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90 Cards in this Set
- Front
- Back
erythropoiesis is making ___
myelopoiesis is making ___ (2) thrombopoiesis is making ___ |
RBCs
granulocytes monocytes platelets |
|
automatic counters use ___ for differential white cell counts
|
cellular peroxidase
|
|
macrocytosis is caused by (2)
|
liver disease
alcoholism |
|
target cells are caused by (4)
|
Fe deficiency
liver disease Hbopathy splenectomy |
|
stomatocytes are caused by (2)
|
liver disease
alcoholism |
|
pencil cells are caused by
|
Fe deficiency
|
|
echinocytes are caused by (2)
|
liver disease
splenectomy |
|
acanthocytes are caused by (3)
|
liver disease
abetalipoproteinemia renal failure |
|
microspherocytes are caused by (3)
|
hereditary spherocytosis
AIHA septicemia |
|
fragments are caused by (4)
|
DIC
HUS TTP cardiac valve problems |
|
elliptocytes are caused by
|
hereditary elliptocytosis
|
|
tear drops are caused by
|
myelofibrosis
|
|
basket cells are caused by
|
oxidative damage, e.g. G6PD deficiency
|
|
microcytes are caused by (2)
|
Fe deficiency
thalassemia |
|
mean life span of RBC
|
120 days
|
|
mean life span of platelet
|
8--10 days
|
|
mean life span of neutrophil
|
2--4 days
|
|
mean life span of monocyte
|
months
|
|
mean life span of lymphocyte
|
months
|
|
hemopoiesis during the first 6 weeks of gestation is in the ___
|
yolk sac
|
|
hemopoiesis from week 6 till month 6-7 is in the ___ (2)
|
liver
spleen |
|
hemopoiesis from month 6-7 and on is in the ___
|
BM
|
|
at birth all BM is ___ aka ___. in adults it's found in ___. (2)
|
hematopoietic
red axial skeleton proximal long bones |
|
2 ways to examine BM are ___.
|
aspiration
biopsy |
|
aspiration is commonly done from ___
biopsy is commonly done from ___ |
sternum
iliac crest |
|
steps in normoblastic erythropoiesis (5)
|
proerythroblast
basophilic erythroblast polychromatic erythroblast pyknotic erythroblast erythrocyte |
|
if RNA is present in an erythroblast it's called a ___
|
reticulocyte
|
|
a small peripheral nucleus is called a ____
|
Howell-Jolly body
|
|
process of granulocyte production is called ___
|
myelopoiesis
|
|
steps in myelopoiesis (6)
|
myeloblast
promyelocyte myelocyte metamyelocyte stab polymorph |
|
___s have primary granules
|
promyelocyte
|
|
___s have secondary granules
|
myelocyte
|
|
___ granules are present in all granulocytes
|
primary
|
|
___s are the first myeloid stage with no nucleolus
|
myelocyte
|
|
nucleus begins to indent at the ___ stage
|
metamyelocyte
|
|
because of ___ acute promyelocytic leukemia is more dangerous than acute myeloblastic leukemia
|
granules can cause DIC
|
|
the first stage in myelopoiesis after mitosis has stopped is ___
|
metamyelocyte
|
|
to increase efficiency in ___ production, megakaryocytes do ___ without ___
|
platelet
replicate nucleus 5 times (32n) cytokinesis |
|
T cells comprise ___% of lymphocytes. ___ (2) are markers for all T cells.
|
65-80
CD2 CD3 |
|
the majority of CD4 cells are in the ___
|
peripheral blood
|
|
the majority of CD8 cells are in the ___
|
BM
|
|
B cells comprise approximately ___% of lymphocytes. ___ (3) are markers for B cells
|
5-15
CD19 CD20 CD22 |
|
___ (2) are markers for NK cells
|
CD16
CD56 |
|
T/F: most circulating lymphocytes come from BM
|
false: most are produced in lymphoid tissue
|
|
hemangioblast gives rise to ___ (2)
|
pluripotent HSC
endothelial cells |
|
HSC gives rise to ___ (2)
|
CMP
CLP |
|
CMP is aka ___. it gives rise to ___ (2)
|
CFU_GEMM
MEP GMP |
|
___ is a marker for HSCs
|
CD34
|
|
bone marrow stroma is composed of (5)
|
fibronectin
hemonectin laminin collagen proteoglycan |
|
___ (2) stimulate HSC differentiation
|
SCF
IL-3 |
|
___ (3) stimulate CMP differentiation
|
SCF
IL-3 GM-CSF |
|
EPO is synthesized by ___ (2). synthesis is regulated in response to ___.
|
kidney
liver oxygen tension |
|
EPO uses (5)
|
autologous blood transfusion
AIDS diabetes myelodysplastic syndrome anemia of chronic renal failure |
|
___ (2) stimulate MEP differentiation into ___ (2) cells.
|
IL-3
GM-CSF MKP EP |
|
___ (2) stimulates MKP differentiation into ___.
|
TPO
GM-CSF platelets |
|
___ stimulates EP differentiation into ___.
|
EPO
RBCs |
|
___ (2) stimulates GMP differentiation into ___ (2) cells.
|
GM-CSF
IL-3 GP MonoP |
|
___ (3) stimulate GP differentiation into eosinophils
|
G-CSF
GM-CSF IL-5 |
|
___ (2) stimulates GP differentiation to neutrophils
|
G-CSF
GM-CSF |
|
___ (2) stimlates MonoP differentiation to ___
|
M-CSF
GM-CSF monocytes |
|
EPO works on ___ stages of RBC
|
late BFU-E and CFU-E
|
|
G-CSF sources (4)
|
stromal cells
endothelial cells monocytes macrophages |
|
G-CSF functions (3)
|
maturation and proliferation of neutrophil progenitors
mobilization of myeloid SCs into PB neutrophil activation and enhanced lifespan |
|
G-CSF applications (4)
|
reduce neutropenic period after chemo
after BMT collection of SCs from PB Kostmann's syndrome |
|
Kostmann's syndrome is a ___ disorder of ___
|
AR
deficient neutrophil maturation |
|
in mammals, interphase lasts at least ___
|
12-24 h
|
|
2 events in G1
|
RNA production
protein production |
|
events in S
|
DNA replication
|
|
events in G2 (2)
|
growth
protein production |
|
mitosis typically lasts ___
|
1-2 h
|
|
___ phases have checkpoints
|
G1
G2 M |
|
mantle cell lymphoma is frequently caused by a ___. this causes the ___ gene on chromosome ___ to ___.
|
11-14 translocation
cyclin D1 11 be overexpressed |
|
___ is a family of kinases regulating mitosis and meiosis
inhibition of it is a potential ___ therapy |
aurora
cancer |
|
aurora kinase A phosphorylates ___
|
centrosome
|
|
aurora kinase B phosphorylates ___, causing ___
|
centromere
attachment to mitotic spindle |
|
aurora kinase C functions in ___
|
meiosis
|
|
2 apoptosis pathways
|
death receptor (extrinisic)
mitochondrial (intrinsic) |
|
death receptor apoptosis is triggered via ___ (2)
|
Fas
TNFR |
|
intrinsic apoptosis pathway is triggered when ___ release ___ which binds to ___. these aggregate to form ___, which activates ___.
|
mitochondria
cytochrome c Apaf-1 apoptosomes caspase 9 |
|
mitochondrial release of cytochrome c is suppressed by ___, on chromosome ___.
|
Bcl-2
14 |
|
follicular lymphoma is triggered by a ___ which causes overexpression of ___
|
14-18 translocation
Bcl-2 |
|
2 pro-apoptotic members of Bcl-2 family
|
Bax
Bak |
|
p53 causes transcription of ___ after ___, which increases ___.
|
Bax
DNA damage mitochondrial permeability |
|
___ (2) inhibit Bcl-2 and ___ apoptosis
|
Bid
Bim promote |
|
Bad, Bid and Egl-1 are special in that they only have ___. they are pro/anti apoptotic
|
BH3 domain and no other BH domain
pro |
|
___ (2) are BH-3 mimetic drugs
|
ABT-737
ABT-263 |
|
___ (5) are bound by type 1 cytokine receptors
|
EPO
TPO G-CSF GM-CSF ILs |
|
type 1 cytokine receptors lack ___ and use ___ for signalling
|
cytoplasmic Y kinase domain
JAK-STAT |
|
JAK binds to the receptor by its ___ domain. before the ligand binds, the ___ domain is inhibited by the ___ domain. after the ligand binds the inhibition is lost because of ___.
|
FERM
JH1 JH2 conformation change separating JH1 and JH2 |
|
a mutation in ___ can cause constitutive activation of JAK2 because ___, and is implicated in (3)
|
JAK JH2 domain (V617)
JH2 inhibitory function is lost polycythemia vera essential thrombocythemia idiopathic myelofibrosis |