C. 4-6

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Last updated 1:50 AM on 6/20/26
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176 Terms

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Metabolism

Sum of all chemical reactions in the body

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Cellular Metabolism

Sum of all chemical reactions occurring in a cell; metabolic reactions usually occur in pathways or cycles.

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Anabolism requires ATP made during Catabolism

Small molecules are built into larger ones; requires energy. Provides materials for maintenance, cellular growth and repair

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Catabolism

Larger molecules are broken down into smaller ones; releases energy

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Smaller molecules are bound together to form larger ones. H2O produced in the process. Used to produce polysaccharides, proteins, triglycerides

Dehydration synthesis (Anabolism)

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Breaks down larger molecules into smaller ones; A T P is produced. Used to DECOMPOSE carbohydrates, proteins, lipids. H2O to split the substances

Hydrolysis (Catabolism)

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Enzymes

Control rates of both catabolic and anabolic reactions. Greatly increase reaction rates

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Enzyme (protein catalysts)/1

Globular proteins that speed up specific chemical reactions. Decreases the energy needed to start a reaction. VERY reusable, because not consumed.

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Each enzyme is highly specific. Its unique shape of its must perfectly fit that substrate, which is why individual steps in a metabolic pathway require distinct enzyme

Enzyme (protein catalysts)/2

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Regulatory enzyme that catalyzes one step of pathway (chemical reaction)

SET RATE for reaction sequence speed.

NEGATIVE FEEDBACK by inhibiting enzyme to stop pathway for homeostasis and optimal efficiency.

Rate-limiting enzyme (1st in reaction sequence) Number of molecules of this enzyme is limited

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Non-protein substance that combines with the enzyme to activate it. Some help fold active site into proper conformation. Some bind enzyme to substrate.

—> A non-protein "helper molecule" that binds to an enzyme to make it functionally active

Cofactor can be ion, element, or small organic molecule (coenzyme)

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<p>Coenzyme</p>

Coenzyme

Organic molecule that acts as cofactor Most are vitamins, which are essential organic molecules that humans must get from their diet

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Denaturation

Inactivation of an enzyme (or any other protein), due to an irreversible change in its conformation. Results in enzyme being unable to bind to substrate

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Energy can't created or destroyed, but can be changed from one form to another

Capacity to change something, or the ability to do work. Heat, light, sound, electrical energy, mechanical energy, chemical energy.

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Energy is transferred to ATP

40% is released as chemical energy. 60% is released as heat; maintains body temperature

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ATP (Adenosine Triphosphate)

Molecule that carries energy in a form the cell can use. Main energy-carrying molecule in the cell; energy from ATP breakdown is used for cellular work

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<p>ATP Consists of 3 portions</p>

ATP Consists of 3 portions

Adenine, Ribose (a sugar), and 3 phosphates in a chain

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When ATP loses terminal phosphate, it become Adenosine Diphosphate (ADP)

ADP can be converted back into ATP by attaching a third phosphate; called phosphorylation, requires energy from cellular respiration.

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Glycolysis (anaerobic), Citric acid cycle (aerobic)

Electron transport chain/oxidative phosphorylation (aerobic)

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Glycolysis and the Electron Transport Chain are stepwise reaction sequences

Citric Acid Cycle occurs in a metabolic cycle in which the final product reacts to replenish original substrate

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Final products of cellular respiration are- Carbon dioxide, Water, ATP (chemical energy, 40%), and Heat (60%)

Cellular respiration need glucose and O2.

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Anaerobic reactions (Glycolysis)

do not require O2, and make little ATP

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Aerobic reactions (Citric Acid, ETC)

require O2, and make most of A T P

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Glycolysis (Cytosal activity) Yields 2 ATP molecules per glucose molecule broken down

Breaks down glucose (6-carbon) into 2 pyruvic acid (3-carbon) molecules. Anaerobic.

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3 Phases of Glycolysis

Phosphorylation of glucose, Splitting glucose, and Production of NADH, ATP, and 2 pyruvic acid

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In presence of O2, NADH and H+ deliver electrons to the electron transport chain, with oxygen as final electron acceptor

Without O2, they go back to Pyruvic

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Aerobic Reactions- In presence of O2, pyruvic acid enters aerobic pathways

Synthesis of Acetyl Coenzyme A, Citric acid cycle, and Electron transport chain

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Aerobic reactions begins with pyruvic acid moving from cytosol to mitochondria

Pyruvic acid is used to produce Acetyl CoA

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Aerobic cellular respiration end products

CO2, H2O, and up to 36 ATP per molecule of glucose

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Begins when acetyl CoA combines with oxaloacetic acid to produce citric acid. Citric acid is changed into oxaloacetic acid through a series of reactions

Citric Acid Cycle repeats as long as pyruvic acid and O2 are available

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1 ATP and 8H+ —> FAD

2 CO2 are produced; enters blood and is exhaled

Each citric acid molecule

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NADH and FADH2 carry hydrogen and high-energy electrons to the

Electron Transport Chain (ETC)

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ETC is a series of enzyme complexes (electron carriers) located

In inner membrane of mitochondria. H2O is formed (oxygen is the final electron "carrier"

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All ATP production in complete oxidation of glucose

2 ATP in glycolysis. 2 ATP in citric acid cycle. 28 in electron transport chain

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DNA (Deoxyribonucleic Acid)

The genetic material. Molecule that stores information on its sequence of nucleotides, that instructs a cell to how synthesize certain proteins

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  • Enzymes

  • Blood proteins

  • tructural proteins of muscle and connective tissue

  • Antibodies • Cell membrane components

The proteins coded for on DNA function as

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Genetic information

Instructions to tell cells how to construct proteins; stored in D N A sequence

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Gene

Sequence of D N A that contains information for making 1 protein

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Genome

Complete set of genetic information in a cell

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Exome

Small portion of the genome that codes for proteins

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Gene Expression

Control of which proteins are produced in each cell type, in what amount, and under which circumstances

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2 chains of nucleotides of double helix. Resembles ladder twisted into a spiral. Backbone of each strand is a sugar-phosphate chain Bases from the 2 complementary strands are C ̶ G, A ̶ T

Structure of DNA

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<p>5-carbon sugar (deoxyribose). </p><p>A phosphate group.</p><p>A nitrogenous base (cytosine, guanine, adenine, or thymine)</p>

5-carbon sugar (deoxyribose).

A phosphate group.

A nitrogenous base (cytosine, guanine, adenine, or thymine)

Nucleotides. Also building blocks of DNA

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Hydrogen bonds break between base pairs. Strands unwind and separate. New nucleotides pair with exposed bases, under direction of DNA polymerase. Other enzymes connect new sugar-phosphate backbone

Steps in DNA replication (interphase)

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RNA differs from DNA in following ways

RNA contains Uracil (instead of Thymine), but the other 3 bases are the same (Adenine, Guanine, and Cytosine).Much shorter than DNA

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<p>Transcription - process of copying a gene's DNA sequence into messenger RNA (mRNA) inside the nucleus</p><p></p><p>***Transcription means to copy something via audio</p>

Transcription - process of copying a gene's DNA sequence into messenger RNA (mRNA) inside the nucleus

***Transcription means to copy something via audio

DNA stores master copy of genetic code, and remains in the nucleus

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Protein synthesis occurs in cytoplasm. mRNA leaves nucleus and binds to ribosome for protein synthesis

At ribosome, the DNA genetic code carried by mRNA, is used to synthesize a protein. Ribosome and tRNA works together to create a protein.

Translation is the process of converting the genetic code (carried by mRNA) into a sequence of amino acids that becomes a protein

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<p>Transcription (In nucleus) </p>

Transcription (In nucleus)

Copying DNA sequence onto an RNA sequence.

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Messenger RNA (mRNA)

The type of RNA that carries genetic code from DNA → ribosome in cytoplasm

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RNA Polymerase

Enzyme that catalyzes the formation of mRNA from the proper strand of DNA

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Each amino acid is specified by a sequence of 3 bases in DNA

Codons

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Aligns amino acids during translation along the mRNA strand on the ribosome. Each ___ contains 3 nucleotide bases, the anticodon, which binds to the complementary codon on the mR N A strand

Transfer RNA (tRNA)

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<p><span>The <strong>Initiation codon</strong>, AUG, codes for Methionine and signals the start of a protein</span></p><p class="MsoNormal"><span>3 codons are <strong>Stop codons</strong>, signaling the end of a protein; these do not have corresponding tRNAs. </span>For each mRNA codon coding for an amino acid</p>

The Initiation codon, AUG, codes for Methionine and signals the start of a protein

3 codons are Stop codons, signaling the end of a protein; these do not have corresponding tRNAs. For each mRNA codon coding for an amino acid

There is corresponding tRNA anticodon

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<p>Steps of Transcription (In the Nucleus). </p><p>1) <span>RNA polymerase recognizes correct strand of DNA to copy</span></p>

Steps of Transcription (In the Nucleus).

1) RNA polymerase recognizes correct strand of DNA to copy

Then RNA polymerase binds to a gene, unwinds the DNA helix, and synthesize a complementary mRNA molecule matching DNA. Termination signals end of gene. Newly created mRNA strand is released. DNA rewinds BACK into double helix

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<p>Ribosome binds to the start codon on mRNA. tRNA matches anticodon to codon, bringing specific AMINO ACIDS TO RIBOSOMES. Growing amino acid chain folds into unique functional protein shape</p>

Ribosome binds to the start codon on mRNA. tRNA matches anticodon to codon, bringing specific AMINO ACIDS TO RIBOSOMES. Growing amino acid chain folds into unique functional protein shape

Translation (In the Cytoplasm)

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Mutations occur when bases are changed, added, or deleted

Changes in the DNA sequence

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Spontaneous Mutations

due to insertion of unstable base into DNA sequence

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Induced Mutations

due to exposure to mutagens, chemicals, or radiation that cause mutation

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Many mutations affect health, by changing the amino acid sequence, resulting in a nonfunctional

Sickle cell disease is caused by a single nucleotide substitution; this causes production of abnormal hemoglobin, which causes change in shape of red blood cells, in low-oxygen conditions, and extreme pain

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Since often 2 to 4 codons specify the same amino acid, some mutations changing the third base of a codon would result in…nothing happening to the protein.

  • If one copy is mutated, the other copy may provide enough of gene’s normal function to maintain health.

DNA Repair correction of a mismatched nucleotide by a Repair Enzyme.

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Epithelial (Protection, secretion, absorption, excretion)

Cover body surface, cover and line inernal organs, compose glands. Lack blood vessels, cells readily divide, cells are tightly packed

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Simple Squamous (Diffusion, Filtration)

Alveoli, capillaries, blood vessels. Lines blood and lymphatic vessels.

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Simple Cuboidal (Secretion, Absorption)

Kidney tubules, ovary surface, thyroid follicles, and secretory portions of small glands

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Simple Columnar (Absorption, Secretion, Excretion)

Small intestine, stomach, uterine tubes (ciliated), bronchioles (ciliated)

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Pseudostratified Columnar (Mucus Secretion, Mucus Propulsion)

Nasal cavity, trachea, bronchi. Nuclei at two or more levels. Cell reach basement membrane. Cilia & goblin cell.

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Stratified Squamous (Protection) - Nuclei at two or more levels.

Skin, oral/esophagus, anal, vagina. Outermost cells are squamous, deeper cells are cuboidal.

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Stratified Cuboidal (Protection)

Sweat gland ducts, mammary gland ducts, salivary gland ducts, and pancreas.

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Stratified Columnar (Protection, Secretion)

Parts of male urethra, vas deferens, salivary glands. Cube-shaped cells in deeper layers

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Transitional (Stretching, Distension)

Urinary bladder, ureters, parts of urethra

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Connective (Bind, support, protect, fill spaces, store fat, produce blood cells)

Widely distributed throughout the body. Mostly have good blood supply, cells are farther apart than epithelial cells, with ECM in between

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Areolar (Wraps, Cushions, Binds Tissues)

Beneath epithelia, around organs, papillary layer of dermis. Collagen, elastic, and reticular fibers.

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Adipose (Energy Storage, Insulation, Protection)

In hypodermis, around kidneys and eyes. Fat-storing cells (adipocytes)

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Specialized CT

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Hyaline cartilage CT

Ends of bones, nose, and rings in walls of respiratory passages

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Elastic cartilage CT

External Ears and Larynx.

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Fibrocartilage

Between bony parts of spinal column, parts of pelvic girdle, and knee

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Bone

Cells in solid matrix. Supports, protects, provides framework. Bones of skeleton, middle ear

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Blood

Cells and platelets in fluid matrix. Transports gases, defends against disease, clotting. Throughout the body in a closed system of blood vessels and heart chambers

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Dense Regular CT (Strong Attachment)

Tendons, ligaments. Parallel collagen fibers; resists pulling in one direction.

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Dense Irregular CT (Strength, Structural Support)

Dermis of skin, organ capsules. Collagen fibers in every direction for PULL resistance.

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Elastic CT (Stretch and Recoil)

Walls of large arteries, vertebral ligaments. Abundant elastic fibers

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Muscle (Movement)

Attached to bones, in the walls of hollow internal organs, heart. Able to contract in response to specific stimuli

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Skeletal Muscle (Attached to bones)

Striated, voluntary, multinucleated; responsible for body movement, posture, and heat production.

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Cardiac Muscle (Heart wall)

Striated, involuntary, branching cells with intercalated discs; pumps blood throughout the body.

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Smooth Muscle (Walls of stomach, intestines, bladder, blood vessels)

1) Central nucleus and short spindle-shaped cells

Non-striated, moves substances through hollow organs and regulates vessel diameter.

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Unicellular glands

A single secretory cell. Mucous-secreting cell

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Multicellular glands

Glands that consist of many cells

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Simple glands

Glands that communicate with the surface by means of ducts that DONT BRANCH before reaching the secretory portion

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<p>Simple tubular gland</p>

Simple tubular gland

Straight tube-like gland that opens directly onto surface. Intestinal glands of small intestine

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<p>Simple branched tubular gland</p>

Simple branched tubular gland

Branched, tube-like gland; duct short or absent. Gastric glands

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<p>Simple coiled tubular gland (Merocrine)</p>

Simple coiled tubular gland (Merocrine)

Long, coiled, tube-like gland; long duct.

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<p>Simple branched alveolar gland</p>

Simple branched alveolar gland

Secretory portions of gland expand into saclike compartments along duct. Sebaceous gland of skin

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Nervous (Conduct impulses for coordination, regulation, integration, and sensory reception)

Brain, spinal cord, nerves. Cells communicate with each other and other body parts

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<p>Neurons (Brain, spinal cord, peripheral nerves)</p>

Neurons (Brain, spinal cord, peripheral nerves)

Specialized cells that conduct nerve impulses; responsible for communication, sensory reception, and motor control.

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<p>Neuroglia/Glial Cells (Brain, Spinal Cord, Peripheral Nerves)</p>

Neuroglia/Glial Cells (Brain, Spinal Cord, Peripheral Nerves)

Support, protect, and nourish neurons, maintaining the nervous system.

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Hyaline Cartilage (Support, Reduce Friction) VERY SMOOTH matrix

Nose, trachea, larynx, ends of long bones. More flexible bones. Most common cartilage

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<p>Elastic Cartilage (Flexible Support)</p>

Elastic Cartilage (Flexible Support)

External ear, epiglottis. Contains many elastic fibers

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<p>Fibrocartilage (Shock Absorption) STRONGEST cartilage</p>

Fibrocartilage (Shock Absorption) STRONGEST cartilage

Intervertebral discs, menisci of knee, pubic symphysis. Thick collagen fiber

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Reticular CT (Supportive Framework)

Liver, spleen, lymph nodes. Network of reticular fibers supporting other cells

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Tight junctions

Close space between cells by FUSING cell membranes. Cells that line the small intestine