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Metabolism in RBC &
WBC
Binaya Tamang
UCMS- Bhairahwa
Metabolism in RBC
Cytoskeletal protein: Biconcave shape?
lack of these protein; hemolytic anemia
Advantages of biconcave
• Higher ratio of surface area to volume
• To fold over and squeeze through narrow capillaries
• Minimizes distance to be traversed, efficient gas exchange
between capillary walls
• Rapidly moving Rbc( up to 2mm/s)
• Highly dependent upon glucose as its energy source.
• RBC memb. has high affinity glucose transporters.
• facilitated diffusion
• the erythrocyte is capable of glucose uptake by facilitated
diffusion b/c of
1. its low intracellular glucose concentration and
2. the presence of glucose carrier protein, or glucose
transporter GLUT;
GLUT1 in erythrocyte
Glucose, Glut in RBCs
Pathways of glucose utilization
• RBC utilize glucose via:-
» Anaerobic glycolysis
» luebering rapoport cycle
» HMP Shunt
ATP produced is utilized for
• Maintain its biconcave shape
• Transport ions ( e.g. Na/K ATPase)
• Anion exchange protein
• Water in and out of cells.
• ( overall survival of RBCs)
• Yields 2,3-BPG
• It helps in O2 unloading at tissue.
• At low pO2 at tissue, Hb has more affinity to 2,3-BPG.
• Due to ↑ concentration of 2,3-BPG in tissue, Hb binds 2,3-
BPG & leads to unloading of O2.
• Under hypoxic conditions, Anemic condition, high altitude
• To differentiate hemolytic anemia between hexokinase and
pyruvate kinase deficiency (glucose is not phosphorylated,
hence the synthesis & concentration of 2,3-BPG are low in
RBC)
Luebering Rapoport cycle in RBC
• Due to absence of mitochondria, anaerobic glycolysis occurs in
RBC.
Glucose
Anaerobic glycolysis 2 ATP
Lactate
↓
Cori’s cycle
Anaerobic glycolysis in RBC
• Yields NADPH and ribose
• What are its importance?
• G6PD deficiency anemia. Explain.
• First let us know the importance of reduced glutathione.
HMP Shunt in RBC
Imp: Generation of reduced Glutathione
• Role of GSH in RBC
– Maintains integrity of RBC membrane.
– -SH of GSH is used to reduce peroxides (ROS).
G6PD deficiency anemia
G6PD deficiency anemia: hypersensitive conditions
• X linked recessive
• Tropical Africa, Mediterranean, certain part of south asia
• Eg. Sulfanomide drugs, antimalarial primaquine, proxidant
containing food ( vicia faba)
• Exposure to chemicals like naphthalene.
• RBCs cant combact with such episodes of oxidative stress and get
lysed leading anemia.
Methemoglobin
• The ferrous iron of hemoglobin is susceptible to oxidation by
superoxide and other oxidizing agents, forming
methemoglobin, which cannot transport oxygen.
• Small quantity of methemoglobin is reduced back to the
Fe2+ state by met-hb reductase enzyme system using
NADH and cytochrome b5.
Maintenance of HB in Ferrous (Fe2+) state
• NADH prevent accumulation of Met-Hb.
• Met-Hb (Fe3+) can’t transport O2.
• 75% using NADH and cytochrome b5
• 20% is due to NADPH dependent system
• Glutathione dependent met-Hb reductase accounts for rest 5% activity.
Methemoglobinemia
Inherited : deficiency of methemoglobin reductase, AR , Hb M,
Acquired: certain drugs (eg, sulfonamides) or chemicals (eg, aniline)
Bluish coloration called cyanosis.
• Synthesis of glycogen, FA, protein, & nucleic acids doesn’t
occur in RBC.
• Some lipids (eg, cholesterol) in RBC memb. can exchange
with corresponding plasma lipids.
• During RBC degradation,
– Globin is degraded to amino acids (reutilized in body)
– Iron is released from heme & reutilized
– Tetrapyrrole of heme is converted to bilirubin,
• RBC can’t synthesize Protein
– Devoid of internal organs to deliver max of O2 to tissue
– Reticulocytes are active in protein synthesis.
– Mature RBC can’t synthesize protein.
Reticulocytes enter circulation
↓
Lose intracellular organelles within 24hr
[Ribosomes, Mitochondria]
↓
Become young RBC
↓
lose their ability to synthesize protein
BIOCHEMISTRY OF ABO BLOOD GROUP
• At least 21 human blood group systems
• ABO, Rh (Rhesus), and MN systems.
• first discovered by Landsteiner
• ABO Substances Are Glycosphingolipids & Glycoproteins
• H substance itself is formed by the action of a
fucosyltransferase, which catalyzes the addition of the
terminal fucose in α1 → 2 linkage onto the terminal Gal
residue of its precursor:
Contd….
• A substance contains an additional GalNAc
(immunodominant sugar).
• B substance an additional Gal (immunodominant sugar).
Metabolism in WBC
• Active glycolysis
• Active pentose phosphate pathway
• Moderate oxidative phosphorylation
• Rich in lysosomes (degradative enzymes)
• Contain certain unique enzymes (eg, myeloperoxidase &
NADPH-oxidase)
• Also has role in acute inflammatory response.
Metabolism in WBC
Respiratory burst of phagocytic cells
• Involves NADPH oxidase and helps kills bacteria.
• When neutrophils and other phagocytic cells engulf bacteria,
they exhibit a rapid increase in oxygen consumption known as
the respiratory burst.
Chronic granulomatous disease
Summary of important aspects of
the metabolism of the red blood cell.
Thank you

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Rbc and wbc metabolism

  • 1. Metabolism in RBC & WBC Binaya Tamang UCMS- Bhairahwa
  • 4. lack of these protein; hemolytic anemia
  • 5. Advantages of biconcave • Higher ratio of surface area to volume • To fold over and squeeze through narrow capillaries • Minimizes distance to be traversed, efficient gas exchange between capillary walls • Rapidly moving Rbc( up to 2mm/s)
  • 6. • Highly dependent upon glucose as its energy source. • RBC memb. has high affinity glucose transporters. • facilitated diffusion • the erythrocyte is capable of glucose uptake by facilitated diffusion b/c of 1. its low intracellular glucose concentration and 2. the presence of glucose carrier protein, or glucose transporter GLUT; GLUT1 in erythrocyte Glucose, Glut in RBCs
  • 7. Pathways of glucose utilization • RBC utilize glucose via:- » Anaerobic glycolysis » luebering rapoport cycle » HMP Shunt
  • 8. ATP produced is utilized for • Maintain its biconcave shape • Transport ions ( e.g. Na/K ATPase) • Anion exchange protein • Water in and out of cells. • ( overall survival of RBCs)
  • 9. • Yields 2,3-BPG • It helps in O2 unloading at tissue. • At low pO2 at tissue, Hb has more affinity to 2,3-BPG. • Due to ↑ concentration of 2,3-BPG in tissue, Hb binds 2,3- BPG & leads to unloading of O2. • Under hypoxic conditions, Anemic condition, high altitude • To differentiate hemolytic anemia between hexokinase and pyruvate kinase deficiency (glucose is not phosphorylated, hence the synthesis & concentration of 2,3-BPG are low in RBC) Luebering Rapoport cycle in RBC
  • 10.
  • 11. • Due to absence of mitochondria, anaerobic glycolysis occurs in RBC. Glucose Anaerobic glycolysis 2 ATP Lactate ↓ Cori’s cycle Anaerobic glycolysis in RBC
  • 12.
  • 13. • Yields NADPH and ribose • What are its importance? • G6PD deficiency anemia. Explain. • First let us know the importance of reduced glutathione. HMP Shunt in RBC
  • 14. Imp: Generation of reduced Glutathione • Role of GSH in RBC – Maintains integrity of RBC membrane. – -SH of GSH is used to reduce peroxides (ROS).
  • 16. G6PD deficiency anemia: hypersensitive conditions • X linked recessive • Tropical Africa, Mediterranean, certain part of south asia • Eg. Sulfanomide drugs, antimalarial primaquine, proxidant containing food ( vicia faba) • Exposure to chemicals like naphthalene. • RBCs cant combact with such episodes of oxidative stress and get lysed leading anemia.
  • 17. Methemoglobin • The ferrous iron of hemoglobin is susceptible to oxidation by superoxide and other oxidizing agents, forming methemoglobin, which cannot transport oxygen. • Small quantity of methemoglobin is reduced back to the Fe2+ state by met-hb reductase enzyme system using NADH and cytochrome b5.
  • 18. Maintenance of HB in Ferrous (Fe2+) state • NADH prevent accumulation of Met-Hb. • Met-Hb (Fe3+) can’t transport O2. • 75% using NADH and cytochrome b5 • 20% is due to NADPH dependent system • Glutathione dependent met-Hb reductase accounts for rest 5% activity. Methemoglobinemia Inherited : deficiency of methemoglobin reductase, AR , Hb M, Acquired: certain drugs (eg, sulfonamides) or chemicals (eg, aniline) Bluish coloration called cyanosis.
  • 19. • Synthesis of glycogen, FA, protein, & nucleic acids doesn’t occur in RBC. • Some lipids (eg, cholesterol) in RBC memb. can exchange with corresponding plasma lipids. • During RBC degradation, – Globin is degraded to amino acids (reutilized in body) – Iron is released from heme & reutilized – Tetrapyrrole of heme is converted to bilirubin,
  • 20. • RBC can’t synthesize Protein – Devoid of internal organs to deliver max of O2 to tissue – Reticulocytes are active in protein synthesis. – Mature RBC can’t synthesize protein. Reticulocytes enter circulation ↓ Lose intracellular organelles within 24hr [Ribosomes, Mitochondria] ↓ Become young RBC ↓ lose their ability to synthesize protein
  • 21. BIOCHEMISTRY OF ABO BLOOD GROUP • At least 21 human blood group systems • ABO, Rh (Rhesus), and MN systems. • first discovered by Landsteiner • ABO Substances Are Glycosphingolipids & Glycoproteins • H substance itself is formed by the action of a fucosyltransferase, which catalyzes the addition of the terminal fucose in α1 → 2 linkage onto the terminal Gal residue of its precursor:
  • 22. Contd…. • A substance contains an additional GalNAc (immunodominant sugar). • B substance an additional Gal (immunodominant sugar).
  • 23.
  • 25. • Active glycolysis • Active pentose phosphate pathway • Moderate oxidative phosphorylation • Rich in lysosomes (degradative enzymes) • Contain certain unique enzymes (eg, myeloperoxidase & NADPH-oxidase) • Also has role in acute inflammatory response. Metabolism in WBC
  • 26. Respiratory burst of phagocytic cells • Involves NADPH oxidase and helps kills bacteria. • When neutrophils and other phagocytic cells engulf bacteria, they exhibit a rapid increase in oxygen consumption known as the respiratory burst.
  • 27.
  • 28.
  • 30. Summary of important aspects of the metabolism of the red blood cell.