1these allow proteins in the membrane to interact with other cells
roups
carbohydrates
2these allow proteins in the membrane to have more motility

cholesterol
3what are the different types of integral membrane proteins?

pumps, channels, receptors, linkers, enzymes, structural
4move substances against the concentration gradient, integral membrane protein

pumps
5favorable membrane transport, energy npt required for things to move across this thing

channels
6rigid scafolding so cells dont move freely along the medium, integral membrane proteins

linkers
7diffusion with no mediation needed
EX; uncharged small nonpolar molecules

simple diffusion
8used in active (pumps) or passive transport, highly selective for what they are moving

carrier proteins
9ligand gated or voltage gated, regulated by membrane potentials

channel proteins
10phrase for favorable (conc)
down conc. gradient
11phrase for nonfavorable (conc)
up conc gradient
12types of endocytosis

pinocytosis, phangocytosis, receptor mediated endocytosis
13types of exocytosis

constitutive: constant
regulated: needs signaling to occur
14cell drinking, nonspecific, small proteins and fluids

pinocytosis
15Engulf cell debris and bacteria
Requires rearrangement of the actin cytoskeleton
Form phagosomes

phangocytosis
16steps to receptor mediated endocytosis

1) cargo protein binds to cargo receptor as adaptin also binds to intracellular cargo receptor
2) clarthrin binds to adaptin, coated pin forming
3) coated pit formed and vessel invaginates
4) vessel completely invaginates and moves into the cell
5) vessel begins uncoating as adaptin/clarthrin bindings break off
6) uncoated vesicle

17what is the functio and pH of early endosomes
sory and recycle proteins; 6.2
18what is the function and ph of late endosomes

pre lysosomes, some sorting still occurs; 5.5
19what is the structure and ph of lyososomes

degradation, ph 4.7
20what 4 pathways lead to intracellular digestion in lysosomes?

receptor mediated endocytosis, pinocytosis, phangocytosis, autophagy
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26Loss of vision & hearing, muscle atrophy from loss of nervous tissue, early death (< 5y)
Tay Sachs
27what enzyme is deficient in tay sachs
hexosaminidase
28what is the function of hexosaminidase (tay sachs)
Gm2 ganglioside breakdown, builds up in lysosomes and neuronal cells when deficient
29Skeletal abnormalities, hepatomegaly, intellectual disability, early death (< 8y)
I-cell disease
30what enzyme is deficient in I cell disease?
N-acetylglucosaminyl-1-phosphotransferase
31what is the function of N-acetylglucosaminyl-1-phosphotransferase?
lysosomal hydrolases are not phosphorylated and get secreted instead leading to multiple substances accumulating in the lysosomes
32Hepatosplenomegaly, neurodegeneration, progressive wasting due to sphingomyelin accumulation; early death (< 3y)
Niemann-Pick (type A)
33Sphingomuelinase
what enzyme is deficient in niemann pick type a
34what happens with sphingomuelinase deficiency? (niemann pick type a)
sphingomyelin accumulates
35Affects the spleen, liver, lungs, bone marrow
Gaucher
36what enzyme is effected in gaucher?
B glycocerebrosidase
37what does a deficiency in B glucocerebrosidase cause?
glucosyleramide accumulaes in macrophage (monocyte system)
38contains enzymes that break down H2O2
peroxisomes
39functions of peroxisomes
β-oxidation of fatty acids
Detoxification of ethanol
Synthesis of plasmalogens

40what is the deficiency in zellweger syndrome?
Mutations in at least 12 genes ID’d, code for peroxins
41what does the mutation in zellweger syndrome cause?

reduce myelin synthesis and loss of white matter
42Rough ER function?

synthesis of secreted and membrane proteins
43smooth ER function
lipid metabolism
detoxification
steroid synthesis

44Golgi function?

post translational modification, sorting, pavkaging of proteins
45what are the types ofnonliving inclusions

Secretory granules
Stored energy (e.g., glycogen and fat)
Pigments (e.g., hemoglobin and melanin)
46Cytoskeleton parts
microtubles, actin, intermediate filaments
47what happens if you have more GTP than GDP
polymerization
48functions of microtbles

Vesicular transport
Movement of cilia and flagella
Alignment, separation of chromosomes during cell division
50movement - to +
kinesins
51align mitotic spindle during cellular division
centrosomes
52Central point of MTOC assembly
9 sets of microtubule triplets
centrosome is 2 of these

centrioles
53microtuble disorder
kartagener syndrome
54what happens in kartagener syndrome
immobility of cilla and infertility
55what are the chemotherapy drugs? (microtuble drugs)
taxol (paclitaxel) and vinblastine/vincristine
56prevents depolymerization microtubles
taxol (paclitaxel)
57inhibits formation of mitotic spindke for cell division
vinblastine/vincristine
58actin functions (x5)
Cell shape/structure
Microvilli
Anchorage and movement
Extension of cell processes
Locomotion
59prevents depolymerization by binding to F actin
phalloidin
60prevents polymerization of actin; this inhibits lymphocyte migration, phangocytosis, and cell division
cytochalasin B and D
61intermediate fillaments function
structural role
62what are the types of intermediate filaments
Keratins
All epithelial cells
Vimentins
Fibroblasts, neurons
Neurofilaments
Neurons
Lamins
Most differentiated cells, all nucleated cells
63intermediate filament disorders
alcohol liver cirrhosis: keratin accumulation as mallory bodies, alzheimers: neurofilaments
64function of nucleolus

rRNA synthesis
65scaffolding for the chromosomes and the nuclear pores
nuclear lamina
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69impaired nuclear lamina disorders (x2)
progeria, emery-dreifuss muscular dystrophy
70what gene is mutated in progeria
lamin A/C gene
71what happens with a lamin A/C gene mutation (progeria)
splicing of lamina A mRNA, lamin A tight;y associated with nuclar memnrane si there are problems with chromatin scaffolding in nucleus
72what is mutated/effected n emery dreifuss muscular dystrophy
multiple genes, affects the nuclear envelope; muscle weakness and stiff joints (onset age 10)
73X chromosome is repressed and stays tightly condensed

Barr body
74what happens during the interphase phases?
G1: proteins neeed for DNA synthesis
S: DNA synthesis
G2: growth and reorganization
75what is the Go phase
cells are stable and nondividing
76what is the Gtd phase
permanent nondividing cells phase
77what regulates the cell cycle?

cyclins which activate cyclin dependent kinases at checkpoint regulators
78accidental cell death where the cell lyses and swells
necrosis
79basophilic dye
hematoxylin
80what do basic dyes color
heterochromatin and nucleoli
cytoplasm
ECM
82what does acidophilic dye dye?
cytoplasmic filaments
Intracellular memnrane filamennts
extracelular fibers
83where is epithelium not found
articular cartilage, anterior surface of iris, enamel of teeth
84where is pseudostratified epithelium found?
airway and mail reproductive tract
85where is transitional epithalium found
urinary system, bladder, urethra
86what is the issue with transition zones like the gastro esophageal junction?
cancers (metaplasia)
87Finger-like projections involved in absorption
“brush border”
Complex cytoskeleton anchored to terminal web; core of actin filaments – contractile properties

microvilli
88Unusually long, immotile microvilli (see internal structure)
Limited to epididymis, ductus deferens, cochlear & vestibular hair cells
stereocilia

89cilia types
motile and flagella (9+2): trachea, bronchi, oviducts
primary cilia
nodal cilia
90what is the lateral domain made up of (x2)
terminal bar, junctional complex, lateral folds
91what is the terminal bar/junctional complex made up of?
occluding tight junctions (linked to actin) which seperate cellular tissue
anchoring junctions: zona adherins (actin), macula adherins (intermediate filaments)
communicating junctions (gap)
92what is the basal domain made up of?

basement membrane
cell to ECM junctions: focal adhesions (actin), hemidesmosome (intermediate filaments)
basal cell membrane foldings
93what are the two types of endocrine glands
cord and clump, follicle
94what gland?

cord and clump
95what gland?

follicle
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103purple in image (exocrine gland)

nuclei
104light pink in photo (exocrine )

mucous secreting exocrine glands
105dark pink in photo (exocrine)

serous secreting exocrine glands
106what type of exocrine gland

mixed, has both serous and mucous secreting glands
107Thin filaments muscles?
actin
108thick filaments muscle
myosin II
109three typoes of striated muscle
skeletal, visceral striated, cardiac
110may have attachments to bone but is associated with the gut tube, same histo as skeletal but different embryology
visceral striated
111where is smooth muscle found
viscera: blood/lymph vessels, organs, glands
112muscle fibers arise from aggregations of ________________ these cells fuse to form a ____________________ muscle fiber

myoblasts; multinucleated
113means many nuclei, this is what muscle fibers are
syncythium
114strength of muscle depends on this
number of fibers
115attach muscle to bone
tendons
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121black arrow?

epimysium
122yellow arrow?

perimysium
123blue arrow?

endomysium
124different fiber types/colors are attributed to (x3)
Succinic dehydrogenase
NADH-TR
Myoglobin
125what are the characteristics of white/fast glycolitic/type IIb fibers
low succinate dehydrogenase, atpase
less extensive blood supply
fewer mitochondria
adapted for rapid and powerful cotraction
126what are the characteristics of red/slow twitch/aerobic/type I fibers
smaller, extensive blood supply, many mitochondria and myoglobin
for prolonged and continued actvity
127invaginatuons of the plasma membrane (sarcolemma) used to have SR closer to membrane to speed up muscle contractions 9easier ease of access for Ca2+

transverse tubles
128contractile unit of muscle fbers
myofibrils
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136modified smooth ER, is arranged around myofibers; serves as a reservoir for Ca++
sarcoplasmic reticulum
137tissue type? whats happening here?

skeletal; muscle atrophy
138intrafusal fiber types

muscle spindles, golgi tendon
139what is this?

muscle spindle
140these can regenerate skeletal muscle fibers to a minimum capacity
satellite cells
141what is this muscle tissue? specifics

cardiac muscle; coducting fibers
142how many T tubles per SR in cardiac? in skeletal?
1; 2
143what do cardiac cells do in repair?
scar tissue; limited repair
144smooth muscle cells regeneration
can regenerate; pericytes
145dense bodies are a characteristic of this muscle type
smooth
146what fibers make up ECM

collagen
reticular
elastic
147what ground substances make up ECM

glycoproteins (fibronectn and laminin), glycosaminoglycans (sulfate), proteoglycans
148what is made up of type 1 collagen?
bone, skin, tendons, ligaments
149what is made of type 2 collagen

hyaline cart
150what is made of type 3 collagen

reticular fibers
151what is made og type 4 collagen
basement mambrane
152what forms collagen I fibers

fibroblasts and osteoblasts
153where can you find reticular fibers?

adipocytes, muscle cells, small blood vessels hemopoietic and lymphatic tissues
154what type of stain?

silver salts
155what forms reticular fibers?

fibroblasts, smooth muscle cells, schwann cells
156where are elastic fibers found?

elastic cartilage, elastc arteries, elastic ligaments
157what stain?

resorcin fuchsin
158what makes elastoc fibers?

fibroblasts and smooth muscle cells
159what makes up elastic fibers?

Elastin (central core)
Fibrillin microfibrils around the core embedded into elastin
160what is the deficiency in marfan syndrome

mutation in fibrilin 1 gene, fibil imp for maintaining elastic fibers
161what is the deficiency/issue in ehlers danlos syndrome?

mutation in genes affecting collahen polypeptide chains
162what is the issue/deficiency in osteogenesis imperfecta

type 1 collagen mutation: less severe
type II collagen mutation: small and fragile rib cage
163Star or spindle shaped cells
Pluripotential – capable to form various cell types
In adult, they are located usually around the vessels

mesenchymal cell
164where are mesenchymal cells located?

around the vessels
165what can mesenchyme cells form (x5)
chondroblasts, lipoblasts, fibroblasts, osteoblasts, myoblasts
166what are the funct of fibroblasts
synthesize fibers and ground substances, protein synthesis
167what are the functions of myofibroblasts
regulating the shape and empotying f glands and wound contraction and closure

168where are myofibroblasts located

loose connective tissue
169Numerous mitochondria
Characteristic for newborns – rapid energy release

brown adipose
170macrophages function
Phagocytic cells derived from blood monocytes - garbage collectors of the tissue

171where are mast cells located

small vessels in connective tissue, capsules of organs
172fx mast cells

anaphylactoc oversensitive reactions
173what do heparan sulphate and heparin do in mast cells
block coagulkation, resp for basophilic apprearance
174what are histamine and SRS-A resp for in mast cells
vasodilation, edema
175what are ECF and NCF resp for in mast cells
celll attraction
176what are the different types of lymphocytes and where do they differentiate?

T lymphocytes (differentiating in the thymus) – 60-80 %
B lymphocytes (differentiating in the bone marrow) – 20-30 %
NK (natural killer) cells – 5-10% (bone marrow)
177what are plasma cells derived frpom?

B cells
178what are plasma cells fxn

antibody producing
179Capable of migration
Granules –small, purple, barely visible in the light microscope
Nucleus multilobed (thus also called polymorphs)

neurotrophils
180Named after the large eosinophilic granules in the cytoplasm
Typically bilobed nucleus

eosinophils
181Large basophilic granules in the cytoplasm
Nucleus obscured by the granules
Closely related to mast cells of the connective tissue

basophils
182what are the types of embryonic connective tissue (x2)
mesenchyme, mucous connective tissue
183where can you find mucous connective tissue

umbilical cord
184what cells are present in mucous connective tissue

fibroblasts and mesenchymal cells
185Primitive pluripotent connective tissue – capable of turning into other tissue types
Cells: pluripotential mesenchymal cells
Cells are more closely packed than in Wharton’s Jelly

mesenchyme
186Few fibroblast
Little ground substance
Large amount of collagen fibers between them

Dense connective tissue
187Fibers are arranged in parallel array
Present in tendons, aponeuroses and ligaments

dense regular connective tissue
188Fibers are arranged in bundles running in every direction
Present in the submucosa of the hollow organs – connecting the mucous membrane to the underlying muscle layer

dense irregular connective tissue
189Loosely arranged fibers and cells
Found mostly beneath the epithelia (layer is called lamina propria mucosae)
Contains blood cells (migrated from local blood vessels)
In inflammation it can undergo significant swelling

loose connective tissue