chap 2- the cell & its functions (b1- foundation) Flashcards

1
Q

2 major parts of the cell

A

nucleus and cytoplasm

  • nucleus is separated from cytoplasm by nuclear membrane
  • cytoplasm is separated from the surrounding fluids by cell membrane (plasma membrane)
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2
Q

protoplasm + 5 basic substances

A

the different substances that make up the cell (“the living part of the cell”) - includes everything inside the cell membrane

5 basic substances: water, electrolytes, proteins, lipids, and carbohydrates

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3
Q

importance of cell membrane

A
  • Protective mechanical barrier
  • Allows cell recognition
  • Determine composition of cells
  • Maintain ion concentration difference between ICF and ECF.
  • Cell to cell communication

straight from slides

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4
Q

composition of the cell membrane (in percents)

A

protein: 55%
phospholipids: 25%
cholesterol: 13%
other lipids: 4%
carbohydrates: 3%

she said to know this

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5
Q

components of cell membrane: lipids (3 types)

A
  1. phospholipids: most abundant in cell membrane, hydrophilic polar head with hydrophobic non-polar tails
    - middle is permeable to fat soluble molecules (O2, CO2, alcohol) and impermeable to water soluble molecules (ions, glucose, urea)
  2. sphingolipids: complex sphingolipids protect from harmful environment factors, do signal transmission, and are adhesion sites for extracellular proteins
    - derived from amino alcohol sphingosine
    - present in small amounts
  3. cholesterol: help determine the degree of permeability and control fluidity
    - are dissolved in the lipid bilayer
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6
Q

components of cell membrane: proteins (2 types- another flashcard does them in detail)

A

integral and peripheral

  • membrane proteins are mainly glycoproteins
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7
Q

glycocalyx + 4 main functions (imp)

A

“glyco-“ portions (glycolipids & glycoproteins) protrude towards outside of cell

proteoglycans: loosely attached to outer surface of cell

together form the glycocalyx which is the “sugar coating” on the outside of cell membrane which has functions:

  1. Have negative electrical charge that give cells overall negative charge to repel other negatively charged objects
  2. glycocalyx of some cells attaches to glycocalyx of other cells for cell to cell interaction
  3. act as receptors for binding hormones (such as insulin)
  4. role in immune reactions & self-identity marker
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8
Q

lipid rafts

A

small, specialized areas in cell membrane that are needed for communication between cells

  • have proteins in them that act as receptors to extracellular chemical messengers

are rich in cholesterol & sphingolipids

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9
Q

integral proteins + 4 types & their functions

A

protrude all the way through the membrane

1. Channels: water-filled pores: allow specific molecules only (usually water or ions) to diffuse through
- ex. aquaporins

2. Carrier Proteins: bind to a specific molecule inducing a conformational change that then transports the molecule across the membrane
- can also do active transport to go against the electrochemical gradient
- ex. glucose transporter (GLUT)

3. Enzymes: speed up chemical reactions on the membrane
- ex. ATP Synthase in mitochondria

4. Receptors (for water-soluble chemicals): specific ligands bind to receptor causing conformational change in receptor protein
- triggers response inside cell using second messengers to relay the signal inside

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10
Q

peripheral proteins + 6 types & their functions

A

attached only to the surface of the membrane and do not penetrate all the way through
- usually attached to integral proteins

1. Membrane Bound Enzymes: enzymes attaches to the membrane that help speed up chemical reactions
- ex. acetylcholinesterase

2. Controllers of transport through pores: regulate channel or pore activity by opening/closing when needed
- ex. regulatory proteins that control ion channels in nerve cells

3. Cell Adhesion Molecules (CAMs): protrude from membrane surface that help cells stick to each other or to surfaces (imp for tissue formation)
- ex. interns that help cells attach to surroundings

4. Cell identity markers (w/ carbs): proteins combine with carbs (glycoproteins) that act like ID card for cell
- ex. MHC

5. Docking marker acceptor: on inner surface for secretory vesicles, help vesicles dock and release their contents (exocytosis)
- ex. SNARE proteins guide vesicles carrying neurotransmitters to the membrane

6. Enzymes: not bound to membrane but help out in reactions nearby
- ex. adenylate cyclase, which helps make cAMP, important signaling molecule

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11
Q

fluid mosaic model + parts

A

structure of cell membrane is not solid but rather “fluid” that is flexible and moves freely

also a mosaic bc a mixture of different parts that include:
- phospholipid bilayer
- proteins (integral & peripheral)
- cholesterol
- carbohydrates

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12
Q

membranous vs non-membraneous organelles

A

membranous:
- Endoplasmic reticulum
- Golgi complex
- Lysosomes
- Peroxisomes
- Mitochondria

non-membranous:
- Ribosomes
- Proteasomes
- Vaults
- Centrioles
- Cytoskeleton

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13
Q

what type of cells might have more than 1 nuclei or no nuclei?

A

example was of skeletal muscle cells & RBC’s have no nuclei

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14
Q

structure of the nuclear membrane (aka nuclear envelope)

A

2 separate bilayer membranes with the outer membrane continuous with the Endoplasmic reticulum membrane and has ribosomes attached to it

  • penetrated by several nuclear pores that allow molecules through
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15
Q

nucleolus

A
  • darkly stains
  • has no limiting membrane but instead is just a dense collection of RNA & proteins
  • enlarges when cell is synthesizing
  • place for synthesis of ribosomes
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16
Q

chromatin

A
  • fibers of DNA & proteins
  • stores information for synthesis of proteins
  • contains genetic info
  • arrangement into chromosomes
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17
Q

structure of nucleus

A

nuclear envelope: protective shell around the nucleus (made of 2 layers- inner and outer membrane), keeps DNA safe inside while separating it from the rest of the cell

nuclear pores (nucleoporins): tiny holes in the nuclear envelope, act like gates allowing important molecules (RNA and proteins) to move in and out of cell while keeping harmful substances out

nuclear lamina (jali like region): line inner part of the nuclear envelope, providing support and helps maintain shape of the nucleus

nucleolus: dense, round structure inside the nucleus, site where ribosomes are made

nucleoplasm: gel-like substance inside nucleus that surrounds the DNA and nucleolus (contains enzymes, proteins, and other molecules needed for the nucleus to function)

think nuclear EPL

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18
Q

functions of the nucleus

A
  • controls hereditary characteristics of an organism & stores hereditary material in the form of DNA
  • responsible for cell division, growth, and differentiation
  • produces ribosomes (protein factories)
  • site for transcription (mRNA are produced for protein synthesis*
  • involved in DNA repair
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19
Q

structure of mitochondria

A

2 lipid bilayer membrane - outer and inner membrane

  • inner membrane contains inholdings called cristae that increase surface area, and have oxidative enzymes attached to it for electron transport chain
  • inside is filled with matrix that contains enzymes for Krebs cycle (citric acid cycle) \
  • the outer layer is smooth
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20
Q

mitochondrial reticulum

A

network of interconnected mitochondria inside cell
- instead of separate, round mitochondria, are joined together in a web-like structure

benefits:
- helps cell distribute energy (ATP) more efficiently
- allows mitochondria to share resources like proteins and DNA
- helps in cell signaling and responding to stress

  • common in muscle (skeletal) cells, where energy needs to be spread quickly and evenly
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21
Q

what does it mean by “mitochondria network is dynamic”?

A

expands in response to contractile activity (exercise) in skeletal muscle

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22
Q

what is the role of mitochondria in programmed cell death? (imp)

A

mitochondria receives signal to self-destruct (apoptosis) → releases cytochrome c (protein normally used in energy production) into the cytoplasm → activates intra-cellular protein snipping enzymes → slice cell into small, disposable pieces

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23
Q

what are functions of the mitochondria?

A
  • ATP production
  • Role in apoptosis
  • Storage of Ca2+
  • heat production (in brown fat cells through thermogenesis)
  • ketone bodies production (in the matrix)
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24
Q

3 unique features of the mitochondria

A
  • self replicating (also has it’s own DNA thats more prone to mutations)
  • maternal inheritance
  • number per cells vary according to energy cells
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25
functions of the rough endoplasmic reticulum
- transport of substances - protein formation (sort and processing) - sends proteins to their destinations
26
what type of cells is rough ER extensive in?
extensive in cells specialized for **protein secretion** (cells that secrete digestive enzymes) and cells that require extensive **membrane synthesis** (growing cells such as immature egg cells).
27
structure of endoplasmic reticulum
network of tubular & flat vesicular structures present in the cytoplasm - walls made of **lipid bilayer** - space inside tubules and vesicles is filled with **endoplasmic matrix**
28
function of ribosomes
composed of a mixture of **rRNA + ribosomal proteins** Function: - translates mRNA into chains of amino acids - Brings togethers mRNA, tRNA, and amino acids - Provides enzymes and energy for protein formation
29
functions of the smooth endoplasmic reticulum
- **Lipid synthesis** (esp phospholipids and cholestrol that are rapidly integrated into the lipid bilayer growing the endoplasmic reticulum) - Provide **enzymes** for glycogen breakdown - **Detoxification** of substances e.g drugs (in liver by coagulation, oxidation, hydrolysis etc) - Stores and releases **calcium ions** (in muscles as sarcoplasmic reticulum)
30
ER exit site & COPII (coat protein II)
**ER exit site**: where newly made proteins and lipids leave the smooth endoplasmic reticulum to be sent to the Golgi apparatus for further processing - happens through vesicle formation that is controlled by protein coat **COPII** **COPII**: these proteins recognize & attach to specific proteins on the **smooth ER membrane** at the exit site - COPII proteins then start to **curve the ER membrane** forming a dome-shaped bud around newly synthesized products → vesicles then branch off to move towards the Golgi apparatus (the lipids that are synthesized are constantly going into the lipid membrane so to prevent overgrowth, these vesicles pop off the smooth ER)
31
ubiquitin-proteasome pathway
used by cells to **identify & destroy misfolded, damaged, or unneeded proteins** misfolded proteins → tagged with **ubiquitin (doom tag)** → labelled flawed protein for destruction → directed out of ER to one of the many proteasomes to be SLICED
32
proteasome (nonmembranous organelle) function
protein degradation machine **function**: multiple protein-digesting enzymes break down ubiquinated proteins into recyclable building blocks
33
structure of Golgi complex
- Membranes similar to SER. - Composed of four or more **stacked layers** of parallel, thin, flat enclosed vesicles or **cisternae** - Prominent in secretory cells.
34
functions of the endoplasmic reticulum
- Processing of products formed in endoplasmic reticulum: a: **processing** of the raw material into finished products. b: **Sorting and directing** the finished product to their **final destination** - Synthesis of **certain carbohydrates** (like *hyaluronic acid and chondroitin sulfate*) - Sorts and packages products into secretory vesicles
35
I cell disease (Golgi apparatus)
happens when failure of Golgi apparatus to add phosphate tag to **mannose** - M6P protein is missing and ends up secreted outside of the cell instead of going to the lysosome - inherited disorder - **features**: coarse facial features, clouded cornea, restricted joint movements, high plasma levels of lysosomal enzymes - fatal in child hood
36
exocytosis is stimulated by entry of what ions?
**calcium ions** - calcium ions interact with the vesicular membrane and cause its fusion w/ the cell membrane, followed by *exocytosis*-- opening of the membrane's outer surface and extrusion of content inside cell
37
proteoglycans vs glycoproteins
**glycoproteins** → more proteins, less carbs **proteoglycans** → subclass of glycoproteins, but have more glucose (carbohydrate) than proteins
38
steps for packaging, docking, and release of secretory vesicles (using vSNARE docking markers)
Recognition markers in membrane of outermost golgi sac capture and bind with sorting signals of protein to be secreted → membrane closes beneath the bud, pinching off the secretory vesicle → vesicle loses its coating, exposing **v-SNARE docking markers** on the vesicle surface → v-SNAREs bind *ONLY* with the **t-SNARE docking marker acceptors** of the targeted plasma membrane, ensuring that secretory vesicles empty the contents to the cell’s exterior
39
4 types of hydrolases in lysosomes
**polysaccharide hydrolyzing enzymes**: digest polysaccharides into simpler sugars - ex. *beta-galactosidase, alpha-glucosidase, lysozyme* **lipid hydrolyzing enzymes**: digest lipids (fats & phospholipids) - ex. *fatty acyl esterase, phospholipases* **protein hydrolyzing enzymes**: digest proteins into smaller peptides or amino acids - ex. *cathepsins, collagenase, elastase, peptidases* **nucleic acid hydrolyzing enzymes**: digest genetic material (DNA & RNA) - ex. *ribonuclease, deoxyribonuclease*
40
2 ways that peroxisomes are different from lysosomes
1. formed by self-replication (or by budding off from smooth ER) instead of from Golgi apparatus (like lysosomes) 2. contain **oxidases** rather than hydrolases
41
secretory lysosomes + 3 examples
**secretory lysosomes**: unlike regular lysosomes (that break down waste), they store and release bioactive molecules in response to specific signals 1. **perforin**: protein that immune cells use to kill virus-infected cells - present in *cytotoxic T lymphocytes & natural killer cells* 2. **melanin**: pigment protein for hair, skin, and eye color - present in *melanocytes* 3. **serotonin**: neurotransmitter and signaling molecule that affects mood, blood clotting, and inflammation - present in *mast cells*
42
4 functions of lysosomes
**1. Cellular digestion**: digest waste, foreign invaders, and damaged cell parts - *residual body: leftover waste after digestion by lysosome* **2. Role In immunity**: - **lysozyme**: dissolves bacterial cell walls, tearing them apart - **lysoferrin**: binds iron, preventing bacteria from using it to grow - **acidic pH**: (~5.0) - acidic environment helps activate lysosomal enzymes to digest pathogens effectively **3. Regression of tissues**: help break down excess cells - *ex. of uterus shrinking after pregnancy* **4. Autophagy (self-eating)**: remove digested or damaged organelles to keep cells healthy
43
3 examples of lysosomal storage diseases
- tay sachs - gaucher disease - fabry disease
44
enzymes in peroxisomes
Peroxisomes contain over 40 enzymes, mainly: **Catalases** → Break down hydrogen peroxide (H₂O₂) into water and oxygen, preventing cell damage. **Oxidases** → Use oxygen (O₂) to remove hydrogen (H⁺) from organic molecules, producing H₂O₂ as a byproduct.
45
PPARs (peroxisome proliferator-activated receptors) and peroxins
**PPARs**: nuclear regulators that regulate formation of new peroxisomes by increasing numbers when needed - respond to fatty acids & other signals to enhance lipid metabolism **peroxins**: chaperone proteins that help transport proteins into peroxisomes so they can function properly
46
functions of peroxisomes
1. **β-oxidation of long chain fatty acids**: fatty acids are broken down into smaller molecules 2. **Detoxification of harmful chemicals**: remove toxins via oxidases (use O2 to neutralize harmful substances) - leads to production of **hydrogen peroxide (H2O2)** 3. **Removal of H2O2**: catalase quickly converts the H2O2 to water (H2O) and oxygen (O2) to prevent cell damage 4. **synthesis of important molecules**: like Bile acids, myelin and cholesterol 5. **Breakdown of purines into uric acid**: if uric acid builds up, can lead to gout which is a painful joint condition
47
microtubules are mainly composed of which protein?
tubulin
48
structure of **microtubule**
made of protein **tubulin**, specifically α-tubulin and β-tubulin, which form dimers that stack together (like a long dandi thats kind of hollow in the middle) - long, hollow, unbranched tubes are also the **largest** components of the cytoskeleton
49
functions of microtubules
**1. Positioning organelles**: help position cytoplasmic organelles within the cell (*lil baby organizers*) **2. Maintain cell shape/structure**: esp for cells that are asymmetric like neurons that need support **3. Facilitate complex movements**: act as tracks for intracellular transport - help move *vesicles*, organelles, and molecules **4. Stabilize neuron axons**: along with intermediate filaments, support long axons in neurons, preventing them from collapsing **5. Cilia & Flagella**: microtubules are the main structural components of cilia and flagella and help them move **6. Form mitotic spindle**: during mitosis and meiosis, help separate chromosomes and distribute them into daughter cells *basically stability for structure and conveyer belts*
50
3 components of the cytoskeleton
- microtubules (largest) - intermediate filaments - microfilaments (smallest)
51
axonal transport
in neurons, chemicals formed in cell body need to be transported to the axon to reach the synapse happens along microtubules that act as the **highways** for transporting vesicles, organelles, and proteins along the axon **motor proteins** (like kinesis & dynein) attach to these particles & use ATP to "walk" along the microtubules while carrying their cargo to destination *basically the moving across the highway is axonal transport*
52
kinesin (globular *motor protein*)
has two "feet," a stalk, and a fan like tail and **carries secretory vesicles** to the end of an axon - uses tubulin molecule (microtubules) as stepping stones - expenditure of ATP *lil cutie carrying that cargo on the highway and steps so funny too awww*
53
dynein vs kinesin
kinesin is the motor protein that moves "forward" (toward the cell membrane) while dynein moves "backward" (back to the nucleus or cell center) **dyenin**: carries debris vesicles back (which have waste and stuff) but also uses ATP like kinesin
54
myosin V
**myosin V**: motor protein that carries things inside the cell (*like delivery truck*) - walks along **actin filaments** (different from axonal transport where they walk across microtubules and that is long distance) - does **short-distance transport** *different from myosin II which is responsible for muscle contractions and works by forming thick filaments*
55
reverse axonal transport + effects
dynein moves in the opposite direction (instead of going back to cell center, goes to the cell membrane) inside of nerve cells some viruses can hijack dynein to cause this including: - **poliomyelitis virus** - **rabies virus** - **herpes virus**
56
do dynein and kinesin only exist in nerve cells?
no, but they play role in neurons bc neurons are long and need long distance transport **dynein**: found in all cells that use microtubules for transport, also in cilia and flagella (to help with movement) **kinesin**: important in cell division, ensuring chromosomes separate correctly
57
structure of cilia & flagella (axoneme, basal body)
basic internal structure is the same for both **axoneme**: total internal structure, made of microtubules and arranged in **9+2** structure (9 pairs of microtubules [doublets] arranged in a circle, 2 single microtubules in the center, outer doublets connected to each other by *dynein*) **centriole** move into the cell membrane, forming the basal body **basal body**: base of the cilia/flagella that anchors it to the cell and controls its movement - has **9+0** structure (9 microtubule triplets, no central pair) cilia are shorter in size than flagella which are longer
58
how do cilia and flagella move?
motor protein **dynein** walks along the microtubules, causing them to bend the bending creates a **back-and-forth beating** in cilia and**wave like motion** in flagella
59
role of centriole in the formation of cilia and flagella?
centrioles form the basal bodies, which provide the template for the "9+2" microtubule structure of axoneme basal bodies help control **number, position, and movement** of cilia and flagella
60
3 functions of cilia (motile) in the body
**1. Respiratory tract**: move foreign particles (dust, mucus, bacteria) out of the airways, helping keep the lungs clean **2. Oviducts (fallopian tubes)**: help move the ovum (egg) toward the uterus for fertilization or menstruation **3. Brain & Spinal cord**: in the fluid-filled brain chambers help with: - producing *cerebrospinal fluid (CSF)* - circulating CSF around the brain and spinal cord to provide protection and nutrients
61
primary cilium + 3 functions
**primary cilium**: single, non-motile cilium found in almost all human cells [only 1 present in all cells] - unlike motile cilia, does not move but works like a sensor for the cell **Functions**: **1. Sensory Organ**: detects signals from the environment and helps cell respond **2. Receives Regulatory Signals**: helps in cell communication by receiving signals that control growth and function **3. Controls Cell Growth & Division**: helps regulate cell differentiation (specialization), cell proliferation (multiplication), and tissue development *crucial for proper development & involved in signaling pathways*
62
2 diseases caused by defects in primary & motile cilia
**1. Polycystic Kidney Disease (PKD)** – Linked to Primary Cilium Defects - kidney cells grow abnormally = fluid-filled cysts in kidneys = kidney enlargement & failure over time **2. Chronic Respiratory Disease** – Linked to Motile Cilia Defects - motile cilia don’t work properly = mucus builds up = chronic infections, coughing, and breathing problems.
63
formation of the mitotic spindle (microtubules & microfilaments)
**Microtubules** → **nuclear division** (separate chromosomes) - *mitotic spindle* which is made of microtubules forms & pulls apart duplicated chromosomes so each daughter cell gets an equal share - start from *centrioles* and are only present temporarily during mitosis **Microfilaments (Actin)** → **cytokinesis ** (split the cytoplasm) - contractile ring made of *actin* (microfilaments) tightens around the middle of the cell, pinching it into 2 daughter cells
64
structure & function of microfilaments
**structure**: made of actin protein that twists into strands (look like 2 strands twisted together) - found in all eukaryotic cells, right beneath plasma membrane **functions**: 1. Cell shape and support 2. Cell movement - involved in **amoeboid movement** (how some cells crawl) 3. Cytokinesis - form **contractile ring** that pinches the cell into 2 4. Intracellular support to move organelles & vesicles inside cell 5. Muscle contraction - works with **myosin to help muscles contract**
65
4 types of human cells that can move on their own **imp viva question**
- sperm (by flagella) - white blood cells (most active crawlers) - fibroblasts (move to damaged area to repair damage) - skin cells *move by amoeboid movement*
66
amoeboid movement **seq**
type of cell movement where a cell crawls by extending parts of its body 4 steps using **microfilaments (actin filaments)**: 1. Extension: *pseudopodia formation (false foot)* 2. Attachment: pseudopodia attaches to a surface using adhesion proteins 3. Contraction & Forward movement: back of cell contract (with help of *actin & myosin*) pulling the cell forward 4. **De-adhesion**: pulling away of rear end from its attachment *entire mechanism is ATP dependent*
67
Microvili + Actin's role
**microvili**: tiny, non-motile, hair-like projections found on the surface of some epithelial cells (cells that line organs) - like intestines, kidneys **main role**: increase surface area + improve absorption of nutrients **role of actin filaments**: each microvillus supported by bundle of actin filaments that run inside it and act as *stiff rods*, preventing microvilli from collapsing or bending too much
68
Which of the following best describes the involvement of actin microfilaments during cytokinesis?
They create a contractile ring to divide the cytoplasm
69
structure & function of intermediate filaments
**structure**: various proteins forming irregular thread-like strands, 7-11 nm diameter - unlike microfilaments and microtubules, intermediate filaments are **more stable** and do not easily assemble/disassemble **functions**: **1. Provide mechanical strength**: help cells resist stretching, compression, & mechanical stress **2. Maintain cell shape**: give structural support to cell, anchor cells, and support *nuclear envelope (lamin intermediate filaments)* **3. Form cell junctions**: keratin filaments in cell-cell adhesion
70
3 examples of intermediate filaments found in various cells
Desmin filaments → Muscle cells Neurofilaments → Neuron cells Keratins → Epithelial cells
71
Intermediate filaments: neurofilaments & keratin
**1. Neurofilaments**: found in axons of nerve cells (neurons) - provide strength & stability to long nerve cell extensions, preventing them from breaking. - imp for maintaining structure & function of neurons **2. Keratin**: (in skin, hair, and nails) - form protective network in skin cells - help create waterproof outer layer of skin - provide strength & durability to skin, hair, and nails, preventing damage from mechanical stress
72
Amyotrophic Lateral Sclerosis (ALS) – Lou Gehrig’s Disease
**cause**: disorganized neurofilaments block axonal transport of crucial materials along microtubular highways, choking off vital supplies from the cell leads to progressive degeneration of motor neurons → gradual loss of control of skeletal muscles (including muscles of breathing) = death *Stephen hawking had this*
73
5 types of cells that exhibit ameboid movement
- white blood cells (tissue macrophages) - fibroblasts (move to repair damage) - germinal cells of skin - embryonic cells (to form babies) - cancer cells (sarcomas- to metastasis to other areas of the body)
74
chemotaxis + 2 types & examples
**chemotaxis**: movement in response to chemical stimuli **positive chemotaxis**: movement *towards* chemical signal - ex. white blood cells move *towards* site of infection in response to chemical signals from damaged tissues or bacteria (**leukocyte chemotaxis**) **negative chemotaxis**: movement *away* from a chemical signal - ex. bacteria moving away from phenol *other examples*: sperm towards egg during fertilization, migration of neurons & lymphocytes in baby development
75
requirements for mechanism of ciliary movement
**1. Availability of ATP**: provides energy for dynein motors to slide microtubules past each other, causing bending **2. Appropriate Ionic Conditions (Ca²⁺ & Mg²⁺)**: Ca²⁺& Mg²⁺ regulate dynein activity and strength of ciliary motion **3. Stroke Cycle of Ciliary Movement**: sudden forward whip-like stroke (effective stroke) & slow backward stroke (recovery stroke)
76
What protein is primarily involved in generating the motive force during ameboid movement?
Actin
77
Primary Ciliary Dyskinesia (PCD)
group of inherited disorders where **cilia do not function properly** due to structural or functional defects **effects**: - airway obstructions & recurrent lung infections due to mucus buildup - dysfunctional flagella causes infertility in males - retinal blindness b/c cilia are involved in photoreceptor cells - cancer (cilia help regulate cell division, defects can lead to uncontrolled growth)
78
The structure supporting the motile cilium includes
11 microtubules, with 9 double tubules around the periphery and 2 single tubules in the center
79
CBL: Kartegener Syndrome + how are cilia affected?
in kartagener syndrome, cilia **dont move (immotile) or dont move well (dysmotile)** - *autosomal recessive inheritance pattern* symptoms: **BDS** **Bronchiectasis** (mucus plus, destruction/dilation of bronchi) **Dextrocardia** (heart is on the right side - bc cilia didnt move in embryogenesis) **Sinusitis** (recurrent sinus infections)
80
investigations that can be carried out to confirm kartagener syndrome
1. **biopsy** from area of the body known to have cilia such as sinus cavities or the airway 2. **blood complete picture** to rule out anemia of chronic infection and active recurrent infection 3. **chest x ray** 4 **HRCT** (type of CT scan to get detailed images of lungs)
81
what is the pattern of ciliary movement?
whip like movement (10-20 times/sec) fast forward and slow backward