Lecture 11: Stem Cells in Tissues Flashcards
(wasn’t at lecture so may need to look into more)
Somatic SC characteristics
Rare
In human bone marrow
Tissues renewed by stem cells
High turnover Natural Easily damaged Common/all? Include: Brain Gut Skin Bone marrow
Haematopoietic system
bone marrow (hematopoietic stem cell) -> common lymphoid progenitor (->B cell and T cell -> plasma cell and activated T cell), common myeloid progenitor ->granulocyte/macrophage progenitor, megakaryocyte/erythrocyte progenitor (-> neutrophil, eusinophil, basophil, monocyte (granulacytes)->mst cell, osteoclast, macrophage) ->magakaryocyte and erythoblast (->platelets and erythrocyte) (diagram slide 7)
HSC origins
- Generated during embryonic development
- Persist throughout life
- Replace blood cells
- First HSC detected in the AGM region (Aorta, Gonads, Mesonephros)
- Then enter circulation and colonise the liver
- Finally reside in the adult bone marrow
Bone marrow transplantation = HSC transplantation
(slide 8 and 9)
Skin Structure
-epidermis (keratinocytes
-dermis (fibroblasts, ECM)
-subcutaneous fat
(more in notes diagram slide 10)
Epidermis: layers of keratinocytes
-cornified layer
-granular layer
-spinous layer
basal layer: proliferation, stem cell niche
(11)
Keratinocyte differentiation in the epidermis
-BASAL layer of the epidermis is the proliferative compartment.
-BASAL layer contains the Stem Cells which give rise to transient amplifying cells. Transient amplifying cells provide the non proliferative terminal differentiating keratinocytes.
(EGFR activity inhibits Notch, asymmetric division promotes the switch from basal layer cell to spinous cell, high notch activity inhibits integren gene expression???)
-Keratinocytes terminally differentiate as they migrate up through the epidermis
-As keratinocytes differentiate and take on new characteristics they change their molecular profile
The hair follicle
-sebaceous gland region
-bulge region
-intermediate region
-bulb region
(look notes slide 14)
Clonogenic keratinocytes
-are long-term multipotent stem cells
-Two locations for SC
-Contribution to all hair lineages, sebaceous gland and epidermis (transiently)
-Long life span
(15)
How do you get Long-term persistence of hair follicles generated from a single multipotent stem cell?
- one cell->in vitro expansion->grafting->1 cell-> in vitro expansion (karyotype) -> grafting (dermabrasion)
- notes 16 and 17
The gut
- Two stem cells described one rarely dividing, one faster
- Give rise to transit amplifying cells
- TA cells differentiate as they move up the crypt
- Movement apparently driven by cell division and active migration
- Cells are shed at tip of villus
- Main cell types: Enterocytes, Goblet cells, Paneth cells, Enteroendocrine cells (18)
Mouse neural stem cells (SVZ)
-SVZ astrocytes are adult neural stem cells (B)
-Transit amplifying cells (C) divide rapidly and generate
Neuroblasts (A) which migrate along the Rostral Migratory Stream to the Olfactory Bulb (19)
Stem Cell Niche
don’t get this slide (20) look over