Reverse Terms Flashcards

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1
Q

in between the koller’s sicker and area opaqa

A

posteior marginal zone

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2
Q

-Wnt binds to frizzled receptor which interacts with ROR -activates DTI (phosphoralation) interacts RoA & Rac -RoA activates kinase involved with cytoskeleton changes 9for cell moments) -cells told to remain/divide in same plane

A

Non-Canonical (B and C)

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3
Q

•Belongs to the category of non-canonical pathway. • Some Wnt molecules can activate DSH through the Frizzled receptors paired with ROR. • Through this DSH activates Rho-GTPase. • Rho-GTPase activates the kinases that phosphorylate the cytoskeletal proteins that alter cell shape and movements.

A

Planar Cell polarity (PCP) Wnt Signaling pathway

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4
Q

Building of 3D structure, generation of the form that we see.

A

Morphogenesis

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5
Q

Sorting of cells: Homotypic cell adhesions,

A

Cadherins

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6
Q

•Adherin junction (where one attaches to the other cad herein) basis on forming epithelium •ECM (extra cellar membrane) around cells •interns NB for cell-ECM interactions •TMP (trans membrane protein) with an alpha and beta subunit •2 signalling: outside-in, inside-out •when signalling received, alpha beta subsets are rendered apart. Heads no longer bent but straight •70 armstrong (70ºA) •inactive intern is close •

A

Integrins

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7
Q

is Important in organogenesis as well as cancer biology. • Cancer initiates as a epithelial cancer … later metastasize to different locations • Epithelial sheet forms a water-proof covering, bend-sheet forms tube, etc. • Epithelial cells are attached to each other through adheren junctions and the the basal lamina through integrins

A

Epithilial-Mesenchyme Transition (EMT)

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8
Q

Limb bud-tip formation

A

Apical Ectodermal Ridge (AER)

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9
Q

All three zones that differentiate as cells leave the progress zone. As limb bud grows, the cell fate is established.

A

Theory of posterior distal axis formaition: Progressing zone model.

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10
Q

All regions are pre-established. As time progresses, limb bud grows and regions (refer to pic) expand. Early stage small, late sage large in size.

A

Thoeyr Early allocation and progenitor expansion model

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11
Q

elimination of certain chromosomes from cells that form somatic tissues

A

chromosomal diminution

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12
Q

number of fates cells can take

A

potency

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13
Q

cells that can form every cell of embryo (3 layers, etc) and cells of placenta

A

totipotent

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14
Q

cells that can form cell of all 3 germ layers but not placenta

A

pluripotent

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15
Q

cells derived from embryo or adult committed to form small component of cells (hematopotent stem cells = present in bone marrow and capable of forming all blood cells)

A

multipotent

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16
Q

cells that can take up only one or two fates

A

uni/bi potent

17
Q

micro environment in which these stem cells can exist

A

Stem Cell Niche

18
Q

cells can keep making more cells or go on to commit to differentiation

A

Single Cell Asymmetry

19
Q

in order to keep up the population, some cells are more prone to make more and some are more prone to commitment

A

Population Asymmetry

20
Q

-T helper cells are Cd4 (markers on them) -T cytotoxic cells CD8 markers on them -stem cells have specific surface markers -cell foes through resivor one at a time. Excited by laser and florescent light detected by photomultiplier tube -certain changes (that’s related to surface markers) and separated into fractions

A

Fluorescence activated Cell sorting (FACS)

21
Q

•UV a mouse to destroy it’s BM cells •if left alone it’ll die •inject with normal BM cells •it survives •isolate the hematopoietic stem cells

A

Repopulation Assay:

22
Q

-inducers are ligands -can figure out potency of cell population (number of fates cell can take up) -induce cells and wait to see what fates they take.

A

In Vitro Induction Assays using Stem Cells

23
Q

•EScells can be differentiated in somatic cells then reprogrammed to
__________ by TF such as Sox2 and Oct4 •Regenerative Medicine: Disease treatment Organ repair

A

induced pluripotent stem (iPS) cell

24
Q

•multipotent stem cell undergoes differentiation into an number of things it could be, or unipotent stem cell becomes differentiated into the specific one thing •specific replacement of lost tissues •Ex: blood cells (haematopoiesis); digestive tract epithelium; hair shafts; planarian flatworms

A

Stem cell mediated regeneration

25
Q

full differentiated cell undergoes dedifferntiation then this multipotent undergoes differentiation •“dedifferentiation” and “re-differentiation” of cells at wound sites. – De-differentiation is differentiated cells form relatively undifferentiated mass of cells that later re-differentiates to form new structures. – Ex: amphibian and insect limbs

A

Epimorphosis

26
Q

•transdifferentiate into different cell types. Example, epithelium becomes neuron. •Repatterning from existing tissue with no new growth •Ex: hydra regeneration

A

Morpallaxis

27
Q

•different cells are induced to divide and you increase the number, but they maintain their differentiated functions. Each cell produces cells similar to itself. •re-patterning of existing tissues without new growth. Ex: mammalian liver

A

Compensatory Regenration

28
Q

normally supplied by limb nerve •Limb is denerved 7 d later amputed. •5d later ? is electroporated into the limb blastema. •Control newt not supplemented with ? limb remained as a stump. Supplementation of ? restored the ability to regenerate the limb.

A

nAG

29
Q

Before: •CSL TF is on the enhancer of Notch regulatory genes and binds the repressors Activation: •ligand (ex. delta) binds to extracellular domain of Notch on an adjacent cell •causes shape change in intracellular domain of notch •activates protease •protease cleaves notch •intracellular region of notch enters nucleus and binds to CSL •intracellular notch region displaces repressor and binds activators of transcription (ex.p300) •activates CSL can transcribe target gene

A

Notch-Delta Signaling Pathway

30
Q

-cut on side of organism, then suture together -after 2 weeks the share a circulatory system -inflict injury on one other them -if hurt old: muscle cells regenerate back together like it was a young -young has all the paracrine factors

A

Parabiosis

31
Q

-insulin growth factors activate IGF receptors -which activate P13 kinase -activates AKT -P TEN inhibits AKT -If AKT inhibited blocks Foxo and activates MTORC1 -leads to functional decline go post-mitt tissues and stem cells, therefore aging

A

Insulin Repair Pathway

32
Q

In planarian flatworms, regenera’on is a kind of stem-cell
mediated event, and occurs in a way that suggest a
morphogen gradient is at work in the regenera’on that is
observed.
• At the cut surface ______ (pluripotent stem
cell) direct development of the missing structures—heads
make tails, and tails make heads.

A

clonogenic neoblasts

33
Q

Formation of the terminal regions of a Drosophila
embryo by torso signalling. The repressor shown in
(B) is the product of the gene ____

A

Capicua.

34
Q

what inhibits the primitive streak in chickens

A

Cerberus

35
Q

Drospholia had legs, wings and in the methathorax ____

A

blankers or Halters