Cell Physiology Flashcards

1
Q

What percentage of body weight is total body water in a dog, and how is it distributed?

A

Total body water in a dog is approximately 60% of body weight.
It is distributed as 1/3 extracellular fluid (ECF) and 2/3 intracellular fluid (ICF).

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2
Q

Define homeostasis

A

Homeostasis is the maintenance of a nearly constant internal environment.

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3
Q

What are the key differences in ion composition between extracellular fluid and intracellular fluid?

A

Extracellular fluid contains mainly Na, Cl, and HCO₃, Intracellular fluid contains primarily K, Mg, and PO₄.

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4
Q

Describe negative feedback in body control systems with an example.

A

Negative feedback occurs when an increased value triggers a compensatory mechanism that decreases the value (negative to the initiating stimulus).

Example: When arterial blood pressure rises, baroreceptors signal to lower it back to normal range.

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5
Q

What is the formula for calculating the gain of a control system?

A

Gain = Correction/Error
The gain determines the effectiveness with which a control system maintains constant conditions.

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6
Q

When can positive feedback be useful in physiological systems?

A

Positive feedback, though potentially dangerous (creating “vicious cycles”), can be useful in processes such as blood clotting, uterine contractions during childbirth, and nerve signal generation.

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7
Q

What are the two main systems for protection of the body

A

Immune system and integument

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8
Q

What are the two main mechanisms for regulation of body functions

A

nervous system and hormones

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9
Q

What are structural proteins

A

Long filaments often forming microtubules to provide cytoskeleton of cellular organelles

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10
Q

What are functional proteins

A

Tubular globular forms that act as enzymes, often mobile; can adhere to cell membrane to catalyse reactions

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11
Q

What is the composition of the cell membrane

A

55% protein, 25% phospholipid, 13% cholesterol, 4% other lipid, 3% carbohydrates

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12
Q

What substances can easily penetrate the lipid bilayer

A

Fat-soluble substances (O₂, CO₂, alcohol)

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13
Q

What is glycocalyx and what are its functions

A

A loose coat of proteoglycans around the cell, formed by glycoproteins or glycolipids that protrude from the cell surface

Repels negatively charged objects, attaches cells together, serves as receptors for hormone binding, activates intracellular enzymatic reactions, and participates in immune reactions

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14
Q

What is the difference between rough ER and smooth ER

A

Rough ER has ribosomes attached to its outer surface and is involved in protein synthesis;
Smooth ER lacks ribosomes and is involved in lipid synthesis (mainly cholesterol and phospholipids)

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15
Q

What is the function of the Golgi apparatus

A

It processes vesicles from the ER to form lysosomes, secretory vesicles, and other cytoplasmic components

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16
Q

What are lysosomes

A

Vesicles that break off from the Golgi apparatus, containing hydrolase enzymes that function as the cell’s digestive system

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17
Q

What do peroxisomes contain

A

Oxidases, hydrogen peroxide, and catalase

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18
Q

What is the main function of mitochondria

A

Oxidation of nutrients to form CO₂, H₂O, and energy, which is used to form ATP

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19
Q

What is the function of microfilaments

A

They provide elastic support and enable muscle contraction (actin/myosin)

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20
Q

What is the function of intermediate filaments

A

They provide strength and support to the cell

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21
Q

What is the function of microtubules

A

They provide strength and structure to the cytoskeleton, and form centrioles and mitotic spindles

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22
Q

What is the function of the nucleus

A

It serves as the control centre for cell growth, maturation, replication, and death

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23
Q

What are nucleoli

A

Structures within the nucleus (without a membrane) that contain large amounts of RNA and proteins, involved in ribosome formation

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24
Q

What is pinocytosis

A

Ingestion of minute particles that occurs continuously in the cell membrane

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25
Q

What is phagocytosis

A

Ingestion of large particles, bacteria, or whole cells by specialized cells like macrophages and some leukocytes

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26
Q

What happens in a digestive vesicle

A

Lysosomes empty hydrolases into pinocytic vesicles, forming digestive vesicles where hydrolysis products can diffuse through the membrane

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27
Q

What is autophagy

A

The process where organelles are transferred to lysosomes by autosomes, which fuse with lysosomes to form autophagosomes, allowing nutrients to be reused by the cell

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28
Q

What antibacterial agents do lysosomes contain

A

Lysozyme (dissolves bacterial cell walls),
Lysoferrin (binds iron to prevent bacterial growth),
and an acidic pH that activates hydrolases and inactivates bacterial metabolism

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29
Q

What is ATP composed of

A

A nitrogenous base (adenine), a pentose sugar (ribose), and three phosphate radicals

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30
Q

What percentage of cellular ATP is formed in mitochondria

A

95%

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31
Q

What are three major uses of ATP in cellular function

A

Transport of substances through cell membranes,
Synthesis of chemical compounds,
Mechanical work

32
Q

What is ameboid movement and what cells use it

A

A form of cell movement where new membrane formation causes pseudopodia to project forward, followed by receptor binding and actin filament contraction to pull the cell forward

White blood cells, tissue macrophages, fibroblasts, embryonic cells, and neoplastic cells

33
Q

What is chemotaxis

A

The process that initiates cell movement toward (positive) or away from (negative) a chemical substance

34
Q

What is the structure of cilia

A

11 microtubules - 9 doubles and 2 single in the centre, which are outgrowths of the basal body

35
Q

What are the two types of cilia

A

Motile cilia (with whip-like motion) and non-motile cilia (serving as sensory antennae)

Motile cilia - Respiratory airways and fallopian tubes

36
Q

What is required for ciliary movement

A

ATP (causes dynein protein to project), calcium, and magnesium

37
Q

What are the basic chemical components of an acidic nucleotide in DNA?

A

Phosphoric acid, deoxyribose sugar, and a nitrogenous base (either purine or pyrimidine)

38
Q

What are the two types of nitrogenous bases in DNA, and which bases belong to each type?

A

Purines (adenine, guanine) and pyrimidines (thymine, cytosine)

39
Q

What is the base pairing rule in DNA?

A

Adenine always pairs with thymine, and guanine always pairs with cytosine

40
Q

What is a triplet in genetic code?

A

A triplet is a sequence of three bases that forms a code word, with each triplet responsible for coding a specific amino acid

41
Q

How does RNA differ from DNA?

A

RNA uses ribose (contains extra hydroxyl ion) instead of deoxyribose,
RNA uses uracil instead of thymine as a pyrimidine base

42
Q

What are the four nucleotides in RNA?

A

Adenine (A), uracil (U), cytosine (C), and guanine (G)

43
Q

How are RNA nucleotides activated?

A

By RNA polymerase adding two extra phosphate radicals to form triphosphates, using ATP to add new nucleotides to the end of the developing chain

44
Q

What is Pre-mRNA and what are its components?

A

Precursor messenger RNA is a large single strand of RNA processed in the nucleus to form mRNA
it includes introns (removed by splicing) and exons (retained in mRNA)

45
Q

What is the function of small nuclear RNA (snRNA)?

A

It directs the splicing of pre-mRNA to form mRNA

46
Q

What is the function of messenger RNA (mRNA)?

A

It carries genetic code from the nucleus to the cytoplasm to control protein formation

47
Q

How does transfer RNA (tRNA) function in protein synthesis?

A

tRNA transports activated amino acids to ribosomes

it recognizes specific codons on mRNA through its anticodon, delivering the appropriate amino acid to the right place in the protein chain

48
Q

What is the structure and function of ribosomal RNA?

A

Ribosomal RNA, along with 75 different proteins, forms ribosomes where proteins are assembled; it works in association with mRNA and tRNA

49
Q

What is microRNA (miRNA) and its function?

A

miRNA consists of single-strand RNA molecules that regulate gene transcription and translation

It binds to mRNA, causing repression of translation or degradation of the mRNA

50
Q

What is transcription?

A

The process where DNA code is transferred to RNA

51
Q

What are the main steps in RNA chain assembly during transcription?

A

1) RNA polymerase attaches to the promoter on DNA
2) DNA unwinds and separates
3) Polymerase moves along and adds RNA nucleotides to the chain
4) Chain terminating sequence causes polymerase to break away, and the new RNA chain separates from DNA

52
Q

What are polyribosomes?

A

Clusters of ribosomes (3-10) attached to the same mRNA

53
Q

What is the TATA box and its function?

A

The TATA box is a sequence of bases (TATAAA) in the basal promoter that serves as the binding site for TATA-binding protein and transcription factor IID complex

RNA polymerase must bind to the basal promoter before it can synthesize RNA.

54
Q

What are enhancers in gene regulation?

A

Enhancers are regions of DNA that can bind to transcription factors and can be located far from the gene they regulate

55
Q

What are insulators in genetic regulation?

A

Insulators are gene sequences that provide a barrier between active and suppressed genes; they can be modulated by DNA methylation

56
Q

What are histones

A

DNA is wound around histone proteins in chromosomes.

When wound tightly, DNA cannot form RNA; specific mechanisms can unwind selected areas to allow gene expression

57
Q

How does DNA replication differ from RNA transcription?

A

In DNA replication: both DNA strands are replicated, replication occurs from end to end, DNA polymerase (not RNA polymerase) is used, and DNA ligase bonds nucleotides together

58
Q

What is the role of DNA helicase in replication?

A

DNA helicase enzymes break down hydrogen bonds between base pairs to allow ‘unzipping’ and replication fork formation

59
Q

Why is DNA replication only in the 5’ to 3’ direction?

A

DNA polymerase can only add nucleotides to the 3’ end of a growing DNA strand

60
Q

What are Okazaki fragments?

A

Short, newly synthesized DNA fragments that are formed on the lagging strand during DNA replication and later joined by DNA ligase

61
Q

What is the role of topoisomerase in DNA replication?

A

Topoisomerase breaks phosphodiester bonds in the DNA backbone to prevent overwinding in the helix in front of the replication fork

62
Q

What are the main phases of mitosis?

A

Prophase, prometaphase, metaphase, anaphase, and telophase

63
Q

What happens during prophase?

A

The spindle forms and chromosomes condense

64
Q

What occurs during metaphase?

A

Chromatids are pulled tightly by attached microtubules to the center of the cell, forming the equatorial plate of the mitotic spindle

65
Q

What happens during anaphase?

A

Chromatids are pulled apart at the centromere, separating 46 chromatids into 46 daughter chromosomes, with one set pulled toward each aster

66
Q

What occurs during telophase?

A

The two sets of daughter chromosomes are pushed completely apart, the mitotic apparatus dissipates, new nuclear membranes form, and the cell pinches in two due to a contractile ring of microfilaments

67
Q

What are telomeres and their function?

A

Telomeres are regions of repetitive nucleotide sequences at the end of chromosomes that prevent degradation of chromosomes and act as a protective cap to prevent loss of genome

68
Q

How do telomeres relate to cell aging?

A

When telomeres shorten to a critical length, chromosomes become unstable and cells die; telomere erosion is caused by cell division, oxidative stress, and inflammation

69
Q

What is the role of telomerase?

A

Telomerase is an enzyme that adds bases to the ends of telomeres in certain cells like stem cells

In cancer cells, telomerase activity is activated and allows uncontrolled replication

70
Q

What is apoptosis?

A

Programmed cell death involving a proteolytic cascade that causes cell shrinkage, condensation, cytoskeleton disassembly, and membrane changes to allow phagocytosis by macrophages

71
Q

How is apoptosis initiated?

A

By activation of caspases, which are protease enzymes stored in cells as inactive procaspases

72
Q

How does apoptosis differ from necrosis?

A

In apoptosis, cells undergo programmed death

In necrosis (due to injury), cells swell and burst, causing inflammation and injury to nearby cells

73
Q

What are proto-oncogenes? What are oncogenes?

A

Genes that code for proteins controlling cell adhesion, growth, and division

when mutated, they become oncogenes responsible for cancers

74
Q

What are tumor suppressor genes?

A

Anti-oncogenes that suppress the activation of specific oncogenes

75
Q

Why do only a small proportion of mutated cells cause cancer?

A

Mutated cells often have less survival capacity,
Most still have normal feedback control to prevent excessive growth,
Many are destroyed by the body’s immune system

76
Q

What gives cancer cells their invasive characteristics?

A

Cancer cells don’t respect usual cellular growth limits,
Less adhesive than normal cells,
Produce angiogenic factors that promote blood vessel growth and nutrient supply

77
Q

How do cancer cells kill?

A

By competing for nutrients and disrupting vital organ function