1In the mesoblastic stage of fetal development, blood cells are made in
In the mesoblastic stage of fetal development, blood cells are made in yolk sac
2A little later in development, blood comes from , , and
A little later in development, blood comes from liver, spleen, and lymph nodes
3Very late in fetal development, blood is from and
Very late in fetal development, blood is from bone marrow and lymph node
4Erythropoietin is made in the
Erythropoietin is made in the kidneys
5 is the last stage with the nucleus. Our mature red blood cells lack and
Orthochromatic normoblast is the last stage with the nucleus. Our mature red blood cells lack organelles and nuclei
6Unlike typical red blood cells, reticulocytes are able to make
Unlike typical red blood cells, reticulocytes are able to make hemoglobin
7Orthochromatic erythroblasts become and they become
Orthochromatic erythroblasts become reticulocytes and they become eyrthrocyte
8What are 3 things that cause erythropotein release?
1. Anemia
2. High elevation
3. Increased metabolic demand
9 stimulates enhanced erythropoisesis in bone marrow
Erythropotein stimulates enhanced erythropoisesis in bone marrow
10Red blood cells have a that allows for maximal /
Red blood cells have a biconcave disk that allows for maximal surface/volume
11Normal red blood cell death occurs after 120 days due to loss of membrane , , and
Normal red blood cell death occurs after 120 days due to loss of membrane flexibility, oxidation, and damage during circulation
12Abnormal RBC lifespan = , ,
Abnormal RBC lifespan = defective membrane (atypical hemoglobin), enzyme deficiency, infection
13Red blood cells are predominatly made of , then , then
Red blood cells are predominatly made of protein, then lipids, then carbohydrates
14Blood groups are attached to
Blood groups are attached to glycophorin
15Majority of protein in RBC is
Majority of protein in RBC is hemoglobin
16The enzymes in hemoglobin include those for , , ,
The enzymes in hemoglobin include those for glycolysis, PPP, Co2 hydration/dehydration, reduction with glutathione
17Glutathione (*γ glutamylcysteinylglycine) has a cysteinyl group that increases levels of in the process of . You don't want (in your hemoglobin) because it cannot bind oxygen and glutathione allows for its reduction.
Glutathione (*γ glutamylcysteinylglycine) has a cysteinyl -SH group that increases levels of reduced glutathione (GSSGR) in the process of aerobic glycolysis. You don't want FE3+ (in your hemoglobin) because it cannot bind oxygen and glutathione allows for its reduction.
18If hemoglobin goes from F2+ to F3+, it can
If hemoglobin goes from F2+ to F3+, it can no longer bind O2
19Enzymes in the cytoplasm of RBC are for
Enzymes in the cytoplasm of RBC are for antioxidant activity
20The 5 enzymes for antioxidant activity
1.
2.
3.
4.
5.
The 5 enzymes for antioxidant activity
1. superoxide dismutase
(O2-)
2. glutathione (GSH) peroxidase
(lipid- and hydrogen- peroxides)
3. glutathione reductase
(restores GSH)
4. catalase
(H2O2)
5. glucose
6-phosphate dh
(NADPH)
21Gluathione peroxidases detox and by .
Gluathione peroxidases detox H2O2 and lipid peroxides by reduced glutathione.
22Glutathione reductase restores
Glutathione reductase restores glutathione Peroxidase
23Glutathione Peroxidase
+
(or lipid peroxide)
→ +
(or lipid hydroxide)
Glutathione Peroxidase
2 GSH + H2O2
(or lipid peroxide)
→ GS-SG+ 2H2O
(or lipid hydroxide)
24Glutathione Reductase
+ + →
+
Glutathione Reductase
GS-SG + NADPH + H+ →
2GSH + NADP+
25 + to
+
methemoglobin reductase
Hb(Fe3+)+ NADH to
Hb(Fe2+) + NAD+
methemoglobin reductase
26The n-terminal region of the cytoplasmic domain of band 3 binds , , , and .
The c-terminal of the band 3 binds .
The n-terminal region of the cytoplasmic domain of band 3 binds deoxy hemogloobin, hemichromes, G3P, and aldolase.
The c-terminal of the band 3 binds carbonic anhydrase II.
27Deoxyhemoglobin is more prevelant in the
Deoxyhemoglobin is more prevelant in the peripheral tissues
28 High oxygen causes enzymes to bind to band 3, which halts , , and and favors
High oxygen causes enzymes to bind to band 3, which halts glycotic pathway, ATP, and NADH and favors PPP (production of NADPH)
29Low oxygen causes enzymes to unbind from , which activates the glycolytic pathway that produces and and downregulates
Low oxygen causes enzymes to unbind from band 3, which activates the glycolytic pathway that produces ATP and NADH and downregulates PPP (NADPH production)
30Red Cell Metabolism is Balanced
(by binding to )
to Optimize the Availability of
when [Oxygen] is High
…and
production when [
is lower.
Red Cell Metabolism is Balanced
(by deoxy Hb binding to Band 3)
to Optimize the Availability of
NADPH when [Oxygen] is High
…and maximize ATP
production when [O2]
is lower.
31The conformational change to
also triggers the
from the
erythrocyte.
ATP is a
The conformational change to
deoxy Hb also triggers the
release of ATP from the
erythrocyte.
ATP is a vasodilator.
32The erythrocyte “makes a path”
for itself by as
it encounters low
The erythrocyte “makes a path”
for itself by dilating vessels as
it encounters low [O2]
33These results suggest that the addition of
to the treatment regimen for
could have beneficial effects on
tissue oxygenation,
which would help to ameliorate the
concomitant
peripheral vascular disease.
These results suggest that the addition of C-peptide
to the treatment regimen for
type 2 diabetes
could have beneficial effects on
tissue oxygenation,
which would help to ameliorate the
concomitant
peripheral vascular disease.
34 binds in low oxygen concentration (using to form)
2,3 BPG binds in low oxygen concentration (using mutase to form)
352,3 BPG is made from (from glycolysis)
2,3 BPG is made from 1,3 BPG (from glycolysis)
36No matter of blood type, you have an .
No matter of blood type, you have an H antigen.
37A antigen has fucose, and N-acetylgalactosamine, and galactose
A antigen has 1 fucose, and 2 N-acetylgalactosamine, and 1 galactose
38B antigen has galatcose, fucose, and n-acetylgalactosamine
B antigen has 2 galatcose, 1 fucose, and 1 n-acetylgalactosamine
39In o blood type, there is n-acetylgalactosamine, galactose, and fucose
In o blood type, there is 1 n-acetylgalactosamine, 1 galactose, and 1 fucose
40In bombay's phenotype, there is no . There is just galactose and n-acetylgalactosamine
In bombay's phenotype, there is no H antigen . There is just one galactose and one n-acetylgalactosamine
41Megaloblastic (Macrocytic)
Megaloblastic (Macrocytic)
95-150 fl
42Microcytic
Microcytic
<83 fl
43Normocytic
Normocytic
approx 90 fl
44In nonhemolytic anemia, reticulocyte is or
In nonhemolytic anemia, reticulocyte is
normal or
low. 
45In hemolytic anemia, there are both and causes. Recticulocyte count is
In hemolytic anemia, there are both
intrinstic and
extrincic causes. Recticulocyte count is
elevated. 
46Causes of marcocytic anemia can be and
Causes of marcocytic anemia can be
megaloblastic and
non-megaloblastic 
47Causes of microcytic anemia can be rembered by the acronym
Causes of microcytic anemia can be rembered by the acronym
SALTI 
48Polycythemia vera = making of blood cells, but is
Polycythemia vera = making alot of blood cells, but erythropoietin is not elevated
49Physiological polycythemia = making of blood cells, but is
Physiological polycythemia = making a lot of blood cells, but erythropotein is elevated
50Dehydration causes
Dehydration causes polycythemia
51In hemolytic anemia, these two enzymes are deficient
1.
2.
In hemolytic anemia, these two enzymes are deficient
1. Glucose 6-Phosphate dehydrogenase
2. Pyruvate kinase
52In space, erythropoises was but was
In space, erythropoises was reduced but was reversible.
53High partial pressure of oxygen leads to high
High partial pressure of oxygen leads to high hemoglobin saturation
54Emden Meyerhof pathway EMP =
Emden Meyerhof pathway EMP = glycolosis
55In sickle hemoglobin, problem with pathway. Sickle cell of hemoglobin "pretends" to be deoxy and shunts path towards instead of .
In sickle hemoglobin, problem with pathway. Sickle cell of hemoglobin "pretends" to be deoxy and shunts path towards PPP instead of glyolysis.
56For megaloblastic, is mostly problems with . The DNA growing slowly, but keeps growing = cell.
For megaloblastic, is mostly problems with DNA production. The DNA growing slowly, but cytoplasms keeps growing =larger cell.
57 Example of physiological polycythemia=
Example of physiological polycythemia= difference in elevation