.
  36. But their most important function is transport.
  37. Then we have peripheral proteins which are loosely attached to integral proteins.
  38. And they include um filaments on the intracellular surface for
  39. membrane support
  40. and they function as enzymes and motor
  41. proteins.
  42. So functions of membrane proteins,
  43. they have many functions.
  44. So there's transport receptors for signal transduction, enzymatic activity,
  45. cell to cell joining
  46. cell to cell recognition
  47. and attachment to cyto
  48. skeleton and extracellular matrix.
  49. First transport
  50. proteins that span the membrane can create a hydrophilic
  51. channel that is selective for a particular solute.
  52. Some proteins break apart a TP with water that's called hydrolyzing
  53. and use it as energy to pump sub
  54. substances across the membrane. Like you can see on the picture to the right
  55. using a TP to get substances across the membrane is like an energetic currency.
  56. You kind of have to pay with a TP for something to be able to cross through.
  57. Then we have um receptors for signal transduction,
  58. a membrane protein on the outside of the cell may have
  59. a binding site that fits the shape of a chemical messenger.
  60. When connected
  61. the chemical may cause a change in the shape of the protein
  62. which can lead to a chain of chemical reactions within the cell.
  63. Only a certain type of molecule can attach and it has to be the correct shape.
  64. You can see to
  65. the right here
  66. that that little triangle fits perfectly within there.
  67. So that would be
  68. a binding site.
  69. Um
  70. Membrane receptor proteins serve as binding sites for chemical signals
  71. and they can contact signaling cells that
  72. they recognize on the cell surface.
  73. Some cells binding triggers enzyme activation.
  74. So maybe that little triangle going into that blue rectangle can
  75. signal activation
  76. lips.
  77. All right enzymatic activity.
  78. A membrane protein may be an enzyme with its
  79. active active site exposed in the adjacent solution.
  80. Several enzymes in a membrane can help catalyze steps.
  81. Enzymes are specific to what chemical reaction it wants to do.
  82. Each enzyme will complete a different chemical reaction.
  83. So, digestive enzymes will catalyze the hydrolysis of bonds and food molecules.
  84. So, since it is a digestive enzyme, that is its purpose, that is its function.
  85. All right cell to cell joining.
  86. So
  87. there are different kinds of ways that membrane proteins can
  88. connect. So there is tight junctions, desmosome and gap junctions.
  89. So we have gap junction
  90. off to the left of this photo. Here
  91. we have desma
  92. zone
  93. in the middle
  94. and we have tight junctions all the way to the right.
  95. So for tight junctions,
  96. the integral proteins on nearby cells will
  97. fuse and form an impermeable junction that
  98. uh
  99. encircles the whole cell.
  100. And it prevents most molecules from moving between cells.
  101. Desmosome are rivet like cell junctions formed with when linker proteins or C
  102. herons,
  103. um interlock like a zipper.
  104. The protein is anchored to the cell with a button like
  105. area on the inside of the plasma membrane called a plaque.
  106. And keratin filaments connect the plaques in intercellular
  107. for strength
  108. desmosome are give a little bit more, they are able to move more.
  109. So it reduces the possibility of tearing.
  110. Then gap junctions
  111. um have transmembrane proteins
  112. that form tunnels and they allow small molecules to pass from cell to cell
  113. cell to cell recognition.
  114. There are some glycoproteins that serve as name
  115. tags that are recognized by other cells.
  116. Um and proteins can tell which cells they are by this glycoprotein name tag
  117. and you can tell whether or not they're foreign
  118. or if they are supposed to be there.
  119. Lastly. Attachment to the cytoskeleton and extracellular matrix,
  120. the cytoskeleton and extracellular matrix will anchor to
  121. membrane proteins and this helps maintain cell shape
  122. and it fixes the location of membrane proteins and plays a role in cell movement.
  123. Next, we have diffusion and osmosis.
  124. So since the plasma membrane is semi permeable,
  125. only certain substances can pass through
  126. um substances can pass through using diffusion and osmosis
  127. diffusion and osmosis both fall under the category of passive transport,
  128. which means there is no energy used.
  129. Diffusion
  130. is the natural movement of molecules from areas
  131. of high concentration to areas of low concentration.
  132. There is passive transport,
  133. no energy and active transport uses energy.
  134. So this is an example of passive transport.
  135. As you can see in any of these photos, there is not um or any of the examples to the left,
  136. there is not being any A TP used,
  137. which would be our energetic currency like I talked about before.
  138. So there is simple diffusion where
  139. the molecules just pass through from
  140. uh one side to the other, no energy used.
  141. Then there is this channel
  142. that
  143. uh molecules are passing through no energy used.
  144. And then lastly, there's a carrier protein and there's not energy used.
  145. On the other side of the image,
  146. there is a TP being used in order for molecules to come through
  147. what affects diffusion.
  148. So concentration,
  149. the greater the difference of concentration between two areas,
  150. the faster a diffusion occurs
  151. molecule size. So smaller molecules diffuse faster
  152. and then temperature,
  153. higher temperatures can increase kinetic energy
  154. which results in faster diffusion.
  155. Molecules can move closer together when the heat is increased.
  156. All right. So
  157. facilitated diffusion.
  158. If something is preventing a molecule from crossing the
  159. membrane like being too large or too polar,
  160. it can use a protein or a channel to help it get through.
  161. Um facilitated, basically means that it needs assistance
  162. in order to pass through the membrane.
  163. And with that,
  164. um besides the carrier protein, there are also different types of channels
  165. that go along with that.
  166. So when using a protein, there's no energy use like I said before.
  167. But um
  168. certain hydrophobic molecules,
  169. for example,
  170. glucose amino acids and ions are
  171. transported possibly down their concentration gradient
  172. by carrier mediated facilitated diffusion.
  173. The molecule will attach to a protein and it will change
  174. its shape in order to help it move through the membrane
  175. binding of the molecule causes the carrier to envelop it
  176. like in this image down here to the right.
  177. And
  178. um
  179. it changes shape that allows the molecule to pass through.
  180. So, binding is also limited depending on how many carriers are present.
  181. Then we have channel mediated dis
  182. facilitated diffusion
  183. and that's what we'll move to. So there's different types of channels.
  184. So we have
  185. three different types of channels which are
  186. ligand
  187. gated channels which are closed at rest and open
  188. in response to binding of a specific chemical or
  189. ligand
  190. to a specific receptor.
  191. Then we have voltage gated channels that are closed at
  192. rest and respond to changes in voltage across the membrane.
  193. And then we have mechanically gated channels that are open
  194. and closed in response to mechanical stimulation
  195. such as pressure stretch or vibration.
  196. Next is osmosis.
  197. So osmosis is the movement of a solvent, usually water not molecules,
  198. osmolarity measures the concentration and of the total
  199. number of salute particles in a solvent.
  200. When salute concentration goes up, water concentration goes down and that
  201. is vice versa.
  202. Water moves by osmosis from areas of low
  203. salute concentration
  204. to high salute
  205. concentration.
  206. All right. So we have
  207. different types of pressures. So we have hydrostatic pressure,
  208. which is the outward pressure exerted on the cell side
  209. of the membrane
  210. caused by increases
  211. in volume of the cell due to osmosis
  212. osmosis.
  213. Then we have osmotic pressure
  214. which is inward pressure due to the tendency of water
  215. to be pulled into the cell with higher osmolarity.
  216. So more solvent in there.
  217. So back to hydrostatic, it's the pressure of water, water building up.
  218. Since the water wants to go from high concentration to low concentration
  219. for osmotic,
  220. um the more solutes inside the cell, the bigger pull on water to enter,
  221. resulting in a higher osmotic pressure inside the cell.
  222. Since the solvents want to go from high to low.
  223. All right, for tonicity.
  224. So,
  225. tonicity is the ability of a solution to change shape
  226. or tone of cells by altering the cells,
  227. internal water volume.
  228. So first we have an isotonic solution which is to the right of the image
  229. and it has the same osmolarity as the inside of the cell.
  230. The volume is not changed at all whatsoever.
  231. Then we have a hypertonic solution which is to the left of the image
  232. and it has a higher osmolarity than inside the cell.
  233. So water flows out of the cell resulting in shrinking
  234. or crenation.
  235. As you can see in the image,
  236. then we have
  237. a hypotonic solution that has a lower osmolarity than inside of the cell.
  238. So the water flows into the cell
  239. which causes the cell to swell
  240. and that could
  241. lead to cell bursting
  242. or lying.
  243. All right. So now on to active transport,
  244. there are two types of active transport.
  245. So there's active transport and vesicular transport. Both require a.