Cell Biology and Organelles

Cell Biology and Organelles

Cell Biology and Organelles

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Cell Membrane & Transport - Border Patrol Gates

Fluid mosaic model of cell membrane

  • Structure: Fluid mosaic model. Amphipathic phospholipid bilayer; cholesterol (fluidity buffer). Proteins: integral (transmembrane channels, carriers, pumps), peripheral (enzymes, receptors). Glycocalyx (carbohydrate coat; cell ID, protection, adhesion).

  • Transport Mechanisms:

  • Key Players:

    • Na+/K+ Pump: 3 Na+ out, 2 K+ in per ATP. Vital for gradients.
    • GLUTs: Facilitated glucose entry (e.g., GLUT2 in liver, pancreas; GLUT4 insulin-dependent).

    ⭐ SGLT1 (kidney/intestine) & SGLT2 (kidney) are Na+-glucose cotransporters targeted by SGLT2 inhibitors (gliflozins).

  • Bulk Transport: Endocytosis (phagocytosis, pinocytosis, receptor-mediated), Exocytosis (secretion).

Cytoskeleton & Junctions - Cell's Inner Framework

Cytosol: Fluid matrix; Inclusions: Glycogen, lipids.

  • Microfilaments (Actin): Cell shape, motility, muscle contraction.
  • Intermediate Filaments (IFs): Support. Types: Keratin (epith), Vimentin (mesench), Desmin (musc), GFAP (glia), Lamins (nucl). Diagnostic.
  • Microtubules (Tubulin): Cilia, flagella, mitotic spindle. Drug targets: Colchicine, Vinca alkaloids, Taxanes. Types of cell junctions

Cell Junctions:

TypeKey ProteinsMain Function
Tight (Occludens)Occludins, ClaudinsSeals intercellular space
AdherensCadherins (E-cadherin)Links actin; cell-cell adhesion
DesmosomeCadherins (Desmoglein)Links IFs; strong adhesion
GapConnexinsDirect cell-cell communication
HemidesmosomeIntegrinsLinks IFs to basal lamina

Endomembrane System - Protein Factory Mail

  • Nucleus: Double envelope with pores; nucleolus (rRNA synthesis); chromatin (euchromatin-active, heterochromatin-condensed).
  • Rough ER (RER): Studded with ribosomes; synthesizes proteins for secretion/organelles, N-glycosylation.
  • Smooth ER (SER): Lipid/steroid synthesis, detoxification, Ca2+ storage (sarcoplasmic reticulum in muscle).
  • Golgi Apparatus: Cis→Medial→Trans. Modifies (e.g., O-glycosylation), sorts, packages proteins. Vesicles: COP-II (ER→Golgi), COP-I (Golgi→ER).
  • Lysosomes: Contain acid hydrolases (pH ~5). Functions: autophagy, crinophagy. Storage diseases (e.g., Tay-Sachs, Gaucher).

image

⭐ Mannose-6-phosphate (M6P) targets enzymes to lysosomes. Defect causes I-cell disease (Mucolipidosis II).

Mitochondria & Peroxisomes - Power Plant Cleaners

  • Mitochondria (Cell's Powerhouse)
    • Structure: Double membrane; inner folded into cristae (↑ surface area for ATP synthesis). Matrix: Krebs cycle enzymes.
    • Energy: ATP synthesis via oxidative phosphorylation (ETC on inner membrane).
    • Genetics: Own circular mtDNA, maternally inherited. Mitochondria and Peroxisomes Ultrastructure
  • Peroxisomes (Detox & Lipid Hub)
    • Functions:
      • Oxidases (produce $H_2O_2$) & catalase (degrades $H_2O_2$).
      • β-oxidation of Very Long Chain Fatty Acids (VLCFA).
      • Plasmalogen synthesis (ether phospholipids for myelin).
      • Detoxification.
    • Disorders:

      ⭐ Zellweger Syndrome: Autosomal recessive; absent/empty peroxisomes cause severe neurological issues.

Cell Cycle & Division - Duplication Dance Drama

  • Phases: Interphase (G1-growth, S-DNA replication, G2-prep for M); M-phase (Mitosis/Meiosis). 📌 G1→S→G2→M.
  • Regulation: Cyclins & CDKs drive progression. Tumor suppressors: p53 (genome guardian), Rb (G1/S checkpoint).
  • Checkpoints: G1/S (restriction), G2/M (DNA integrity), Spindle assembly (metaphase).
  • Mitosis: PMAT stages → 2 identical diploid (2n) cells. For somatic cell proliferation.
  • Meiosis: Meiosis I & II → 4 unique haploid (n) gametes; genetic recombination (Prophase I).
  • Cell Death: Apoptosis (programmed, caspases via intrinsic/extrinsic pathways, non-inflammatory) vs. Necrosis (pathological, inflammatory).

⭐ p53 gene mutations are found in over 50% of human cancers, highlighting its critical role.

Cell Cycle Checkpoints and Regulatory Proteins

High‑Yield Points - ⚡ Biggest Takeaways

  • Mitochondria: ATP synthesis (oxidative phosphorylation), double membrane, maternal inheritance.
  • RER: Ribosome-studded; synthesis & modification of secretory/membrane proteins.
  • SER: Lipid & steroid synthesis, detoxification, Ca2+ storage.
  • Golgi Apparatus: Protein/lipid modification, sorting, packaging for delivery.
  • Lysosomes: Acid hydrolases for degradation; defects lead to storage diseases (e.g., Tay-Sachs).
  • Peroxisomes: VLCFA beta-oxidation, detoxification (H2O2 metabolism).
  • Nucleolus: Site of rRNA synthesis and ribosome assembly.

Practice Questions: Cell Biology and Organelles

Test your understanding with these related questions

Which of the following statements regarding collagen synthesis is incorrect?

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Flashcards: Cell Biology and Organelles

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The lumen of the rough endoplasmic reticulum is continuous with _____ space.

TAP TO REVEAL ANSWER

The lumen of the rough endoplasmic reticulum is continuous with _____ space.

perinuclear

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