Cytoplasm & Organelles: The Cellular Level of Organization

Cytoplasm & Organelles

The Cellular Level of Organization

Part 2 HTHS 2110 Integrated Human Anatomy & Physiology I Unit 5

Objective 1: Cytoplasm, Cytosol, & Organelles

  • Cytoplasm = Cytosol + Organelles

    • Cytosol

    • Definition: The aqueous component of the cytoplasm in which organelles, proteins, and other cell structures are suspended.

      • Composed of:

      • Solvent: Water

      • Solutes:

        • Salts (e.g., Na, K, Cl)

        • Mono- & di-glycerides

        • Proteins (all dissolved in the matrix)

    • Organelles:

    • Definition: Specialized structures within a cell that perform specific functions, often referred to as "little organs."

    • Metaphor: Considered as the fruit pieces in a fruitcake, contributing to the overall function of the cell.


Objective 1: Organelles and Their Functions

Organelles Have a Job to Do

Organelle

Function

Objectives

Mitochondrion

Energy production

2, 6-8

Cytoskeleton

Structure

10

Cilia

Motility

11

Flagella

Motility

11

Ribosome

Protein synthesis

12

Rough endoplasmic reticulum

Synthesis

12

Smooth endoplasmic reticulum

Synthesis

12 (some types)

Golgi complex

Protein modification

Not specified

Spliceosome

RNA processing

Not specified

Lysosome

Storage & digestion

13

Peroxisome

Metabolic reactions

Not specified

Proteasome

Protein degradation

Not specified


Objective 2: Mitochondria

  • Mitochondria:

    • Definition: The energy-producing organelles in cells referred to as "ATP factories."

    • ATP (Adenosine triphosphate):

    • Definition: The energy currency of the cell, analogous to a rechargeable battery used for cellular processes.

    • Observations: Cells with higher energy needs possess a greater number of mitochondria, including:

    • Comparison: Muscle cells vs. skin cells

    • Comparison: Bone cells vs. nerve cells

    • Comparison: Red blood cells vs. white blood cells

    • Structure:

    • Composed of two phospholipid bilayers:

      • Outer membrane

      • Inner membrane: Extensively folded to increase surface area for energy generation.

    • Intermembrane space: Located between the outer and inner membranes.

    • Matrix: Area inside the inner membrane.

    • Genetic Material: Mitochondria contain their own DNA (mtDNA), which is maternally inherited (passed from mother to daughter or son).


Objective 3: Energy Chemical Reactions

  • Energy in Chemical Reactions

    • Activation energy is required to initiate chemical reactions.

    • Endergonic Reactions:

      • Type: Energy-absorbing (anabolic) reactions.

      • Requires energy input.

      • Direction: Absorbs energy into chemical bonds.

    • Exergonic Reactions:

      • Type: Energy-releasing (catabolic) reactions.

      • Performs work by releasing energy from chemical bonds.

      • Direction: Energy is released.

  • Significance of ATP:

    • Links anabolic (building) and catabolic (breaking down) processes.

      • Anabolic example: Formation of glycogen and proteins.

      • Catabolic example: Breakdown of glucose into simpler forms.

  • Burning vs. Metabolism:

    • Burning: Energy is released in one step (inefficient).

    • Metabolism: Energy is released in small, controlled steps, maximizing ATP capture as opposed to heat loss.


Objective 4: Cellular Respiration

  • Definition: The oxidation of glucose to produce ATP.

  • Overall Reaction:
    C6H{12}O6 + 6 O2
    ightarrow 6 CO2 + 6 H2O + 26-38 ATP

  • Four Main Steps:

    1. Glycolysis:

    • Location: Cytoplasm

    • Outcome: Splits glucose into two pyruvates, requiring 2 ATP and yielding 4 ATP (net gain of 2 ATP).

    1. Acetyl-CoA Formation:

    • Location: Mitochondrial matrix

    • Outcome: Converts pyruvic acid to acetyl-CoA, yielding 1 NADH + H+ and releasing 1 CO2 per pyruvate.

    1. Citric Acid Cycle:

    • Location: Mitochondrial matrix

    • Outcome: Each turn produces 2 CO2, 3 NADH + H+, 1 FADH2, and 1 ATP (per acetyl-CoA).

    1. Electron Transport Chain:

    • Location: Inner mitochondrial membrane

    • Function: NADH and FADH2 deliver protons and electrons, producing up to 30-34 ATP.


Objective 5: Glycolysis

  • Step 1 – Glycolysis:

    • In the cytosol, glucose is split during the energy investment phase, requiring 2 ATP.

    • Energy payoff phase produces 4 ATP (net gain of 2 ATP) and 2 pyruvic acids.

    • Products of Glycolysis:

      • Inputs: 1 glucose, 2 ATP, 2 NAD+, 2 inorganic phosphates.

      • Outputs: 4 ATP, 2 NADH, 2 pyruvate.


Objective 6: Formation of Acetyl Coenzyme A

  • Step 2 – Acetyl CoA Formation:

    • Occurs in mitochondrial matrix.

    • Reactants: Starts with pyruvic acid, requiring CoA and O2.

    • Products (per pyruvate):

    • 1 acetyl CoA

    • 1 CO2

    • 1 NADH + H+

    • Overall yield (per glucose):

    • 2 acetyl CoA

    • 2 CO2

    • 2 NADH + H+


Objective 7: The Citric Acid Cycle

  • Step 3 – Citric Acid Cycle:

    • Takes place in mitochondrial matrix.

    • Initiates with acetyl CoA and CoA is released.

    • Produces (per cycle):

    • 2 CO2

    • 3 NADH + H+

    • 1 FADH2

    • 1 ATP

    • Biological yield (per glucose):

    • 4 CO2

    • 6 NADH + H+

    • 2 FADH2

    • 2 ATP


Objective 8: The Electron Transport Chain

  • Occurs in inner mitochondrial membrane.

  • Mechanism:

    • NADH + H+ delivers protons and electrons which are separated in the electron transport chain.

    • Protons are pumped into the intermembrane space, creating a gradient that drives ATP production through ATP synthase.

  • Output: 22–34 ATP produced depending on efficiency.


Cellular Respiration Summary

  • Basic Process:

    • Glucose in cytosol → Glycolysis → Pyruvic acid → If O2 is present → Acetyl-CoA Formation → Citric Acid Cycle → Electron Transport Chain → Production of ATP.

  • Inefficiencies: Actual ATP yield is approximately 30-32 ATP per glucose.


Objective 9: Glycogen, Lipids, & Proteins as Energy Sources

  • Glycogen:

    • Long, branching chains of glucose, primarily stored in liver (70-100 g) and muscles (200-400 g).

    • Used for quick energy availability.

  • Lipids:

    • Excess glucose and fats can be stored as triglycerides.

    • Breakdown of triglycerides generates ketones and acids, which can lead to ketoacidosis.

  • Gluconeogenesis:

    • The process of creating new glucose from non-carbohydrate sources (fat or protein).


Objectives 10-13: Organelles

Meet the Organelles

Objective 10: Structural Organelles
  • Function: Provide cell structure and shape.

    • Examples: Cytoskeleton

Objective 11: Motility Organelles
  • Function: Move substances or the cell itself.

    • Examples: Cilia and Flagella

Objective 12: Synthesis Organelles
  • Function: Synthesize cell components.

    • Examples: Ribosomes, Rough ER

Objective 13: Storage & Digestion Organelles
  • Function: Store or break down materials.

    • Examples: Lysosomes, Peroxisomes, Proteasomes


Cytoskeleton Objective 10

  • Cytoskeleton: Provides structural stability and movement within cells.

  • Made up of different types of structural proteins:

    • Microfilaments (actin) - smallest (7 nm).

    • Intermediate filaments (keratin, vimentin) - medium size (8-12 nm).

    • Microtubules (tubulin) - largest (25 nm) involved in cell division and transport.


Cilia and Flagella

  • Cilia: Hair-like extensions on the cell surface that move fluids across the cell.

  • Flagella: Whip-like structures that move cells through fluid.

  • Structure: Both have a 9+2 arrangement of microtubules.

  • Function: Cilia use a rowing motion; flagella use a wave-like motion.


Ribosomes

  • Site of protein synthesis, made of large (60S) and small subunits (40S).

  • Function: Translate mRNA into proteins either attached to rough ER or as free ribosomes in the cytoplasm.


Endoplasmic Reticulum

  • Types:

    • Rough ER: Studded with ribosomes; synthesizes proteins for export.

    • Smooth ER: Functions in lipid synthesis, detoxification, and calcium storage.


Golgi Complex

  • Modifies, sorts, and packages proteins produced in rough ER.

  • Structure includes cis (entry face) and trans (exit face) regions.


Storage & Digestion Organelles

  • Lysosomes: Contain enzymes to break down waste and cellular debris, work best at an acid pH (5).

  • Peroxisomes: Contain enzymes to break down fatty acids and produce hydrogen peroxide which is further degraded.

  • Proteasomes: Responsible for degrading damaged or unneeded proteins with the help of ubiquitin.


Conclusion

  • The organelles and their functions are crucial for cellular homeostasis, energy production, and metabolism. Understanding these processes is fundamental for the study of human anatomy and physiology.