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Lesson 1: Cell Biology

Learning Objectives

  • Identify the structural parts of a typical human (eukaryotic) cell.
  • Describe the core functions each structure (organelle, membrane, fluid, etc.) performs for overall body health.
  • Build conceptual foundations that will later clarify microbiology, immunology and genetics sections.

Course & Reading Context

  • Support text: Tortora, Principles of Anatomy and Physiology 3^{\text{rd}} edition (ebook via Massey Library).
  • Related paper: 214.101 Normal Body Function.

Big-Picture Definitions

TermMeaningKey Analogies/Notes
Cell (Eukaryotic)Basic living structural & functional unit of humans.Cartoon cell “sliced in half” lets us see the “guts.”
Cell BiologyStudy of the structure & function of cells.“Why I’m banging on about this crazy stuff.”
OrganelleMembrane-bound “little organs” inside cytoplasm.Each plays a specialised role a bit like departments in a factory.
Cellular DifferentiationGenetic programming that produces different shapes, sizes, organelle counts (skin vs. heart vs. gut vs. neuron).Driven by DNA during development.

Ethical/Clinical relevance: Understanding “normal” empowers recognition of pathologies (e.g., lysosomal storage diseases, immune defects) and appreciation of microbial diversity.


Three Main Structural Regions

  1. Plasma (Cell) Membrane
  2. Cytoplasm (cytosol + suspended organelles)
  3. Nucleus

Plasma Membrane ― “Double-Glazing”

  • Composition: Lipid bilayer (two parallel rows of phospholipids).
  • Functions
    • Maintains cell’s shape & integrity.
    • Selectively controls molecular traffic via integral proteins, channels & receptors.
    • Specialised immune cells (e.g.
    • Neutrophils / Macrophages use surface pattern-recognition receptors to bind microbes → engulf by phagocytosis ("vacuum cleaner" analogy).
  • Health link: Membrane defects = leakage, auto-immune issues, impaired signalling.

Cytoplasm

  • Mostly water, dissolved salts, nutrients.
  • Suspension medium for organelles.
  • Dynamic staging ground for countless metabolic pathways.

Ribosomes ― “Protein Factories”

  • Tiny 2-subunit machines (large + small) made primarily of ribosomal RNA (rRNA).
  • Two locations
    • Free in cytosol → create proteins used inside the cell.
    • Bound to Rough ER → translate proteins destined for secretion, membranes or organelles.
  • Process: mRNA thread enters → amino acid chain exits (protein synthesis).

Examples of protein output

  • Steroid-converting enzymes, mucus constituents, immunoglobulins, “snot,” etc.

Endoplasmic Reticulum (ER)

Overall Layout

Outer extension of the nuclear envelope; labyrinthine tubes & sacs.

Rough ER (RER)

  • "Rough" = studded with ribosomes (push-pin imagery).
  • Core role: cotranslational protein synthesis + early folding/quality control.

Smooth ER (SER)

  • Lacks ribosomes → smooth look.
  • Functions
    • Synthesises lipids, phospholipids, steroid hormones.
    • Regulates intracellular Ca^{2+} — vital for muscle contraction & cardiac rhythm.

Mnemonic: Rough = Ribosomes & pRoteins; Smooth = Steroids & Salts (Ca^{2+}).


Golgi Complex ― “Courier Centre / Post Office”

  • Stack of flattened sacs (resembles ER cross-section but sits deeper in cytoplasm, not continuous with nucleus).
  • Cis face (receiving): accepts new proteins from RER.
  • Intrinsic enzymes modify, sort & label cargo.
  • Trans face (shipping): dispatches finished vesicles to
    1. Cell surface for secretion (e.g.
      hormones, mucus).
    2. Plasma membrane insertion.
    3. Lysosomes for degradation if faulty.

Process = receive → package → address → ship (two-sided workflow).


Lysosomes ― “Jaffas / Rubbish Dumps”

  • Spherical vesicles packed with hydrolytic enzymes (low pH interior).
  • Jobs
    • Digest obsolete organelles, mis-folded proteins (autophagy).
    • Fuse with phagosomes in immune cells to kill microbes (autolysis if ruptured).
  • Clinical tie-ins
    • Inherited lysosomal storage diseases (enzymatic defects) → toxic buildup → often fatal.
    • Analogy: city garbage workers strike → rubbish overflows, chaos ensues.

Vesicular Traffic Map (Integration Diagram)

  1. DNA in nucleus → transcribed to mRNA.
  2. mRNA exits nuclear pore → joins ribosome.
  3. Protein made, enters RER lumen.
  4. Budding transport vesicles carry to Golgi.
  5. Golgi sorts →
    • Secretion vesicle → plasma membrane.
    • Membrane vesicle → becomes new membrane patch.
    • Mistake/faulty cargo → lysosome for destruction.
  6. External materials entering by endocytosis may merge directly with lysosomes for disassembly.

Mitochondria ― “Bean-Shaped Power Plants”

  • Double membrane; inner membrane forms extensive cristae (pastry-style folds) → massive surface area.
  • Perform aerobic respiration: glucose + O2 → CO2 + H_2O + ATP (adenosine triphosphate) — universal energy currency.
  • Evolutionary note
    • Descended from engulfed bacteria (endosymbiotic theory).
    • Possess circular mitochondrial DNA; inherited maternally.
  • Pathophysiology: Mitochondrial mutations → metabolic syndromes, neuro-muscular diseases.

Surface Projections

Cilia ― “Moving Carpets of Hair”

  • Short, numerous; beat in coordinated wave.
  • Line respiratory tract, sinuses, parts of reproductive & digestive systems.
  • Function: propel mucus (laden with immunoglobulins, debris, microbes) outwards → prevents infection & blockage.
  • Dysfunction (e.g.
    Primary Ciliary Dyskinesia) → chronic respiratory issues, infertility.

Flagella ― “Turbo Tails”

  • Long, usually singular; whip-like rotation due to microtubule motor proteins.
  • Human example: sperm flagellum drives long-distance journey to ovum.

Nucleus ― “Headquarters / Library”

  • Wrapped by nuclear envelope with protein-rich nuclear pores for traffic control.
  • Chromatin = DNA + histone proteins; appears tangled when cell not dividing.
  • Nucleolus (ignored for now) = ribosome subunit factory.
  • Major flows
    1. Transcription: DNA → mRNA → exits pore.
    2. Regulatory proteins & raw materials travel in.
  • During mitosis: chromatin condenses into visible chromosomes (detailed later).

Summary Diagram & Study Tips

  • Core organelles: Nucleus, Ribosomes, RER, SER, Golgi, Lysosomes, Mitochondria, Plasma Membrane, Cilia/Flagella.
  • Visual learners: red-raw annotated cell cartoons or 3-D apps.
  • Verbal learners: summary tables (as on Stream) with two-column “Organelle | Function.”
  • Link to medicine: every pathology (inflammation, cancer, infection, genetic disease) can be traced to malfunctions in one or more of these systems.

Key Analogies & Metaphors Recap

  • Plasma membrane = “double-glazing” or “double rainbow.”
  • Phagocytic immune cell = “vacuum cleaner.”
  • Ribosome subunits = “clip together like LEGO.”
  • Rough vs. Smooth ER = “nail file” (coarse vs. fine sides).
  • Golgi = “courier centre/post office.”
  • Lysosome = “Jaffa” full of acid → garbage dump/car-wash for pathogens.
  • Mitochondrion = “folded pastry bean” fueled by Red Bull moment.
  • Cilia movement = “wave dance.”

Practical / Clinical Connections

  1. Immune defence: phagocytosis + lysosome fusion.
  2. Hormone secretion: RER → Golgi → exocytosis.
  3. Muscle & heart physiology: SER Ca^{2+} handling; mitochondrial ATP supply.
  4. Genetic disorders: lysosomal storage, mitochondrial myopathies, ciliary dyskinesia.
  5. Pharmacology: many drugs target membrane receptors, ribosomes (antibiotics vs. bacteria), mitochondrial metabolism (chemotherapy), etc.

Final Checklist for Self-Assessment

  • Can I sketch a cell and label at least 8 organelles?
  • Can I match each organelle to its primary function in one sentence?
  • Do I understand how ER, Golgi and lysosomes form a dynamic logistic chain?
  • Can I explain why mitochondria have their own DNA and why that matters clinically?
  • Can I relate ciliary motion to airway hygiene and flagellar motion to fertility?

If any box remains unchecked, re-read corresponding section or visualise the analogies until the concept sticks.