Repair of CNS injuries by transplantation of OECs Flashcards Preview

Stem Cell and Regenerative Medicine > Repair of CNS injuries by transplantation of OECs > Flashcards

Flashcards in Repair of CNS injuries by transplantation of OECs Deck (58):
1

what is so special about olfactory system?

it is the only area where neurons are continuously formed thoughout adult life. The newly formed axons are accompanied by special type of glia and grow into the CNS

2

what type of glia accompany the forming axons?

olfactory ensheathing cells

3

what was the general thought behind the OEC experiments?

- can you transplant OECs into regenerating axons to regenerate and restore function

4

what 4 injury models can be used for testing OECs?

- corticalspinal tract lesions
- spinal cord hemi-section
- spinal roots lesion
- optic nerve transections and glaucoma model

5

why are the cortical spinal tract region used as a model?

- there is an antibody that you can use so that you can easily measure the injury to the tract and how it regenerates

6

how did they functionally check the outcome of CST injury?

- they lesion the rat and then put food on the platform so that a paw can reach through and take the food through the gap - - normally the rat will reach through with both hands
- they remove one side of the cortical spinal tract (it is present on both sides) so that they can compare to the control on the other side of the spine
- you see that the the non lesioned paw side is only used
- this shows that after this lesion the rat cant reach through and take the food with that paw

7

what are the two sources of OECs?

olfactory bulb and olfactory mucosa

8

what is the marker of OECs?

P75

9

what mixture of cells is the best in terms of OECs?

culture for 2 weeks with a mixture ofFurthermore, it has been reported that a 50:50 ratio of OECs with olfactory nerve fibroblast-like cells, rather than pure OECs produces optimal transplant-mediated repair- but some people find that purification is best

10

before you transplant, what is important n terms of labelling?

you transact with GFP marker so that you can recognise them in the transplant

11

how long did it take after transplantation did it take for the axons to regrow ?in the corticosinal tract experiments?

around 3 weeks before was almost back to normal

12

after they had transplanted and found improved function, how can you prove that it is due to improved on regeneration?

you use mmunostaining to label the CST fibres. you see that in the control thy stop at the edge of the lesion but when you transept yo see that the axons grow through the transplant and back to the original tract ad form the terminal field and they are being myelinated by the OECs and oligodendrocytes

13

how are OECs similar to SC?

they myelinate axons

14

what is a hemisection?

cut had of the entire spinal cord

15

how can you ensure that the cells dont move away from the area of cut?

you can put them in a gel and be retained in that region

16

how did they measure the effects of OEC transplant onto a hemisection injury?

they added OECs in a gel and then measured the spriatory rythym from the phrenic nerve - they found that the unrelated there was no activity bt in the treated the rhythm was restored and spontaneous

17

what is the problem of wound son the DRG?

a glial scar formed by astrocytes

18

how did they investigate the role of OECs n DRG damage? including how they tested for functional repair?

they cut and then transplant he OEC and label the axons- in the control you never see any axons crossing the border between the doral horn and dorsal cord but in the transplant and you can see that the axons cross the border.
- they looked at the rat moving up the poles of a cage.
- if you cut three roots C6-T1 you see a deficit in climbing and mistake made when climbing the bars.
you see with the transplant into the root that you get a increase in mean grasp score increased from 0-4 and the wild type is 7
they record from the cord dorm and cuneate and fun that the response to stimulus comes back (?)
- when you label with GFP you see that when you put cells in the dorsal root then they are more likely to bridge the gap to the spinal cord which doesn't happen in controls

19

how do they create a model for retina ganglion cell transection ?

- they add a cut to the optic nerve

20

what is normally seen when the optic nerve is tansected?

axons are unable to regenerate across the cut and they actually retract 8 months after cut in the rat- but here are some remaining in the cut area- very few axons

21

what happens when you put OECs into he region of optic nerve cut?

you see the axons crossing the cut region of injury and they are brought back to injury tract originally there

22

what stimulated them to look at the role of OECs in repair after glucoma ?

- they saw that it could promote the repair of OECs

23

where did they inject the OECs for the glucoma model study? what idd they see?

into the visual disc- they migrate into the retina na down into the optical nerve region. they also ensheath the RGCs and allow them to regenerate

24

how did they mimic the intraocclar pressure caused in glaucoma? what did they find?

the injected magnetic microphones into the anterior chamber and recorder the IOP using a tonometer- found the beads increased the pressure . The OECs could not prevent the pressure but the found that the number of axons were increased in the OECs transplanted into the optic disc can reduce the loss of RGC axons caused by raised IOPe presence of IOP compared to without them this is not a clinical model because you inject the OEC before beads

25

have OECs been used in humans?

- you can culture human bulb OECs
- they implanted this into the site of injury in the spinal cord
- they found that after 3.5 years and a half he could cycle around on a bike!

26

name two highly occurring cause of non healing skin wounds

atherosclerosis and pressure ulcers

27

why is looking at model organisms not that helping for wound heeling

- mode organism show a lot of variety in their abilities to repair wounds

28

what is the first response to wounds?

- the clotting cascade forms a fibrin clot. Platelets trapped in the clot also release growth factors and cheekiness into the local wound environment

29

in terms of inflammation, what is thought to be part of the cause of chronic wounds?

- they may be stuck in the pro-inflammation phase which become chronically activated: there is a continual competition between inflammatory and anti-inflammatory signals leading to a misbalanced environment for proper wound healing to occur.

30

in terms of cells, which have bene implicated in chronic inflammation in chronic wounds?

- proinflammatory infiltrates composed largely of neurotrophils and macrophages contribute to delayed healing in chronic ulcers

31

the deregulation of which prinflammatory cytokines have bene implicated in chronic wounds and were are these thought to come from? what do they do?

- IL-1beta and TNF-alpha, from macrophages and neutrophils they prolong the inflammatory response
- they are increased in chronic wounds and lead to elevated metalloporeinases hat degrade local ECm and prevent migration

32

what exogenous factor promotes increased presence of pro inflammatory cells?

- an increased bacterial load

33

how are proteases implicated in wound healing?

Unlike the acute wound-healing process, where tissue proteases are normally under tight regulation, it appears that in a chronic wound, disruption of the produc- tion and activation of proteases plays a role in wound pathogenesis. The proteolytic unbalance may be a consequence of the aforementioned faulty regulation of inflammation and/or microbial contamination. It has been shown that matrix metalloproteinases (MMPs), such as collagenase and gelatinases A and B, are elevated in chronic wound fluids when compared to acute wound fluid

34

how are stem cells implicated in chronic wounds?

Recruitment of bone marrow and endothelial progenitors to the site of injury is coordinated by specific chemokines, which have been shown to be depleted in conditions that contribute to compromised healing response, such as aging and diabetes. Furthermore, frequent cycling of epidermal stem cells in patients with chronic wounds can lead to depletion of local stem cell populations. Compromised function of local and systemic stem cells and progenitors may play a considerable role in pathology of chronic wounds.

35

how is angiogenesis implicated in chronic wounds?

nadequate local angiogenesis is considered a very likely contrib- utor to the impaired healing of DFUs (3). Proteins with antiangiogenic properties, such as myeloperoxidase, exhibit higher expression levels in chronic wounds of diabetic patients as compared to acute wounds, whereas angiogenic stimulators, such as extracellular superoxide dis- mutase, are generally decreased

36

how are senescent cells implicated in chronic wounds?

One hypothesis is that cells, fibroblasts in particular, become prematurely senescent within a chronic wound setting. Senes- cence caused by oxidative stress might also drive uncontrolled fibro- blast proliferation and keloid formation (56). Senescent fibroblasts and keratinocytes secrete MMPs 2, 3, and 9, and might therefore exert an antifibrotic effect (57). Moreover, senescent keratinocytes have been documented to secrete the antiangiogenic factor maspin (58), which may also be detrimental to repair. They are also pro inflammatory

37

what growth factors can be added to wounds and have been shown to promote wound healing?

FGF-2, KGF-1- not VEGF though

38

what are 2 arguments against using growth factor application?

Given the complexity of the multicellular tissue repair response (Fig. 2), it is not surprising that therapeutic delivery of a single factor and/or cellular component often only achieves limited efficacy in stimulating healing of chronic wounds. Furthermore, recent studies indicate that cells within the chronic wound may lack other aspects of the molecular milieu that enable an appropriate response to growth factor stimuli, such as down-regulation of epidermal growth factor receptor (EGFR) and TGFb receptors as well as SMADs

39

what is the most overt sign of chronic wounds?

failure of wound reepithelialisation

40

what are the first genes to be upregulated at the wound edge epithelium? what will be the role of these genes?

- fos, ap-1, jun
- cell proliferation, epidermal migration of a leading tongue of keratincoytes at the interface between the scab and the healthy wound granulation tissue

41

what needs to happens for the keratoncytes to migrate during wound healing

- some interns are switched off and others are turned on such as Beta1 integrin

42

when repeithelialisation occurs, where do these stem cells me from it is thought?

he new keratncoyets are thought to come from the stem cell dense budge of hair follicles. ad from the non bulge region follicular cells.

43

where do the wound fibroblast population come from, what showed this?

- fluor MSCs after intravenous injection were reported to contribute tot the wound fibroblast population - these are from the bone marrow normally

44

what studies link inflammation to scarring?

Studies of repair in embryonic and fetal mice and also human patients undergoing fetal surgery have indicated that, before the onset of a wound inflammatory response, immature tissues are capable of scarless healing (99, 100). Inflammation might therefore be a cause of wound fibrosis. Indeed, mice lacking the ETS family transcription factor PU.1 (and thus not able to generate any leukocytic lineages) are able to heal wounds effectively as neonates—and do so without subsequent scarring, unlike their wild-type littermates

45

what are the initial sources of inflammation?

Some of the earliest signals include factors released by degranulating platelets (23) and by damage- and pathogen-associated molecular patterns (DAMPs and PAMPs, re- spectively) where cells are damaged and microbes gain access
- s a wound gapes open and then begins to contract, focal adhesion kinase/extracellular signal–regulated kinase (FAK-ERK) leads to activa- tion of chemokine ligand 2 release by wound fibroblasts, which, in turn, draws in a larger inflammatory response

46

why are flies good for regeneration studies? whats bad?

- good for tissue labelled- membrane labelling - translucency
- they only have a single immune cell lineage

47

how have stem cells been used in wound repair? (2)

- Clinical studies have shown that bone marrow– and adipose tissue– derived MSCs can augment the repair process when applied locally to chronic skin wounds
- Recent developments in reprogramming skin and other differen- tiated cells into induced pluripotent stem cells (iPSC) provide a new cell source that can potentially be used for therapy. It has been shown that human skin equivalents can be created entirely from fibroblasts and keratinocytes generated from patients’ iPSCs, and that healthy cells can be generated from reprogrammed cells from patients with RDEB

48

what are the 5 steps of wounding?

haemostasis, inflammation, proliferation and migration, followed by scar tissue remodelling

49

how long after injury is cx43 upregulated? what is this correlated with?

- 6 hours
- keratinocytes crawling adopting a migratory phenotype as they crawl across the wound bed to close the epidermal breach

50

what is upregulated in the leading edge keratinocytes during migration?

cx30 and 26

51

what is the process by which cx43 is down regulated thought to be?

A role for protein kinase C has also been proposed in phosphorylating Cx43 serine 368 at the wound edge in order to decrease its communication,

52

why is loss of cx43 from the migrating cells thought to be deseriable? (2)

- Cx43 can bind to an array of other junctional and cytoskeletal proteins, either directly via a PDZ domain or indirectly via other proteins such as membranous Cadherins, Zonu- lar Occludin-1 (ZO-1), α- and β-catenin, as well as cytoskeletal mi- crotubules and actin. Such interactions may affect both cell adhesion and cytoskeletal dynamics and therefore cell migration and wound healing.
However, some of the interactions are with tran- scription factors such as β-catenin, and binding to it may keep β- catenin at the cell membrane, preventing it from influencing gene ex- pression. Indeed, it has been proposed that Cx43 forms the centre of a protein complex or “nexus” acting as a master gene that can influence expression of other over 300 other genes

53

where is cx43 upregulated, why is this thought to be (mediated)?

within the first few hours it is upregulatedin the endothelial cells of blood vessels as they become inflamed- The upre- gulation of Cx43 is likely to be brought about by the proinflammatory signals being released at the wound site and this correlates with the blood vessels becoming leaky to leukocytes, proteins and fluids which in turn cause the dermis to swell.

54

t are the steps of inflammation?

- mast cells and degranulating platelets form a fibrin clot and release PDGF which attracts neutrophils which express more inflammatory signal which in turn recruits monocytes that transform into macrophages

55

what did people think about he inflammation response initially and what do they think now?

1. he production of a strong inflammatory response is thought to provide the signals to stimulate wound repair by transforming wound edge fibroblasts and keratinocytes into a migratory phenotype that will crawl forward to close the wound and fill the wound bed with granulation tissue
2. This suggests that far from being es- sential for triggering the onset of wound healing the inflammatory re- sponse, it may in fact be contributing to fibrosis and scar formation [57]. Indeed large numbers of neutrophils at a wound site may do more than just kill bacteria; the release of free radicals designed to kill bacteria may also kill healthy cells in the intact surrounding tis- sues

56

how does application of nexxigon affect neutrophils?

neutrophils both in and around the wound sites on days 1 and 2 after injury are reduced following application

57

draw a diagram to summarise the affects of antisense cx43

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58

what evidence is there that the neutrophils and oocytes may not be needed for repair?

In the absence of both cell types, the repair of small wounds can still occur, and the scarring response is even less30.