Lecture 7: Somites Flashcards

1
Q

what is the tissue organisation of the germ layers in triploblastic animals

A

cells from the epiblast/primitive ectoderm move towards a blastopore/primitive streak = generates endoderm first which replaces the extrabonic hypoblast
cells leaving epiblast after settle between the endoderm and ectoderm = mesoderm
cells that don’t become internalised settle on the outside and become the definitive ectoderm

epithelium - simple/non-layered/stratified mono-layered
endothelia - cuboidal/long with diff thickness
transitional - changes from one layer to the next
polarised - basal side anchored on extracellular matrix basement membrane - cells linked with demosomes
cilia on opposite side

mesynchime - loosely held together cells

epithelial and mesenchyme cells can occur in any of the 3 germ layers

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2
Q

what will become of the ectoderm endoderm

A

ectoderm
neural tube w forebrain, midbrain, hindbrain + spinal cord
neural crest cells
epidermis

endoderm
alimentary gut
canal
air sacs/lungs

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3
Q

how does the axial mesoderm signal to the surrounding tissues

A

produces Shh and noggin

the dorsal neural tube and surface ectoderm release Wnt signals, the lateral mesoderm produces BMP signals

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4
Q

how does trunk paraxial mesoderm segment into somites

A

metameric segmented organisation

somites form caudal to inner ear

segmentation is visible in adult in vertebral column

human spondylocostal dysostosis = malformed vertebral column

initially the paraxial mesoderm is laid down as a mesenchyme on either side of notochord
paraxial mesoderm forms epithelial balls of cells
somite formation progresses in rotro to caudal or anterior to posterior direction
somites appear at regular intervals of 90 mins in chicken or 2hrs in mice 30 mins in zebrafish

regular segmentation is regulated by a negative feedback loop = molecular clock oscillator and a signal to tell cells to go ahead and organise themselves int a discrete unit or a wave front

auto regulatory loop of the notch delta signalling between cells that touch
Fibroblast growth factor Fgf8 levels fall below a threshold = signal

high fgf = immature state = inhibits segmental boundary formation

low threshold = determination front

segment boundaries are formed when cells in a certain phase of oscillation encounter the determination front

new cells are added to the caudal end
somites bud off rostral end all the time

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5
Q

basic function of somites

A

making segmented muscle myotomes for left right undulating movements
dorsal dermis

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6
Q

formation of somites

A

specification &proliferation of mesoderm precursors

segmentation of the paraxial mesoderm
delta notch fgf8

epithelial somite formation
wnt 6 inclusing paraxis

patterning & differetiation
epithelialisation - cells must condense and undertake a mesenchyme to epithelium transition requiring the increase of cel adhesion formation of tight junctions

epithelial somite formation is regulated by Wnt6 signalling from the surface ectoderm activating the transcription factor Paraxis and the two related transcription factors Pax 7 and 3

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7
Q

somite patterning

A

induction of dermomyotome (holds the precursors for the dorsal dermis and muscle) and the myotome

myotome (contractile muscle) = subdivided into deep muscles of the back called epaxial muscles from the medial lip
from the lateral lip form hypaxial muscles abdominal and limb muscles
cells from the centre contribute to epaxial and hypaxial muscle

sclerotome (delivers the vertebral column and ribs

pstterning depends on extrinsic cues = appositional induction

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8
Q

how is the mesoderm subdivided along the mediolateral axis

= dorso-ventral axis into axial, paraxial, intermediate and lateral mesoderm

A

primitive streak will form the neural plate = neural tube and axial mesoderm the notochord

paraxial mesoderm is the source of the axial skeleton
segments into somites and give rise to skeletal muscle, dorsal dermis + vertebrae and ribs

intermediate mesoderm - anlagen kidney and gonads

lateral mesoderm delivers peritoneum, skeleton outer muscular layer of gut, heart, blood

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9
Q

somites

A

reiterated morphologically alike units

epithelial balls of cells

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10
Q

muscle formation in the embryo from paraxial mesoderm = epithelial somites by mesenchymal-epithelial transformation

A

sorsal smite = epithelial dermomyotome

myotome forms first from the lips of the dermomyotome later from ingressing cells from the centre
remaining cells from dermomyotome = dermomyatome forms the dorsal dermis
cells from the medial wall of the somite detach and differentiate = primary myotome = scaffold
express specific muscle regulatory factors
cells from all 4 libs contribute = secondary myotome
post mitotic
cells from centre = tertiary myotome
act as stem cells
self renew into satellite cells or differentiate and make the bulk of fetal and adult muscle

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11
Q

tissues interactions in somite patterning to secrete patterning signals

A

dorsally
surface ectoderm and neural tube

ventrally notochor floor plate and endoderm
laterally intermediate and lateral msodem

all secrete signal

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12
Q

molecular markers for somite compartments

A

Pax3 - dermomyotome lips
MyoD - myotome
Pax1 - sclerotome
Labx1 - lateral dermomyotom

can be used as early molecular
markers for somite differentiation

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13
Q

molecular markers for somite compartments

A

Pax3 - dermomyotome lips
MyoD - myotome
Pax1 - sclerotome
Labx1 - lateral dermomyotom

can be used as early molecular
markers for somite differentiation

the dorsal neural tube and surface ectoderm release Wnt signals, the lateral mesoderm produces BMP signals

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14
Q

Dorsal patterning Wnt

A

the dorsal neural tube and surface ectoderm release Wnt signals

removal of neural tube and ectoderm leadds to loss of Pax3 and MyoD and expansion of Pax1 expression
Loss of Wnt signalling results in reduced muscle formation

Wnts from dorsal neral tune and ectoderm are require for dermomyotome and myotome formation and the restriction of the sclerotome

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15
Q

Antagonistic action of signals

non co operatiely

A

Shh vs Wnt
controls the subdivision of the epithelial somite into ventral sclerotome and dorsal dermomyotome

notochord and floor plate secrete ventralising
Shh
induces sclerotome Pax1 and suppresses dermomyotome

\Dorsal neural tube and epidermal ectoderm secrete dorsalising wnts
induces dermomyotome Pax3 and supresses sclerotome

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16
Q

synergistic somite patterning signals

A

Noggin vs Bmp
controls myotome formation and mediolateral somite patterning

formation of the hypaxial myotome abdominal muscles (BMP+ WNT)

SHH+WNT=epaxial myotome deep muscle of the back

ventral Shh and neuraltube derived Wnt induce the medial, epaxial myotome - gives rise to deep muscle of the back

ectoderm derived wnt and bmp4 from the lateral plate induce the lateral and hypaxial myotome =abdominal and limb muscles

17
Q

how do vertebrae along the rostral caudal axis become different

A

sclerotome fate
each vertebra is formed from the caudal posterior part of one sclerotome and the rostral/anterior of the next in line
vertebra are initially formed as cartilage before ossification turns them into bone

hox genes encode a particular type of homeodomain transcription factors an are organised in clusters
expressed in time sequence in line w their order in the cluster = temporal collinearity

combinatorial expression of Hox gene provides somites and the vertebrae developing from them - positional info an identity

alteration of hox gene expression changes cell tissues positional info

shapes into what would be found at a diff location
homeotic transformation

hox loss or gain leads to homeotic transformation

when lost = the more caudal position is lost
somites developing from this position have a more anterior shape