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Test Bank for Color Textbook of Histology, 3rd Edition: Leslie P. Gartner download pdf full chapter
Test Bank for Color Textbook of Histology, 3rd Edition: Leslie P. Gartner download pdf full chapter
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Gartner & Hiatt: Color Textbook of Histology, 3rd Edition
Test Bank
Chapter 2 – Cytoplasm
MULTIPLE CHOICE
a. glycerol
b. phosphate group
c. cholesterol
d. integral proteins
e. peripheral proteins
Explanation:
The answer is c. Cholesterol decreases membrane fluidity. The polar heads of
phospholipids molecules are composed of glycerol, to which a positively charged
nitrogenous group is attached by a negatively charged phosphate group. Unsaturated fatty
acyl molecules increase membrane fluidity. Integral and peripheral proteins do not have
an effect on membrane fluidity.
2. A patient suffering from asthma has difficulty breathing and is treated with albuterol, a
drug that relaxes bronchiolar smooth muscles. Albuterol acts as a(n)
Explanation:
The answer is d. Albuterol is an agonist that acts on β2-adrenergic receptors that are
located mainly on the cell membranes of bronchial tissues and, therefore, do not have
many side effects. If it were an antagonist, then it would cause smooth muscle
constriction.
Test Bank 2
3. A patient suffering from asthma has difficulty breathing and is treated with albuterol
and ipratropium, drugs that relax bronchiolar smooth muscles. Ipratropium acts as a(n)
Explanation:
The answer is a. Ipratropium is a cholinergic receptor antagonist and interferes with the
binding of acetylcholine, a neurotransmitter, to its receptor sites on the cell membrane,
thus preventing the contraction of bronchiolar smooth muscle. The two drugs are used in
combination agonist-antagonist therapy to have the desired effect of maintaining an open
airway.
4. A 9-month-old female Jewish baby, whose parents were born in Poland, is seen by her
pediatrician because of neurologic problems, including generalized paralysis and
blindness. The pediatrician should suspect that the child is suffering from
a. spina bifida
b. cranial nerve X (vagus nerve) disorder
c. Tay-Sachs disease
d. Fabry’s disease
e. Refsum’s disease
Explanation:
The answer is c. Tay-Sachs disease affects mostly children of Eastern European Jewish
ancestry as well as certain families in Lousiana of Cajun ancestry. Children suffering
from this lysosomal-storage disease cannot catabolize GM2 gangliosides that accumulate
in their lysosomes, and the enlarged lysosomes interfere with cell function. The
interference is most problematic in the neurons of the central nervous system and causes
death by the third year of life. Neither spina bifida nor vagus nerve disorders would cause
generalized paralysis or blindness. Fabry’s disease, although a lysosomal-storage
disorder, is due to an X chromosomal defect and affects only males. Refsum’s disease is
due to the accumulation of phytanic acid, a by-product of chlorophyll metabolism, and
affects older children who already eat fresh fruits and vegetables.
5. Acid hydrolases are synthesized on the rough endoplasmic reticulum and are delivered
to the Golgi complex to be packaged and distributed to their final destination. In patients
whose protooncogenes have mutated to form ras protein–related products known as ADP-
ribosylation factor (ARF), this factor may interfere with
d. clathrin synthesis
e. clathrin assembly
Explanation:
The answer is b. Delivery of proteins manufactured on the rough endoplasmic reticulum
to the Golgi complex is accomplished in COP-II coated vesicles. ARF catalyzes the
assembly of COP-II molecules to form coatomer on the cytoplasmic aspect of these
transfer vesicles. Synthesis of COP-II proteins as well as the disassembly of the coatomer
are not influenced by ARF. Clathrin coats mediate the endocytotic pathway as well as the
pathway that leads away from the trans Golgi network.
6. Patients with sickle cell anemia possess hemoglobin-s, a mutated form of hemoglobin.
Hemoglobin-s is
Explanation:
The answer is a. Hemoglobin, whether normal or mutated, is present freely in the cytosol;
therefore, it is synthesized on free ribosomes. Only proteins that are to be packaged are
synthesized on the rough endoplasmic reticulum. Because hemoglobin is not packaged, it
does not enter the Golgi apparatus.
7. A neonatal baby boy is observed to have malformed hands, feet, and skull. Additional
examination displays jaundice, hepatomegaly, and hypotonic muscles with psychomotor
retardation. The pediatrician diagnoses the disorder as cerebrohepatorenal syndrome
(Zellweger’s syndrome). This condition is due to problems with which of the following
organelles?
a. mitochondria
b. lysosomes
c. early endosomes
d. late endosomes
e. peroxisomes
Explanation:
The answer is e. Children with cerebrohepatorenal syndrome die at an early age due to
mutations in their peroxin genes that code for defective receptors that are unable to
transfer enzymes destined for peroxisomes into these organelles. Mitochondria,
lysosomes, and endosomes are not affected by this mutation.
8. A 20-year-old male seeking help from his ophthalmologist presents with deteriorating
vision in both eyes, especially his central vision. The patient also evidences cardiac
Test Bank 4
a. lysosomes
b. early endosomes
c. late endosomes
d. mitochondria
e. peroxisomes
Explanation:
The answer is d. Leber’s hereditary optic neuropathy is due to a point mutation on the
mitochondrial DNA. Because the spermatozoon does not contribute mitochondria to the
zygote, only the female can transmit this condition to her offspring. Lysosomes,
peroxisomes, and early and late endosomes do not possess DNA.
Explanation:
The answer is b. Cadherins are integral proteins that are designed to assist cells to
maintain contact with one another. Hemidesmosomes, heparin sulfate, and basal lamina
are all associated with cell-to-extracellular matrix contact.
10. Dynein arms are always attached to one of the following. Which one is that structure?
a. central sheet
b. singlets
c. subunit A
d. subunit B
e. radial spoke
Explanation:
The answer is c. Dynein arms are microtubule-associated proteins that function in
bending of the cilium. These molecular motors are attached to the subunit A of the
axoneme. The central sheet and the radial spokes are both composed of an elastic protein
that becomes stretched during the “cocking” of the axoneme and, as they return to their
normal length, they effect ciliary motion.
Test Bank 5
11. The component of the erythrocyte cell membrane that is the most essential in
maintaining its biconcave disc shape is
a. glycophorin
b. spectrin
c. ankyrin
d. actin
e. band 3 protein
Explanation:
The answer is b. Spectrin is a rod-shaped tetramer that, in association with actin and
adducin, forms a hexagonal lattice that underlies the cytoplasmic surface of the red blood
cell plasmalemma. Ankyrin and band 3 protein and band 1 protein anchor the hexagonal
lattice to the cell membrane. Glycophorins and band 3 proteins are transmembrane
proteins.
12. A six-month-old baby boy, when seen by his pediatrician,, exhibits an enlarged
tongue and an enlarged liver. Additionally, the baby has problems with swallowing. The
pediatrician should suspect that the child is suffering from
Explanation:
The answer is b. Pompe’s disease is a lethal glycogen-storage disease that affects infants
and usually causes death by the second or third year of life. The baby is missing
lysosomal acid maltase, and as glycogen accumulates in the lysosomes of the liver, heart,
and some skeletal muscles, these organs enlarge. Although cranial nerve X distributes
through much of the body, its malfunction does not cause any of the symptoms present in
this infant. McArdle’s syndrome has an adult onset, and the symptoms of Tarui’s disease
usually are noted only after vigorous physical exercise. Tay-Sachs disease is not
accompanied by swollen tongue or enlarged liver.
13. A patient with Kartagener’s syndrome has a genetic disorder that is known to
a. affect microfilaments
b. affect intermediate filaments
c. have defective dynein
d. have defective kinesin
e. have defective -tubulin
Explanation:
Test Bank 6
14. A patient who had surgery for ovarian cancer is placed on a combination of cisplatin
and taxol therapy. Taxol is an antimitotic agent that
a. affects microfilaments
b. affects intermediate filaments
c. has defective dynein
d. prevents the polymerization of microtubules
e. stabilizes microtubules
Explanation:
The answer is e. Unlike most antimitotic agents that interfere with polymerization or
depolymerization of microtubules, taxol stabilizes microtubules, so they cannot shorten
or lengthen. In this fashion the mitotic spindle apparatus cannot change its length, thus
preventing the movement of the chromosomes during the mitotic event. Dynein,
microfilaments, and intermediate filaments are unaffected by taxol.
15. A patient with lymphoma that involves his small intestines is treated with a various
chemotherapeutic agents, including vincristine. This antimitotic substance acts on
a. -actinin
b. dynein
c. tubulin
d. myosin I
e. actin
Explanation:
The answer is c. Vincristine interferes with polymerization of microtubules and halts
mitosis, thus killing dividing cells. Vincristine has no effect on -actinin, dynein, myosin
I, or actin.
16. A two-week-old infant was seen by her pediatrician because of blistering of the
fingers and the back of her hands. The blisters were quite large and the results of the
biopsy indicated that blistering occurred in the basal layer of the epidermis. The diagnosis
was epidermolysis bullosa simplex. This disease is caused by mutations in the
a. tubulins
b. neurofilaments
c. G actins
d. keratins
Test Bank 7
e. chondroitins
Explanation:
The answer is d. Blistering in infants that occurs on the regions of the skin that are
exposed to friction and pressure is a result of mutations in types 14 and 5 keratins.
Tubulins, neurofilaments, G actins, and chondroitins are not affected.
17. Early in the morning, a male patient sees his physician because he and his wife have
been trying to start a family. According to the patient, his wife was told that she is able to
become pregnant, and he wants to have the physician check him for sterility. The
physician notices that the patient has a heavy cough. Upon questioning, the patient
reveals that he also coughs in the evening, produces a lot of sputum, and has had
numerous colds and even occasional pneumonia. The doctor asks for a sperm sample but
already is thinking of a possible diagnosis of Kartagener’s syndrome, a genetic disorder
that affects
a. a number of keratins
b. microtubule-associated proteins
c. thin filaments
d. intermediate filaments
c. thick filaments
Explanation:
The answer is b. Kartagener’s syndrome is due to an autosomal recessive disorder that
affects ciliary motion because a microtubule-associated protein, dynein, is either
defective or not present. The tubulins of microtubules are formed normally and
microtubule assembly, per se, is not affected. Thin filaments, thick filaments, and
intermediate filaments are not affected in Kartagener’s syndrome.
18. A 55-year-old patient was placed on tetracycline therapy and a week later returns to
the physician, indicating that the antibiotic did not alleviate his symptoms. During their
conversation the physician determines that the patient took the tetracycline capsules with
milk. Which of the following components of milk interfered with theaction of the drug?
a. calcium
b. lipid
c. sodium
d. rennin
e. potassium
Explanation:
The answer is a. Calcium taken within an hour of oral tetracycline ingestion interferes
with the absorption of the antibiotic through the membranes of the cells lining the
stomach and small intestines. Lipid, sodium, and potassium do not interfere with
tetracycline absorption. Rennin, an enzyme that curdles milk protein, has no effect on the
absorption of tetracycline.
Test Bank 8
19. A 77-year-old female is having problems sleeping, and her physician prescribed
flurazepam, a sleep aid. The patient reports that she feels “groggy” for about 2 days after
having taken the drug. Flurazepam is
Explanation:
The answer is d. Many drugs are inactivated by the P-450 enzyme system of the liver. In
this patient the level of this enzyme system is depressed; therefore, flurazepam is not
inactivated in 18 hours, as in most patients, but has a longer half-life, which accounts for
the groggy feeling even 2 days later. Flurazepam is not affected by HCl, pepsin, or
trypsin, nor does it enter the proteasome system of the cell.
20. In Fig. Img_001, the region at the arrow tip is the place where
Test Bank 9
Explanation:
The answer is a. The arrow tip is in the nucleolus and it is here that the assembly of both
small and large ribosomal subunits occur. rRNA, not mRNA, is transcribed in the
nucleolus, and tRNA is not degraded here. Protein synthesis as well as the coupling of
amino acids to tRNA occur in the cytoplasm, not in the nucleolus.
21. In Fig. Img_002, the collecting tubule of the kidney, water enters the lumen via
a. pinocytosis
b. endocytosis
c. aquaporins
Test Bank 10
d. ion channels
e. carrier proteins
Explanation:
The answer is c. Water leaves the cells of the collecting tubule to enter its lumen by way
of structures known as aquaporins. Pinocytosis and endocytosis both refer to substances
entering the cell. Ion channels are designed to carry ions along a concentration gradient in
or out of a cell, whereas carrier proteins can move ions as well as small molecules along
and/or against a concentration gradient.
22. In Fig. Img_004, the structure at the tip of the arrow is responsible for which of the
following?
a. synthesis of ATP
b. assembly of microtubules
c. assembly of neurofilaments
d. synthesis of lysosomal proteins
e. assembly of neurotubules
Explanation:
Test Bank 11
The answer is d. The large cell in the center of this field is a multipolar neuron in the gray
matter of the spinal cord. The arrow is pointing to a structure known as a Nissl body,
which was noted by electron microscopy to be composed of rough ER, the region where
proteins that are to be packaged, such as lysosomal proteins, are synthesized whereas
microtubules (also known as neurotubules) and neurofilaments are assembled in the
cytoplasm, but not involving the rough ER.
23. A patient who is unable to metabolize long-chain fatty acids has problems involving
her
a. early endosomes
b. late endosomes
c. lysosomes
d. peroxisomes
e. proteasomes
Explanation:
The answer is d. Peroxisomes function in the catabolism of long-chain fatty acids, in
detoxifying noxious agents, and in killing bacteria. Early and late endosomes are
organelles that participate in the endocytic and endolysosomal pathways, whereas
proteasomes function in the catabolism of proteins.
a. zonula occludens
b. zonula adherens
c. fascia occludens
d. desmosomes
e. hemidesmosomes
Explanation:
The answer is e. Integrins are transmembrane proteins that are restricted to interact with
the extracellular matrix. In epithelial cells they are localized in the basal surfaces and
assist hemidesmosomes in adhering to the basal lamina. They do not participate in cell-
to-cell contact, and all the other choices involve intracellular contact.
25. In Fig. Img_019, the core of the structures at the arrow tip is composed of
Test Bank 12
a. thin filaments
b. intermediate filaments
c. thick filaments
d. microtubules
e. actin filaments
Explanation:
The answer is d. The photomicrograph depicts a pseudostratified, ciliated columnar
epithelium and the structures at the arrow tip are cilia. The core of each cilium is consists
of an axoneme. Axonemes are composed of nine doublet microtubules surrounding two
central singlet microtubules. Thin filaments (actin filaments) constitute the core of
microvilli. Intermediate filaments and thick filaments are not associated with cilia.
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Fig. 56. Spanish Treasure-Frigate of about 1590.
One of the most memorable of naval battles was that which was
fought on the Adriatic Sea in 1571. On the one side were the allied
forces of Venice, Spain, and the Papal States: on the other, the
Turks who were defeated. Galleys and galleasses played an
important part in obtaining this victory. To what development the
galley had attained since the times of the early Greeks and Romans
will be seen in Figs. 57 and 58. But in spite of all that history had
added to them, it is surprising how little they differ in essentials. Fig.
57 has been sketched from a model in the South Kensington
Museum. It is quite old, and is said to have belonged to the Knights
of Malta. Her dimensions if built to scale would work out at about 165
feet long, by 22 feet beam, with extreme beam from gunwale to
gunwale, 31 feet. The depth would be 9·9 feet, and the number of
sweeps 44. In the United Service Museum there is also an
instructive Maltese galley model of a large size which, though of the
eighteenth century, differed so little as to be closely similar to the
excellent illustration which we give in Fig. 58. This has been taken
from an important publication, of the beginning of the seventeenth
century, by Joseph Furttenbach, entitled “Architectura Navalis,”
printed at Ulm in 1629. As will be seen, each oar is still worked by a
gang of men. At the stern the captain sits with his knights by his side,
while at the extreme stern is the pilot. Along the corsia or gangway
down the ship walk two men with long poles with which to beat the
lazy oarsmen. The principal armament was carried in the bows and
so was unable to be used for broadside fire. Notice also the survival
of the trumpeters. The length of this vessel was 169 feet from beak
to stern, with an extreme beam of about 20 feet. The word antennæ
is still found at this time as applied to the yards. In spite of the
handiness of the galley and her consequent popularity in the
Mediterranean, she was thoroughly despised by Elizabethan
seamen. Much more after their own heart was the nave or ship
shown in Fig. 59, and also taken out of Furttenbach. The reader will
notice a wise restriction of high-charged structures. This vessel, in
fact, shows a steady improvement in naval architecture. Thus,
besides the lateen mizzen she carries a square topsail above, while
in addition to the spritsail seen furled to its yard on the bowsprit,
there has now been added a sprit topsail whose yard is seen to hoist
up a sprit topmast. When we compare this vessel with the wooden
walls of the eighteenth century, she will be seen to be wonderfully
modern. The last traces of crude mediævalism are disappearing.
Science in design has fast begun to supplant rule of thumb and
guess-work based only on ignorance. Skill has taken the place of
inexperience in the work of the shipwright, and both design and
construction have been based on the knowledge obtained not only in
long and tedious voyages, but in the brisk fighting between nation
and nation and privateer against treasure ship and trader. In the
same volume of Furttenbach a useful plan of the lines of this ship is
given, from which we see that whilst the mainmast is stepped at the
keelson, the fore and mizzen are stepped on the main deck.
In 1603 James built three new ships for the Navy, and five years
later the Ark Royal of Elizabeth’s reign was rebuilt and renamed the
Anne Royal. In 1608 the keel was laid for the Prince Royal, a ship of
1200 tons, whose appearance will be found in Fig. 60. This
illustration is from a picture in the Trinity House, and is here
reproduced by kind permission of the Elder Brethren. She was the
largest and finest ship that had ever been designed for the English
Navy, and was the finest man-of-war of her time. She was both built
and designed under the supervision of Phineas Pett, Master of Arts
of Emmanuel College, Cambridge, a distinguished member of a
distinguished family which, from the reign of Henry VIII. right down to
William and Mary kept up a continuous line of naval builders and
architects. An unsuccessful attempt was made to launch her on
September 24, 1610, when it was found that the dock head at
Woolwich was too narrow to allow her to get through. She was
eventually launched successfully, however, at a later date. She was
a three-decker in the sense that she had two full batteries and an
upper deck armed. Gorgeously decorated with carvings and
paintings the Prince Royal was double-planked, and with but slight
modifications, chiefly in respect of her decoration, would not be
dissimilar to the ships built at the beginning of the nineteenth
century. Indeed so slight, comparatively, were the developments that
took place between this and the time of the Battle of Trafalgar that
the ships of the early Stuarts would not have looked out of place
among the ships of Nelson’s fleet. Between now and the close of the
eighteenth century the similarity between men-of-war and
merchantmen was so close as to make distinction practically
impossible. That, too, will account for the fact of the English in the
foregoing imaginary encounter by Smith asking whether the Spanish
vessel were a merchant or man-of-war. We have made so many
changes between the two classes of ships since then that it is a little
difficult at first to realise this.
In the design of the Prince Royal, many of the old-fashioned
conventionalities went by the board, and, as is always the case with
a daring innovation, hostile criticisms were not scarce. Some of
these, however, were justified, for when a Commission was
appointed to report on the design, it was found that more than
double the number of loads of timber were used than had been
estimated for. The Prince Royal had a figurehead representing the
King’s son on horseback, after whom she was named. Her
dimensions were: length of keel, 114 feet; beam, 44 feet. She was
pierced for 64 guns and carried 55. This number was restricted in
order to guard against the excessive top-weight. In action the vacant
portholes would be filled by guns from the opposite side of the ship.
The reader will notice how close the similarity is between the hull of
this ship and that of the merchantman in Fig. 59, of this period, taken
from Furttenbach. The disappearance of the high poop and
forecastles is particularly obvious. Three lanterns were carried at the
poop, and subsequently this vessel was cut down smaller. At the
beginning of the seventeenth century the lowest decks of ships
carried the bread and other store-rooms, the cables, the officers’
cabins as well as some of the crew. The second deck was about 6
feet above and pierced with nine ports aside.
By 1624, James’ navy contained four ships of the first rank, viz.,
the Prince Royal, the Bear, the Merhonour and the old Ark Royal,
now called the Anne Royal. Besides these there were fifteen of the
second rank, nine of the third, and four of the fourth, as well as some
hoys. It is curious to find, too, the existence still, in the navy, of four
galleys. They were a source of constant expense, being never used
now that the value of big ships had been realised, and they were
eventually ordered to be sold out of the service.
Charles I. took the liveliest interest in the Navy, and under him
naval architecture continued its progression. The first additions he
was responsible for were not of big ships, but of the sea-going
pinnesses of about 50 tons and under, equipped with both oars and
sails. They were square-rigged, three-masted, and had two decks.
They were, however, sparred and ordnanced far too heavily. In spite
of the fact that England had built a few large ships during the last
century, she had not been conspicuously active in this respect. Far
easier and cheaper had it been to capture the pick of the enemy’s
fleet, and then to refit them and turn the prizes into English men-of-
war. But this lethargy was beginning to disappear. Pett was one of
the chief influences in regard to this, and it was he who, having
closely studied the lines of a fine French ship lying in British waters,
learned some of the improvements that afterwards were embodied in
the ships of our country.
Fig. 61. The “Sovereign of the Seas.” Built in 1637.