blood and hematopoietic tissue Flashcards

1
Q

functions of blood

A
  1. deliver of nutrients and O2 directly or indirectly to cells
    2.transport of wastes and CO2 away from cells
  2. delivery of hormones and other regulatory substances to and form cells and tissues
  3. maintenance of homeostasis
    - by acting as a buffer
    - participating in coagulation n thermoregulation
  4. transport of humoral agents n cells of the immune systems that protect body from pathogenic agent, foreign proteins & transformed cells (cancer cells)
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2
Q

it is used to measure hematocrit levels in blood samples

A

microhematocrit tube
[Measurement Scale: Percentage scale (0-100) to assess blood component proportions.
Sealant: Closes the tube to prevent sample leakage.]

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3
Q

characteristics of erythrocytes

A

anucleate - no nucleus and organelles
biconcave, discoid - for deformability, to be highly flexible and pass in narrow (capillaries)
lifespan: 120 days

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4
Q

diameter of erythrocytes

A

7-9um, larger than pericytes
[pericytes are support cells that wrap arnd capillaries]
*smaller RBCs may indicate anemia

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5
Q

the major reddish protein which binds O2 and transports CO2 throughout the body

A

hemoglobin
- changes can be seen in structure

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6
Q

unction of the splenic filter

A

checks RBCs in the spleen and removes old or damaged ones through phagocytosis
when it successfully passes the splenic filter = “Badge of Success” which can be located in the Central Pallor of the RBCs

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7
Q

What happens to RBCs after 120 days

A

become senescent
lose membrane integrity due to a lack of energy
= phagocytized by the splenic filter

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8
Q

what structural feature of the RBC membrane enables its flexibility?

A

the lipid bilayer

the main components/ RBC membrane lipids:
- cholesterol
-phospholipids
- glycolipids

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9
Q

the 2 phospholipids found in the
- outer layer
- inner layer
- both
of the RBC membrane lipids

A

OUTER
■ Phosphatidylcholine
■ Sphingomyelin

INNER
■ Phosphatidylethanolamine
■ Phosphatidylserine
- serve as marker for Senescent RBCs

BOTH
■ Phosphatidylinositol
■ Cholesterol

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10
Q

the 5th phosolipid

A

phosphatidylinositol (PI)

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11
Q

process of RBC removal

A

Healthy RBCs
→ Have Phosphatidylserine (PS) inside the membrane (hidden).

Aging RBCs (Senescent RBCs)
→ After 120 days, the RBC loses energy and its membrane weakens.

Flipping Signal
→ Phosphatidylserine (PS) flips to the outer surface of the membrane.

Macrophage Detection
→ Splenic macrophages (immune cells in the spleen) recognize the flipped PS as a signal that the RBC is old and needs to be removed.

Phagocytosis (RBC Removal)
→ The spleen’s macrophages engulf and digest the old RBC.

End Result
→ The body recycles useful parts of the RBC (like iron from hemoglobin) and removes waste.

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12
Q

what is attached to glycolipids in the RBC membrane and its function

A

Glycosylphosphatidylinositol (GPI)-linked protein (GPI-linked proteins)
- can protect RBC from immune system

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13
Q

What happens when GPI is defective or missing?

A

RBC lose protection = vulnerable to immune system destructin (hemolysis)

Paroxysmal Nocturnal Hemoglobinuria
- causes RBC breakdown, leading to anemia and dark anemia
- happens mostly at night as body’s pH drop during sleep = triggers immune attack on unprotected RBCs

1️⃣ Paroxysmal – Sudden episodes of fever/chills.
2️⃣ Nocturnal – Happens at night.
3️⃣ Hemoglobinuria – Dark-colored morning urine due to hemoglobin release.

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14
Q

is PNH an autoimmune disease

A

not exactly - immune system attacks RBC by mistake as they lack protection not because it is directly targeting them

hence leading to random hemolysis

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15
Q

The presence of free hemoglobin in urine due to RBC destruction (hemolysis).

A

hemoglobinuria

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16
Q

what is attached to the Glycosylphosphatidylinositol

A

carbohydrate chains
- acts as an “anchor” for certain extracellular membrane proteins on the RBC surface
- protect from immune system attack

[lipid tail that embeds into the RBC membrane.
has a carbohydrate (sugar) chain that helps attach protective proteins
prevent the immune system from destroying RBCs]

GPI = “Glue” that holds protective proteins on RBCs

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17
Q

what is the arrangement of molecules in the RBC membrane

A

interspersed
- diff types of lipids and cholesterol are scatted throughout the bilayer

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18
Q

two main types of RBC membrane proteins

A

Transmembrane Proteins:
- aka integral proteins
- directly bound to the cell membrane
- approx. 300 found in the RBCs
- can be receptors/ channels/ transporters

Cytoskeletal Proteins:
- maintains overall shape

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19
Q

briefly explain the transmembrane function and their functions

A

Band 3 Protein:
most common
serve as
- anion exchange transporter
- assembly site for ABO blood group system antigen
[ABO blood group recognition.]

Glycophorins (A, B, C):
common
serve as cyanic acid transporter

Glut-1:
glucose transporter [help absorb glucose for energy]
serve as assembly site for ABO blood group system antigen

Kell, Kidd, Duffy, RhAG, Rh:
serve as their own blood group system

*Band 3 Protein and Glut-1 serve as assembly sites for ABO antigens

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20
Q

Glycophorins (A, B, C) blood group identifications

A

A → Related to the MN blood group system.
[Decides if you have M or N blood type.]

B → Related to the S blood group system.
[Helps determine if you have S blood type.]

C → Related to the Gerbich blood group system.
[Connected to the Gerbich blood group.]

[found on the surface of RBC which help interact w their environment and carry blood group markers

like ID tags on your RBCs, helping doctors match the right blood during transfusions]

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21
Q

why are blood group proteins important

A

identify blood types to avoid mismatched transfusions.
help in transporting important molecules.
duffy helps protect against malaria infection by stopping the parasite from entering RBCs.

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22
Q

Kell →
Kidd →
Duffy →
RhAG and Rh →

A

Kell → zinc-binding endopeptidase
[Uses zinc to help RBCs function properly.]

Kidd → urea transporter
[Moves waste out of RBCs.]

Duffy → G-protein coupled and chemokine receptors, malarial parasite
[Helps immune signals and protects against malaria.]

RhAG & Rh → Mitigating/ decreasing transfusion reaction
[Help prevent bad reactions during blood transfusions.]

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23
Q

briefly explain the cytoskeletal protein and their functions

A

Spectrin (α-Spectrin & β-Spectrin):
- major filamentous proteins that maintain shape
[flexible network inside RBC = can bend w/o breaking ]

Ankyrin:
- anchors for diff transmembrane/ cytoskeletal proteins
- when group tgt = ankyrin complex which maintains vertical structure of the RBC membrane
[glue that holds transmembrane an cytoskeletal proteins tgt]

Protein 4.1:
- same function w ankyrin
- binds other protein
- Protein 4.1/Actin Junctional Complex
[works w actin in the protein 4.1/Actin Junctional Complex to support the RBC shape]

*major is the Spectrin while the othersare Ankyrin and Protein 4.1

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24
Q

what happens when the ankyrin in the cytoskeletal membrane are grouped tgt

A

it forms an ankyrin complex
- maintains vertical structure of the RBC membrane
[glue that holds transmembrane an cytoskeletal proteins tgt]

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25
these are carbohydrate chain that has a specific sequence
antigens - molecules/ proteins that react with the antibody
26
briefly explain the following - Type 2 precursor chain - "H" antigen - "A" antigen - "B" antigen
(refer to image for diagram) Type 2 precursor chain: must assemble first to form ABO chain "H" antigen: contains a blood type already 3 stages: - Stay as “H” antigen = blood type O - Converts to A-antigen = blood type A - Converts to B-antigen = blood type B (blood type AB: has A and B antigen) "A" antigen: "B" antigen:
27
antigens and antibodies found in each blood-type (A, B, AB, O)
type A: antigens - A & H antibodies - B type B: antigens - B & H antibodies - A type AB: antigens - A, B & H antibodies - nil type O: antigens - H antibodies - B & A
28
why is type O consideres the universal dono
as it lacks A and B antigens on the surface of RBC
29
it is the universal recipient
type AB blood - often called "royal blood" - as it has both A and B antigens but no anti-a or anti-B antibodies in the plasma
30
universal donor vs universal recipient
Universal donor (Type O, especially O negative) → Can give blood to anyone because it has no antigens that could cause a reaction. Universal recipient (Type AB, especially AB positive) → Can receive blood from anyone because it has no antibodies to attack donor blood.
31
what happens if there is no H antigens
Bombay Phenotype (rare blood type) - does not have H antigen (which is needed to form A or B antigens) - first discovered in India - they appear as type O but cannot receive regular O blood
32
What happens if an Rh-negative mother is pregnant with an Rh-positive baby?
mother's immune system may see the baby's Rh protein as a threat and attack it. = Hemolytic Disease of the Newborn (HDFN)?
33
A condition where the baby’s red blood cells are destroyed due to the mother’s immune response against Rh-positive cells.
Hemolytic Disease of the Newborn (HDFN) - usually happens in the second pregnancy - example: Mother is Rh (-), Baby is Rh (+) since they have different blood types, higher chance that mom attacks the fetus due to hemolysis of RBC
34
briefly explain the Rh incompatibility in the first and second pregnancy
first pregnancy: not a problem - mother's immune system is exposed to Rh-positive cells for the first time and does not have a strong reaction yet second pregnancy: dangerous - mother’s immune system "recognized" the Rh protein and attacks the baby’s red blood cells
35
If someone is O+ but has no Rh protein, are they really O−?
Rh factor is determined by the presence of the Rh protein. If they truly have no Rh protein, they would be classified as Rh-negative (O−), but there may be genetic variations.
36
it serves as ammonia transported found in the blood group antigens
RhAG Rh-associated glycoproteins
37
This protein is embedded in the red blood cell membrane that helps transport ammonia and supports the structure of Ph proteins
RhAG (Rh-associated glycoprotein)
38
These proteins determine a person's Rh blood type (positive or negative).
RhCE and RhD Proteins - different variation of these proteins affect blood compatibility in transfusions *RhD is clincally ignificant in preggy mum
39
what are the clinical correlation in RBC (blood disorders)
(refer to ppt) spherocyte: - round, no central pale area - less flexible, breaks easily - seen in hereditary spherocytosis, autoimmune hemolysis ellipocyte/ ovalocyte: - oval or elongated - less flexible but still moves through vessels - seen in hereditary elliptocytosis, iron deficiency anemia
40
what is hemoglobin composed of
a large protein made up of 4 subunits 2 types of globin chains - 2 alpha - 2 non-alpha which can be β (beta), γ (gamma), or δ (delta), depending on the hemoglobin type = these 4 chains are folded and connected tgt
41
briefly explain the types of hemoglobin
composed of 4subunits: 1. HbA (Adult Hgb) most common type in adults major hemoglobin in the body made of 2 alpha and 2 beta chains 2. HbA2 (less than HbA) made of 2 alpha and 2 delta chains 3. HbF (Fetal Hgb) found during newborn and at birth made of 2 alpha and 2 gamma chains it holds onto oxygen better than adult hemoglobin to help the baby get oxygen from the mother 4. HbA1C reflects glucose concentration in blood for the past 2-4 months - high HbA1C may indicate diabetes
42
main components of heme
1. Protoporphyrin IX (PPIX) ring ■ Fe2+: binds to the O2 molecule 2. Ferrous Iron (Fe²⁺) ■ RBC with ferric ion = carboxyhemoglobin [ Fe²⁺ is converted to Fe³⁺ = forms carboxyhemoglobin, which cannot bind oxygen properly]
43
How many heme groups are in one hemoglobin molecule?
4 heme groups, one in each subunit 4 oxygen molecules is carries in 1 Hgb (since each heme group binds to one oxygen)
44
briefly explain the 2 states of the Hemoglobins
1. Tense ("T") State no proportion/ conformation of protein no O2 found, only 2,3-BPG (Bisphosphoglycerate) 2. Relaxed ("R") State once O2 binds to heme, have movement/ change in the conformation a-subunit and another β-subunit rotate 15 degree from its normal conformation
45
briefly explain how the CO2 transport in the tissue (venous blood - deoxygenated blood) and CO2 release in the lungs (arterial blood - oxygenated blood)
CO₂ Transport in the Tissues (Venous Blood – Deoxygenated Blood): 1. CO₂ Enters RBCs → CO₂ from tissues enters the RBC 2. Carbonic Acid Formation → Inside the RBC, CO₂ combines with H₂O to form carbonic acid (H₂CO₃) → Sped up by an enzyme called carbonic anhydrase 3. Breakdown of Carbonic Acid → Carbonic acid quickly splits into: Bicarbonate (HCO₃⁻) (which is sent out of the RBC) Hydrogen ion (H⁺) (which stays inside the RBC) 4. Chloride Shift → To keep the electrical balance, a chloride ion (Cl⁻) enters the RBC as bicarbonate leaves 5. Oxygen Release → The H⁺ binds to hemoglobin, causing it to release oxygen into the tissues 6. Deoxygenated Hemoglobin → Hemoglobin now carries CO₂ instead of oxygen CO₂ Release in the Lungs (Arterial Blood – Oxygenated Blood): 1. Oxygen Enters RBCs → Oxygen from the lungs binds to hemoglobin, forcing H⁺ to be released. 2. CO₂ Formation → The free H⁺ combines with bicarbonate (HCO₃⁻) inside the RBC to form carbonic acid (H₂CO₃). 3. Carbonic Acid Breakdown → Carbonic acid splits back into CO₂ and water (H₂O). 4. Reverse Chloride Shift → Bicarbonate enters the RBC, while chloride exits to maintain balance. 5. CO₂ Expelled → The newly formed CO₂ diffuses out of the RBC and is exhaled through the lungs. [In tissues, CO₂ enters RBCs, turns into carbonic acid, releases H⁺, and helps unload oxygen. In the lungs, oxygen binds to hemoglobin, which forces H⁺ to recombine with bicarbonate, creating CO₂ that is exhaled. The chloride shift helps maintain balance in RBCs.]
45
briefly explain curve A,B and C in the Hemoglobin-Oxygen Dissociation Curve
(transes) curve A: hemoglobin tends to bind O2 more tightly than normal ● Increased pH, decreased H ions ● Decreased pCO2 ● Decreased 2,3-DPG ● Decreased temperature curve B: pH (H⁺): Normal arnd 7.35-7.45 pCO₂ (partial pressure of CO₂): Normal (35-45 mmHg) 2,3-DPG (Diphosphoglycerate): Normal lvls Temperature: Normal, 37°C curve C: results in release of O2 and decreased affinity of hemoglobin to O2 ● Decreased pH, Increased H ions ● Increased pCO2 (partial pressure) ● Increased 2,3-DPG ● Increased temperature
46
explains what events/ environmental status is needed to release or bind oxygen
Hemoglobin-Oxygen Dissociation Curve
47
it is the last immature RBC stage
reticulocytes/ retics - usually in small amounts
48
how long does the reticulocytes lases in the - bone marrow - peripheral blood
stay in the BM for abt 2 days then enter the blood stream for 1 day or more before fully maturing into RBC
49
Reticulocytes vs. Normal Mature Erythrocytes
Reticulocytes: - are immature - contains cytoplasmic remnants (mitochondria, endoplasmic reticulum, nucleus) - larger than rbc Erythrocytes: - no cytoplasmic inclusions
50
what happens if there is increased amt of reticulocytes
one can have anemia - the bone marrow compensates w the decrease mature RBCs by releasing more immature RBCs in the peripheral blood
51
what type of stain is used to identify the reticulocytes
Methylene Blue Stain - to see all the cell parts inside reticulocytes - stains cytoplasmic remnants, revealing identity
52
functions of hemoglobin
○ O2 Transport ○ CO2 Transport
53
it is a loosely related category of cell types dedicated to protecting their host from infection and injury
Leukocytes or White Blood Cells (WBCs)
54
briefly explain the 2 parts of immune system
1. Innate Immune System [first line of defense] - majority of leukocytes - immune system that does not specify which foreign material is attacked, non-specific response 2. Adaptive Immune System [second line of defense] - largely performed by the lymphocytes - response is highly specific - it memorize the foreign material [response is faster and stronger] - once the 2nd attack happens, it will hv a heightened response
55
briefly explain the 2 categories of leukocytes
1. granulocytes - contains cytoplasmic granules that are evident in the peripheral blood smear a. neutrophils - polymorphonuclear neutrophil (PMN) [having a nucleus with multiple shapes (lobes) PMN and Neutrophils are the same thing—PMN is just a scientific term] - increase = bacterial infection - neutrophil band immature neutrophils signify bacterial infection b. eosinophils - contains 2 lobes - stained is orange/slightly-pinker then neutrophils - increase = parasitic infections or allergic reactions c. basophils - rare granulocytes - not normally seen in peripheral blood blood smear - stain is darer compared to other WBC - increases = allergic reactions 2. mononuclear cells a. monocytes - macrophage that travels in the peripheral blood - from blood to tissues = matures to macrophages - phagocytic cells, larger cells often in a peripheral blood smear b. lymphocytes - involves in adaptive immunity - approx size of and RBC - thin rim of cytoplasm - majority of the portion ins covered by nucleus
56
scientific term of neutrophils
Polymorphonuclear Neutrophil (PMN)
57
Immature neutrophils that appear when your body is fighting a severe bacterial infection
Neutrophil Bands
58
what are the 2 types of lymphocytes
B-Lymphocytes [make antibodies] T-Lymphocytes [directly attack infected or cancerous cells]
59
they are part of the immune system that phagocytize and destroy foreign material and microorganisms
neutrophils classification of granules: - pri granules - sec granules - tertiary granules - secretory granules
60
Process of travelling/migration of neutrophils in response to signaling proteins (Chemokines)
Chemotaxis [body release chemokines to call neutrophils. once detected, it moves toward the site of innfection] two types: ○ Intravascular Chemotaxis - occurs in the BV ○ Extravascular Chemotaxis
61
briefly explain Intravascular Chemotaxis and Extravascular Chemotaxis
Intravascular Chemotaxis: 1. Tethering and Rolling - Integrine receptors in N will come out of the surface and this protein will transiently bind to the selectins of epithelium - In response to further stimulation by chemokines, it will release/ provide more integrins in the surface [N slow down in the blood integrins on the N surface stick lightly to selectins on BV walls. N "rolls" along the BV wall, looking for an exit.] 2. Adhesion - When more integrins are present, it will bind with ICAM-1, an adhesion molecules found in epithelium [stronger infection signal (chemokines), they produce more integrins.] - It will tightly bind to integrins of the N, where it will stay 3. Crawling - Endothelium will provide a way for N to migrate out of the BV - N will extend its pseudopods on the tight junctions of endothelium - Communication between integrins and selectins will permit the N to move through tight junctions 4. Diapedesis - Once it migrates out of tight junctions, it can migrate out of the BV - It will then migrate to the tissues towards the site of infection Extravascular Chemotaxis: - once at the site of tissue injury , the neutrophil must first recognize any foreign substances before phagocytosis can occur - N have variety of receptors on their cell membranes that recognize and bind to bacteria, foreign organisms and other infectious agents ✔ Fc receptors ✔ Complement receptors ✔ Toll-like receptors
62
briefly explain the different type of receptors that neutrophils have
Fc receptors: antibody recognizing receptors recognize microorganisms that are covered by antibodies Complement receptors: recognize complement proteins - increase during inflammation covers an antigen = N can recognize Toll-like receptors: found in phagocytic cells highly specific towards certain microorganism recently discovered as part of the adaptive immunity
63
what happens during phagocytosis in neutrophils
1. Starts with the Recognition of the foreign material which is facilitated by surface receptors 2. Once it recognizes, it will form pseudopods, extending and covering the whole foreign material 3. Once it is covered completely, it will engulf the foreign material using phagosome - Vesicle inside the neutrophil containing foreign material 4. Phagosome will combine w Lysosome to form Phagolysosome = release content to bacteria 5. Result to the digestion of the material and the exocytosis of the foreign material
64
what happens to glucose and oxygen levels in a neutrophil during phagocytosis
increase noticeably, a process called respiratory burst.
65
A metabolic process where glucose and oxygen usage spikes, leading to the production of reactive oxygen species (ROS).
respiratory burst in neutrophils - important as it produces ROS, reactive oxygen species, which kills and degrades bacteria
66
Highly reactive molecules produced during respiratory burst that help digest and destroy foreign materials
reactive oxygen species (ROS) - after N engulfs a pathogen, it increase O2 consumption, triggering respiratory burst = generates ROS to destroy pathogen
67
briefly explain the Neutrophil killing mechanism
1. Respiratory Burst & Reactive Oxygen Species (ROS) 2. Myeloperoxidase System (MPO System) - Azurophilic (Pri) Granules taht contains enzyme Myeloperoxidase (MPO) will catalyze the formation od Hypochlorous Acid from H ions, Cl ions, and Hydrogen Peroxide inside the phagosome, which can easily degrade the foreign material 3. Phagocyte Oxidase System - increased O2 and glucose utilization in WBC - glucose inside N will stimulate the pentose phosphate pathway, which helps degrade glucose - NADPH (byproduct) is detected by the enzyme NAPDHH oxidase which will then stimulate the prodution of rective O2 species that can form other species
68
what is an alternative route of bacterial killing performed by neutrophil
NETosis - unique neutrophil cell death that results to the release of neutrophil extracellular (NETs) ○ Once the neutrophil finishes it job, it will release all of its contents to the extracellular fluid ○ Histones/Nucleosomes inside the neutrophils are unwound to form the actual length of Neutrophil DNA, resulting to a net-like appendix that contains the original granules ○ This net/granules catches/traps the other foreign materials that was not phagocytosed, degraded using the granules that are also bound to the net [cell releases a web-like DNA net (NET) coated with toxic granules to trap and kill bacteria. This ensures that even after the neutrophil dies, it continues fighting infection. However, excessive NETs can lead to inflammation and autoimmune diseases.]
69
a small, membrane-bound, anucleate cytoplasmic fragments derive from megakaryocytes
thrombocytes - can be divided into 4 zone base on organization and function ○ Peripheral zone ○ Structural zone ○ Organelle zone ○ Membrane system
70
briefly explain the 4 zone of the platelets
○ Peripheral zone Outermost portion Contains glycocalyx and membrane ○ Structural zone Contains microtubules, actin, and myosin Maintains the shape of the platelets ○ Organelle zone Somehow still contains small organelles inside its body (mitochondrion, glycogen, granules that contain proteins involved in coagulation, and some lysosomes) ○ Membrane system A series of open system inside platelets Surface-Connected Canalicular System ● Where calcium is usually bound ● In cases of normal platelets, it has a shape of concave/biconcave; however, in cases of activation, its surface forms pseudopods which will try to bind together to other platelets or other tissues ■ Dense Tubular System
71
what does the peripheral zone and strucural zone of platelets contain
○ Peripheral zone glycocalyx and membrane ○ Structural zone microtubules, actin, and myosin - maintains the shape
72
how does the membrane system in platelets helpthem function properly
Surface-Connected Canalicular System – Acts like channels inside the platelet, storing calcium, which is important for clotting. - When platelets are inactive, they are disc-shaped, but when activated, they form extensions (pseudopods) to stick to other platelets and tissues. Dense Tubular System – Stores calcium and other molecules needed for platelet activation and blood clotting.
73
what are the process of hemostasis in thrombocytes
3 stages: ○ Primary hemostasis vasoconstriction platelet activation primary product if for platelet plug ○ Secondary hemostasis coagulation system is activated final product is the fibrin clot ○ Fibrinolysis degradation of fibrin clot
74
where does the hematopoietic tissue located
Bone marrow - For adult age, it is usually restricted here Lymph nodes Spleen Liver Thymus
75
One of the largest organs in the body, is located within the cavities of the cortical bones
bone marrow
76
yellow vs red bone marrow
○ Yellow Marrow Contains adipose tissues ○ Red Marrow Sites of active production of RBC & WBCs In adults, restricted to: ● Sternum ● Vertebrae ● Scapulae ● Pelvis ● Ribs ● Skull ● Proximal portion of long bones
77
what can be found in the bone marrow
Hematopoietic Cord which contains - hematopoietic microenvironment that is essential and beneficial to the maturity of the RBCs and WBCs - numerous immature blood cells
78
how do we obtain a sample from the bone marrow
done through bone marrow biopsy process collected in the lliac crest (pelvis)