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Here is a structured summary of Cytology Lecture 6 – Cell Signaling, Tissue Organization & Cell Turnover (34 slides, Geomedi 2026, Dr. Giorgi Berishvili):

Part I: Cell Signaling

Why cells signal Cells must communicate to survive, grow, and function - both as single-celled organisms and as part of multicellular tissues. Signaling involves three steps: transmission (signal molecule released), reception (receptor on target cell binds it), and interpretation (intracellular response alters cell behavior).
Types of signaling
TypeMechanism
EndocrineHormones travel via bloodstream (systemic)
Paracrine/AutocrineLocal mediators act on nearby/same cells
NeurotransmissionNeurotransmitters at synapses
Direct contactCell surface signaling molecules
Receptors
  • Cell surface receptors - for signals that cannot cross the membrane
  • Intracellular receptors - for lipophilic molecules (e.g., steroids) that enter the cell; act as transcription factors in the nucleus
Three classes of cell surface receptors
  1. Ion channel-coupled - change membrane permeability to ions
  2. G-protein-coupled receptors (GPCRs) - activate trimeric G proteins
  3. Enzyme-coupled receptors - act as or associate with enzymes
Intracellular signaling pathways Signal cascades relay, amplify, or suppress signals through positive/negative feedback loops. Multiple pathways interact to produce combined responses.

Part II: Tissue Organization

Basic tissues Cells organize into 4 basic tissue types: Nervous, Muscular, Epithelial, and Connective. Cells are held together by cell-cell adhesions and the extracellular matrix (ECM).
Extracellular Matrix (ECM)
  • A network of proteins and polysaccharides filling the space between cells
  • Functions: structural support, cell adhesion (via integrins), cell migration, growth factor binding, barrier function, wound healing
  • Abnormal ECM remodeling can lead to fibrosis or cancer metastasis
Key ECM components
  • Collagen - triple helix synthesized by fibroblasts; provides tensile strength; cells attach via integrin-fibronectin linkage
  • Proteoglycans - protein core + glycosaminoglycans (GAGs) like hyaluronan; attract water, form a hydrated gel, resist compression; bones are hardened by calcium phosphate impregnation
  • Basal lamina (basement membrane) - 50-200 nm sheet of type IV collagen + laminin; underlies epithelia, surrounds nerves and muscle; thickening of glomerular basement membrane can cause kidney failure
Cell junctions Tissue-specific junctions vary in strength:
TissueDominant Junctions
EpithelialTight, adherens, desmosomes, gap junctions
MuscleDesmosomes, gap junctions, adherens
NervousSynapses, gap junctions, CAMs
ConnectiveECM-integrin interactions
ImmuneSelectins, integrins (variable/transient)

Part III: Cell Turnover

Cell turnover overview Continuous process of cell renewal and replacement through proliferation, differentiation, and death to maintain tissue homeostasis.
Cell death: Necrosis vs. Apoptosis
NecrosisApoptosis
CauseInjuryProgrammed (PCD)
ProcessSwelling and burstingCondensation and shrinkage
Effect on neighborsHarmful (releases contents)Safe (phagocytes engulf fragments)
Content fateLostRecycled
~5 × 10¹¹ blood cells are cleared by apoptosis daily in humans; ~half of neurons are eliminated by PCD during development.
Apoptosis mechanism - Caspases
  • Driven by a cascade of proteolytic reactions involving caspases (cysteine-containing aspartate proteases)
  • Caspases cleave hundreds of target proteins, activating some and inactivating others
Intrinsic (mitochondrial) pathway DNA damage or oxidative stress → cytochrome c release from mitochondria → apoptosome formation → procaspases activated → protein cleavage + DNA fragmentation
Bcl-2 family regulates intrinsic pathway - balance between pro- and anti-apoptotic members determines cell fate.
Extrinsic pathway Fas receptor on cell surface activated by Fas ligand on immune cells; also induced by TGF-β and TNF; can amplify through the intrinsic pathway.
Survival signals
  • Survival factors - suppress apoptosis
  • Mitogens - stimulate cell division (proliferation)
  • Growth factors - stimulate cell growth (increase in mass)
  • Survival is NOT the default state - it must be continuously signaled.
Tissue renewal rates
TissueRenewal Time
Gut epithelium3-6 days
Epidermis~2 months
Red blood cells120 days
Bone~10 years
NeuronsLifetime (most)
Stem cells
  • Terminally differentiated cells are replenished by progenitor cells, which arise from stem cells via asymmetric division (one SC + one progenitor)
  • Intestinal epithelium - stem cells at crypt base → progenitors in crypt → differentiated cells on villi → shed into lumen
  • Hematopoietic SCs - multipotent; reside in bone marrow niche; at least 20 colony-stimulating factors/hematopoietic growth factors drive differentiation
  • Embryonic stem cells (ESCs) - pluripotent; can become any cell type with appropriate growth factor cocktails
  • Induced pluripotent stem cells (iPSCs) - adult mature cells reprogrammed to a pluripotent ES-like state by activating transcription regulators; key to regenerative medicine via cell-replacement therapy

Key exam points to remember:
  1. Three steps of cell signaling: transmission, reception, interpretation
  2. Three classes of cell surface receptors (ion channel, GPCR, enzyme-coupled)
  3. ECM components: collagen, proteoglycans, basal lamina
  4. Apoptosis vs. necrosis differences
  5. Intrinsic (mitochondrial) vs. extrinsic apoptotic pathways; role of Bcl-2
  6. Caspases as the executioners of apoptosis
  7. Stem cell hierarchy: SC → progenitor → differentiated cell
  8. iPSCs and their therapeutic potential

Give me MCQ type questions from this pdf

Here are 30 MCQ-style exam questions based on Cytology Lecture 6:

Part I: Cell Signaling

1. Which of the following correctly describes the sequence of cell signaling?
  • A) Reception → Transmission → Interpretation
  • B) Transmission → Interpretation → Reception
  • C) Transmission → Reception → Interpretation ✓
  • D) Interpretation → Reception → Transmission

2. A hormone is released from the pancreas and travels through the bloodstream to affect liver cells. This is an example of:
  • A) Paracrine signaling
  • B) Autocrine signaling
  • C) Neurotransmission
  • D) Endocrine signaling ✓

3. A cell releases a signal molecule that acts back on itself. This is called:
  • A) Endocrine signaling
  • B) Autocrine signaling ✓
  • C) Paracrine signaling
  • D) Direct contact signaling

4. Which type of receptor changes membrane permeability to ions upon activation?
  • A) G-protein-coupled receptor
  • B) Enzyme-coupled receptor
  • C) Ion channel-coupled receptor ✓
  • D) Intracellular receptor

5. A lipophilic signaling molecule crosses the plasma membrane and binds to a receptor that directly activates gene transcription. This receptor is best classified as:
  • A) GPCR
  • B) Ion channel-coupled receptor
  • C) Enzyme-coupled receptor
  • D) Nuclear (intracellular) receptor ✓

6. G-protein-coupled receptors activate which of the following?
  • A) Ion channels directly
  • B) Trimeric GTP-binding proteins (G proteins) ✓
  • C) Nuclear transcription factors
  • D) Caspases

7. Intracellular signaling pathways that relay and modulate extracellular signals often involve:
  • A) Direct membrane-to-membrane contact only
  • B) Only positive feedback mechanisms
  • C) Positive and negative feedback mechanisms ✓
  • D) Signal degradation without amplification

8. Which statement about intracellular signaling is TRUE?
  • A) Each signal follows a single, independent pathway
  • B) Pathways never interact with each other
  • C) Various pathways interact to amplify, suppress, or distribute signals ✓
  • D) Only extracellular signals can interact

Part II: Tissue Organization

9. Which are the four basic tissue types in multicellular organisms?
  • A) Epithelial, Connective, Vascular, Nervous
  • B) Nervous, Muscular, Epithelial, Connective ✓
  • C) Muscular, Lymphoid, Epithelial, Bone
  • D) Connective, Glandular, Nervous, Muscular

10. The extracellular matrix (ECM) anchors cells via which molecules?
  • A) Cadherins
  • B) Gap junctions
  • C) Integrins ✓
  • D) Tight junction proteins

11. Abnormal ECM remodeling is associated with which conditions?
  • A) Apoptosis and necrosis
  • B) Stem cell differentiation failure
  • C) Fibrosis and cancer metastasis ✓
  • D) Ion channel dysfunction

12. Collagen triple helix is synthesized by which cells?
  • A) Osteoclasts
  • B) Epithelial cells
  • C) Fibroblasts ✓
  • D) Macrophages

13. Proteoglycans resist compression because they:
  • A) Form covalent cross-links with collagen
  • B) Activate integrin signaling
  • C) Attract water and form a hydrated gel ✓
  • D) Harden bone by calcium phosphate deposition

14. The glycosaminoglycan (GAG) that is a key component of proteoglycans is:
  • A) Fibronectin
  • B) Laminin
  • C) Collagen type IV
  • D) Hyaluronan ✓

15. The basal lamina (basement membrane) is composed of:
  • A) Collagen type I and fibronectin
  • B) Elastin and laminin
  • C) Collagen type IV and laminin ✓
  • D) Proteoglycans and fibrillin

16. Abnormal thickening of basement membranes surrounding the glomeruli leads to:
  • A) Liver cirrhosis
  • B) Myocardial infarction
  • C) Kidney failure ✓
  • D) Neurodegeneration

17. Which tissue type has the lowest adhesion strength and relies mainly on ECM-integrin interactions?
  • A) Epithelial
  • B) Muscle
  • C) Nervous
  • D) Connective ✓

18. Which cell junctions are found in epithelial tissue but NOT listed as dominant in connective tissue?
  • A) Gap junctions
  • B) ECM-integrin interactions
  • C) Tight junctions and desmosomes ✓
  • D) Synapses

Part III: Cell Turnover

19. Which form of cell death is considered harmful to surrounding cells because it releases cellular contents?
  • A) Apoptosis
  • B) Autophagy
  • C) Necrosis ✓
  • D) Anoikis

20. Approximately how many blood cells are cleared daily in humans by apoptosis?
  • A) 5 × 10⁸
  • B) 5 × 10⁹
  • C) 5 × 10¹⁰
  • D) 5 × 10¹¹ ✓

21. The proteases that drive apoptosis by cleaving hundreds of target proteins are:
  • A) Matrix metalloproteinases
  • B) Serine proteases
  • C) Caspases ✓
  • D) Ubiquitin ligases

22. In the intrinsic apoptotic pathway, what is released from mitochondria to trigger caspase activation?
  • A) Bcl-2
  • B) TNF
  • C) Fas ligand
  • D) Cytochrome c ✓

23. The complex in which procaspases are activated during intrinsic apoptosis is called the:
  • A) Proteasome
  • B) Inflammasome
  • C) Apoptosome ✓
  • D) Spliceosome

24. Cell fate in the intrinsic apoptotic pathway is determined by the balance between pro- and anti-apoptotic members of which protein family?
  • A) Caspase family
  • B) Bcl-2 family ✓
  • C) TNF receptor family
  • D) Integrin family

25. Which of the following factors does NOT induce apoptosis via the extrinsic pathway?
  • A) Fas ligand
  • B) TGF-β
  • C) TNF
  • D) Cytochrome c ✓
(Cytochrome c is part of the intrinsic pathway)

26. Which of the following correctly describes survival signals?
  • A) Survival factors stimulate cell division; mitogens suppress apoptosis
  • B) Growth factors stimulate cell division; mitogens stimulate cell growth
  • C) Survival factors suppress apoptosis; mitogens stimulate cell division ✓
  • D) Growth factors eliminate damaged cells

27. Which tissue has the fastest renewal rate?
  • A) Epidermis (~2 months)
  • B) Red blood cells (120 days)
  • C) Gut epithelial cells (3-6 days) ✓
  • D) Bone (~10 years)

28. In intestinal epithelium, where are stem cells located?
  • A) On top of the villi
  • B) In the middle of the crypt
  • C) On the surface facing the gut lumen
  • D) At the bottom of the crypt ✓

29. Hematopoietic stem cells are described as multipotent because they:
  • A) Can give rise to any cell type in the body
  • B) Can only produce red blood cells
  • C) Can give rise to a large but limited range of differentiated blood cell types ✓
  • D) Divide symmetrically to produce identical daughter cells

30. Induced pluripotent stem cells (iPSCs) differ from embryonic stem cells (ESCs) in that:
  • A) iPSCs cannot differentiate in vitro
  • B) iPSCs are less useful for regenerative medicine
  • C) ESCs are derived from reprogrammed adult cells
  • D) iPSCs are derived from reprogrammed mature adult cells ✓

Quick scoring guide: 27-30 correct = Excellent | 22-26 = Good | 18-21 = Review needed | <18 = Revisit the lecture
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