🧫 A&P I · Cell Biology

Memory tricks for the cell — the basic unit of life

Cell structure, organelles, membrane transport, the cell cycle, mitosis, and meiosis — cell biology is the foundation of all physiology. Understand the cell and you understand how every organ system works at its most fundamental level.

🧫 Cell Biology

Memory Tricks

Proven Mnemonics & Acronyms — fast to learn, hard to forget.

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Cell Theory
Three tenets — All cells from cells · Cells are basic units · All living things are cells
Cell theory: the foundational framework of all biology
The three principles of cell theory — and why they matter for A&P
All living organisms are composed of one or more cells. The cell is the basic structural and functional unit of life. All cells arise from pre-existing cells (cell division — no spontaneous generation). Human body contains ~37 trillion cells. Two major cell types: prokaryotic (no nucleus — bacteria) and eukaryotic (membrane-bound nucleus — all human cells). Human cells are eukaryotic. Cell size range: 2–200 micrometers. Red blood cells (7.5 μm) and muscle cells (up to 30 cm) illustrate the range. Cell shape reflects function — RBCs are biconcave for surface area, neurons have long axons for communication.
Prokaryotic
No membrane-bound nucleus. Bacteria and archaea. No membrane organelles.
Eukaryotic
Membrane-bound nucleus. All human cells, plants, fungi, protists.
37 trillion
Estimated cell count in human body. More bacteria than human cells on/in us.
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🃏 Cell Theory
Cell theory — the three tenets?
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🃏 Answer
Three tenets — All cells from cells · Cells are basic units · All living things are cells
ProkaryoticNo membrane-bound nucleus. Bacteria and archaea. No membrane organelles.
EukaryoticMembrane-bound nucleus. All human cells, plants, fungi, protists.
37 trillionEstimated cell count in human body. More bacteria than human cells on/in us.
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Cell Membrane Structure
Fluid Mosaic Model — phospholipid bilayer with floating proteins
Hydrophilic heads face out · Hydrophobic tails face in · Proteins float throughout
The plasma membrane — structure and the fluid mosaic model
The plasma membrane is a phospholipid bilayer — two layers of phospholipids arranged tail-to-tail. Each phospholipid has a hydrophilic (water-loving) head facing outward toward water, and two hydrophobic (water-fearing) fatty acid tails facing inward away from water. Fluid mosaic model: the membrane is fluid (phospholipids move laterally) and mosaic (proteins embedded throughout). Membrane proteins: integral proteins span the membrane (transport, receptors), peripheral proteins attach to surface (cytoskeleton anchor). Cholesterol embedded between phospholipids — stabilizes membrane, prevents it from being too rigid or too fluid. Glycoproteins and glycolipids on outer surface — cell recognition and identification (ABO blood type).
Phospholipid
Glycerol + phosphate head (hydrophilic) + 2 fatty acid tails (hydrophobic).
Cholesterol
Between phospholipids — stabilizes fluidity. More cholesterol = less fluid.
Integral proteins
Span membrane — channels, carriers, receptors, pumps.
Glycoproteins
Sugar chains on outer surface — cell ID, ABO blood type, immune recognition.
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🃏 Cell Membrane Structure
Plasma membrane — what is the fluid mosaic model?
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🃏 Answer
Fluid Mosaic Model — phospholipid bilayer with floating proteins
PhospholipidGlycerol + phosphate head (hydrophilic) + 2 fatty acid tails (hydrophobic).
CholesterolBetween phospholipids — stabilizes fluidity. More cholesterol = less fluid.
Integral proteinsSpan membrane — channels, carriers, receptors, pumps.
GlycoproteinsSugar chains on outer surface — cell ID, ABO blood type, immune recognition.
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Key Organelles
MERGE — Mitochondria · ER · Ribosome · Golgi · lysosomal Enzymes
Five organelles every A&P student must know cold
The five most important organelles — structure and function
Mitochondria: ATP production via oxidative phosphorylation. Double membrane. Own DNA — evidence of endosymbiosis. More mitochondria in high-energy cells (cardiac muscle). Endoplasmic reticulum: Rough ER (ribosomes attached → protein synthesis for export), Smooth ER (lipid synthesis, detox, Ca2+ storage in muscle). Ribosomes: protein synthesis — free ribosomes make cytoplasmic proteins, bound ribosomes make secretory proteins. Golgi apparatus: protein processing, sorting, packaging — "post office of the cell." Lysosomes: contain digestive enzymes at pH 4.5 — break down waste, cellular debris, and pathogens.
Mitochondria
ATP factory. Double membrane. Own DNA. Most in cardiac and skeletal muscle cells.
Rough ER
Ribosomes on surface — makes proteins for secretion or membrane insertion.
Smooth ER
Lipid synthesis, drug detox (liver), Ca2+ storage (muscle SR).
Golgi
Cis face receives (from ER), trans face ships. Glycosylation, sorting, vesicles.
Lysosomes
pH 4.5 acid environment. Hydrolytic enzymes. Failure → lysosomal storage disease (Tay-Sachs).
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🃏 Key Organelles
MERGE
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🃏 Answer
MERGE — Mitochondria · ER · Ribosome · Golgi · lysosomal Enzymes
MitochondriaATP factory. Double membrane. Own DNA. Most in cardiac and skeletal muscle cells.
Rough ERRibosomes on surface — makes proteins for secretion or membrane insertion.
Smooth ERLipid synthesis, drug detox (liver), Ca2+ storage (muscle SR).
GolgiCis face receives (from ER), trans face ships. Glycosylation, sorting, vesicles.
LysosomespH 4.5 acid environment. Hydrolytic enzymes. Failure → lysosomal storage disease (Tay-Sachs).
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Nucleus Structure
NEEN — Nuclear envelope · Endoplasmic reticulum connection · Enclosed DNA · Nucleolus
The control center of the cell — houses DNA and controls protein synthesis
The nucleus — four structural features and why each matters
The nucleus is the control center of the cell — contains the genetic instructions for making every protein. Nuclear envelope: double membrane punctuated by nuclear pores — controls what enters and exits (mRNA exits, transcription factors enter). Connected to rough ER — continuous membrane system. DNA: organized into chromosomes (46 in human somatic cells, 23 pairs). Chromatin = DNA + histone proteins. Condensed = chromosomes (visible during division). Dispersed = chromatin (during gene expression). Nucleolus: dense region within nucleus — site of ribosomal RNA (rRNA) synthesis and ribosome assembly. Cells with high protein output have large nucleoli.
Nuclear pores
Selective channels — mRNA exits, proteins (transcription factors, histones) enter.
46 chromosomes
23 pairs in somatic cells. 23 (haploid) in gametes. 22 pairs autosomes + 1 pair sex chromosomes.
Nucleolus
Makes rRNA → ribosome assembly. Disappears during cell division.
Histones
Proteins that DNA wraps around (nucleosome). Regulate gene access.
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🃏 Nucleus Structure
NEEN
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NEEN — Nuclear envelope · Endoplasmic reticulum connection · Enclosed DNA · Nucleolus
Nuclear poresSelective channels — mRNA exits, proteins (transcription factors, histones) enter.
46 chromosomes23 pairs in somatic cells. 23 (haploid) in gametes. 22 pairs autosomes + 1 pair sex chromosomes.
NucleolusMakes rRNA → ribosome assembly. Disappears during cell division.
HistonesProteins that DNA wraps around (nucleosome). Regulate gene access.
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Membrane Transport
PACE — Passive · Active · Co-transport · Endocytosis/Exocytosis
No energy vs energy required — direction of concentration gradient determines type
How substances cross the cell membrane — four transport categories
Passive transport: moves DOWN concentration gradient — no ATP. Simple diffusion (O2, CO2, lipids), facilitated diffusion (glucose via GLUT transporters, ions via channels), osmosis (water via aquaporins). Active transport: moves AGAINST gradient — requires ATP. Na+/K+ ATPase: 3 Na+ out, 2 K+ in per ATP — essential for nerve and muscle function. Secondary active transport (cotransport): uses Na+ gradient created by Na+/K+ pump to drive glucose/amino acid uptake. Endocytosis: phagocytosis (large particles), pinocytosis (fluid), receptor-mediated (specific molecules — LDL cholesterol). Exocytosis: secretion of proteins, hormones, neurotransmitters.
Simple diffusion
O2, CO2, lipid-soluble molecules — no protein needed, high to low concentration.
Facilitated
Glucose (GLUT), ions (channels) — protein assists, still down gradient.
Na+/K+ pump
3 Na+ out / 2 K+ in per ATP. Resting membrane potential. ~30% of resting ATP.
Osmosis
Water moves toward higher solute concentration. Aquaporins speed it up.
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🃏 Membrane Transport
PACE
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🃏 Answer
PACE — Passive · Active · Co-transport · Endocytosis/Exocytosis
Simple diffusionO2, CO2, lipid-soluble molecules — no protein needed, high to low concentration.
FacilitatedGlucose (GLUT), ions (channels) — protein assists, still down gradient.
Na+/K+ pump3 Na+ out / 2 K+ in per ATP. Resting membrane potential. ~30% of resting ATP.
OsmosisWater moves toward higher solute concentration. Aquaporins speed it up.
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Cell Cycle
IPMAT — Interphase · Prophase · Metaphase · Anaphase · Telophase
Interphase (G1, S, G2) · then Mitosis (PMAT) · then Cytokinesis
The cell cycle — what happens in each phase before and during division
Interphase (90% of cell cycle): G1 — cell grows, makes proteins, prepares for DNA replication. S phase — DNA synthesis (replication), chromosomes duplicated. G2 — final growth, organelle duplication, prepares for division. Mitosis (PMAT): Prophase — chromatin condenses into visible chromosomes, spindle forms. Metaphase — chromosomes align at middle (metaphase plate). Anaphase — sister chromatids pulled to opposite poles. Telophase — nuclear envelopes reform, chromosomes decondense. Cytokinesis: cytoplasm divides → 2 identical daughter cells. Checkpoints: G1, G2, and M checkpoints ensure DNA is undamaged before proceeding. Cancer = checkpoint failure.
G1 phase
Growth and protein synthesis. Most variable phase. G1 checkpoint: DNA damage check.
S phase
DNA replication — each chromosome duplicated → sister chromatids held at centromere.
Mitosis
PMAT — 46 chromosomes → two cells each with 46. Somatic cell division.
Cancer
Checkpoint genes (p53, Rb) mutated → uncontrolled division → tumor.
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🃏 Cell Cycle
IPMAT
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🃏 Answer
IPMAT — Interphase · Prophase · Metaphase · Anaphase · Telophase
G1 phaseGrowth and protein synthesis. Most variable phase. G1 checkpoint: DNA damage check.
S phaseDNA replication — each chromosome duplicated → sister chromatids held at centromere.
MitosisPMAT — 46 chromosomes → two cells each with 46. Somatic cell division.
CancerCheckpoint genes (p53, Rb) mutated → uncontrolled division → tumor.
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Mitosis vs Meiosis
Mitosis = More identical · Meiosis = Mix and halve
Mitosis: 1 cell → 2 identical diploid · Meiosis: 1 cell → 4 unique haploid gametes
Mitosis vs meiosis — why the body needs both
Mitosis: for growth and repair. One diploid cell (46 chromosomes) → two genetically identical diploid daughter cells (46 chromosomes each). One round of division. No crossing over. Meiosis: for sexual reproduction. One diploid cell → four genetically unique haploid cells (23 chromosomes each — sperm or eggs). Two rounds of division (Meiosis I and II). Crossing over in Prophase I creates genetic recombination — shuffles genes. Fertilization restores diploid number (23 + 23 = 46). Nondisjunction: failure of chromosomes to separate → aneuploidy. Trisomy 21 (Down syndrome) = extra chromosome 21.
Mitosis
2n → 2n. One division. Identical cells. Growth, repair, replacement.
Meiosis I
Homologous pairs separate. Crossing over. 2n → 2n (but recombined).
Meiosis II
Sister chromatids separate (like mitosis). 2n → n. 4 haploid cells total.
Nondisjunction
Chromosomes fail to separate → extra or missing chromosome. Down syndrome, Turner, Klinefelter.
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🃏 Mitosis vs Meiosis
Mitosis vs meiosis — how do they differ?
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🃏 Answer
Mitosis = More identical · Meiosis = Mix and halve
Mitosis2n → 2n. One division. Identical cells. Growth, repair, replacement.
Meiosis IHomologous pairs separate. Crossing over. 2n → 2n (but recombined).
Meiosis IISister chromatids separate (like mitosis). 2n → n. 4 haploid cells total.
NondisjunctionChromosomes fail to separate → extra or missing chromosome. Down syndrome, Turner, Klinefelter.
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Cytoskeleton
MIM — Microfilaments · Intermediate filaments · Microtubules
Three cytoskeletal fibers — thin to thick, different functions
The cytoskeleton — cell shape, movement, and internal transport
The cytoskeleton is the cell's internal scaffolding — it maintains shape, enables movement, anchors organelles, and provides tracks for intracellular transport. Microfilaments (thinnest, 7 nm): actin filaments — muscle contraction, cell movement, cell division (contractile ring). Intermediate filaments (10 nm): keratin, vimentin, desmin — structural support, resist mechanical stress, anchor nucleus. Microtubules (thickest, 25 nm): tubulin — cell shape, mitotic spindle (chromosome movement), cilia and flagella (9+2 arrangement), motor protein tracks (kinesin and dynein move organelles). Centrioles: two perpendicular microtubule cylinders — form spindle during cell division.
Microfilaments
Actin (7 nm). Muscle contraction, pseudopod formation, cytokinesis contractile ring.
Intermediate
Keratin, vimentin (10 nm). Mechanical strength, nuclear anchoring.
Microtubules
Tubulin (25 nm). Spindle, cilia, flagella, organelle transport tracks.
Cilia vs flagella
Cilia: short, many (respiratory tract — sweeps mucus). Flagella: long, one (sperm tail).
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🃏 Cytoskeleton
MIM
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🃏 Answer
MIM — Microfilaments · Intermediate filaments · Microtubules
MicrofilamentsActin (7 nm). Muscle contraction, pseudopod formation, cytokinesis contractile ring.
IntermediateKeratin, vimentin (10 nm). Mechanical strength, nuclear anchoring.
MicrotubulesTubulin (25 nm). Spindle, cilia, flagella, organelle transport tracks.
Cilia vs flagellaCilia: short, many (respiratory tract — sweeps mucus). Flagella: long, one (sperm tail).
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Protein Synthesis
DNA → Transcription → mRNA → Translation → Protein
Central dogma — information flows from DNA to RNA to protein
How cells make proteins — transcription in nucleus, translation at ribosome
Transcription (nucleus): DNA unwinds → RNA polymerase reads template strand → builds complementary mRNA strand (A-U, T-A, G-C, C-G). mRNA processed (introns removed, exons spliced together, 5' cap and poly-A tail added) → exits nucleus through nuclear pores. Translation (ribosome): ribosome reads mRNA codons (3 bases = 1 amino acid) → tRNA brings matching amino acid (anticodon matches codon) → peptide bonds form amino acid chain → polypeptide released. 64 codons, 20 amino acids, 3 stop codons (UAA, UAG, UGA). Mutations: substitution, insertion, deletion — can alter protein function.
Transcription
DNA → mRNA. In nucleus. RNA polymerase. Template strand read 3' to 5', mRNA built 5' to 3'.
mRNA processing
Introns (intervening) removed, exons (expressed) kept. 5' cap + poly-A tail added.
Translation
mRNA → protein. At ribosome. tRNA anticodon matches mRNA codon → amino acid added.
Codon
3-base code on mRNA. 64 total — 61 code for amino acids, 3 are stop codons.
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🃏 Protein Synthesis
Protein synthesis — the steps, and where each happens?
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🃏 Answer
DNA → Transcription → mRNA → Translation → Protein
TranscriptionDNA → mRNA. In nucleus. RNA polymerase. Template strand read 3' to 5', mRNA built 5' to 3'.
mRNA processingIntrons (intervening) removed, exons (expressed) kept. 5' cap + poly-A tail added.
TranslationmRNA → protein. At ribosome. tRNA anticodon matches mRNA codon → amino acid added.
Codon3-base code on mRNA. 64 total — 61 code for amino acids, 3 are stop codons.
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