Unit 8 (quizzes and cards)

what do epiblast cells become

liver, bile duct, and pancreas cell

what can some nodal make

epiblast

what does epiblast make

mesendoderm

what happens if Bmp and fgf present with mesendoderm

they repress nodal and turn into mesoderm

what is formed since posterior region has high Bmp, fgf, and Wnts

MG-HG to turn into intestines

what does a mid level of Bmp, fgf, and Wnts make

PRG turn to pancreas and hepatoblast

what does low level at anterior of Bmp, fgf, and Wnts do

AFG turn into thyroid and lung

what turns into the gut

large yolk sac

what starts at 3 weeks

kidney deveolpment (mesonephron)

where does liver tissue only form in mouse liver endoderm

only form when near cardiac mesoderm

what does hepatic region express

alpha-fetoprotein and albumin

what is the hepatic region formation influenced by

being near heart

where is supression to ensure hepatic region form in certain spot

cardiac mesoderm, mesenchyme cells, ectoderm, and notochord

what is in the gut and is expressed from touching aorta and vitelline veins

Pdx1

in ventral endoderm what does retinoic acid suppress

Wnt and shh, which allow Pdx1 to form, going to pancreatic bud, then to exocrine progenitor which turn into ductal or acinar cell

what happens if Ngn3 and fgf10 is expressed pancreatic bud

turn into endocrine proginator and into beta, gamma, alpha, or PP cells

what if fgf, Bmp, foxa1 and 2 expressed into hepatoblast

turns into hepatocyte or cholanglocyte

how many pharengeal pouches on 1 side

4

what does sox17 do

specfiy structures in digestive tube

what does pdx1 and cdxc do

specify small intestine

what does hox do

specify liver

what does cdxa do

colon, rectum, large intestine

what happens is mesenchymal cells express Barx1

then sFRPs activated which inhibit Wnt which turn into stomach

what happens if there is sox9 and NKx2

form spinchter muscle

what if there is no Barx1

expresses Wnt and turn into intestine

what makes sure the gut is wrapped correctly

dorsal mesentary

where does the respiratory diverticulum (laryngotracheal groove) with the foregut develop

on the side of the foregut

where do lungs form

on side of foregut

how is esophogus made

with Barx1 expressed it makes sFRPs that block Wnt

what is ciliated respiratory epithelia formed with

Wnt expressed

where does immune system relay signal from

embryonic lung

where is SP-A secreted

into amniotic fluid

what does SP-A do when secreted into amniotic fluid

activates macrophage and migrate to interlukin-1B

where does interleukin-1B do

to cyclooxygenase 2 and then to prostaglands which cause uterine contractions

Endoderm

Two primary sources: Migrating epiblast cells during gastrulation through the primitive streak → definitive endoderm; Visceral endoderm (hypoblast) → contributes especially to anterior structures and foregut.

Mouse model evidence

Visceral endoderm marked with GFP; Epiblast cells randomly labeled with red dye; Over time, red-labeled epiblast cells migrate through the primitive streak and replace visceral endoderm.

Pathway

Epiblast cells are maintained by Nodal, BMP, and WNT signals; High Nodal levels → conversion to mesendoderm; Even higher Nodal levels → specification to definitive endoderm; FGF and BMP inhibit Nodal, diverting mesendoderm cells to mesoderm fate instead.

Mesendoderm

Bipotential precursor that can become either mesoderm or endoderm depending on signal strength.

Anterior-Posterior Gradient

Posterior (high signal levels) → Midgut-Hindgut (MGH) → intestines; Intermediate signal levels → Pancreas and hepatoblasts (liver); Anterior (low signal levels) → Foregut → lung and thyroid tissues.

Anatomical logic

Lungs (top), liver/pancreas (middle), intestines (bottom); The gradient corresponds to natural anatomical positioning.

Paracrine signal gradient

Defines regions: Anterior Foregut (AFG) → lung, thyroid; Posterior Foregut → liver, pancreas; MGHG (Midgut/Hindgut) → intestines.

Morphogenesis of the Gut Tube

Cross-section (A) and sagittal section (B) show embryo orientation; Key structures: paraxial mesoderm, intermediate mesoderm, notochord, neural plate/tube; Development starts with flat endoderm sheet beneath the embryo.

Formation of portals

Anterior Intestinal Portal (AIP) and Caudal Intestinal Portal (CIP) form at either end; These portals fold and meet in the center to close off the gut tube.

Yolk sac transformation

Initially large and balloon-like; Eventually gets pinched into a narrow, elongated gut tube.

Timeline of Gut Formation

~3 weeks: Formation of CIP and AIP; Yolk sac begins to fold inward; Early kidney structures appear (mesonephros); ~4 weeks: Further pinching off of yolk sac; Formation of stomach, liver, pancreas (anterior/midgut); Gut tube forming clearly as a distinct structure.

Heart development

Is proximal to liver/pancreas due to local signaling.

Kidney development

Starts along the gut tube near the notochord.

Gut tube connection

Connects the mouth (anterior) to the anus (posterior).

Yolk sac degeneration

Leaves a continuous gut tube.

Pancreas Development

Origin: The pancreas forms from two separate diverticula (outpouchings of the foregut endoderm)—the dorsal and ventral pancreatic endodermal buds.

Fusion of pancreatic buds

At day 30 post-fertilization: both buds are visible; By day 35: the ventral bud migrates around to meet the dorsal bud; At day 40 (week 6): they fuse into a single pancreas.

Duct Formation

Normally, the dorsal duct regresses, leaving a single pancreatic duct; In ~10% of individuals, both ducts persist without apparent functional consequence.

Sonic Hedgehog (Shh)

Usually promoted by the notochord in the ectoderm; Repressed in the endoderm where the pancreas develops, via FGF2 and Activin from the notochord.

PDX1 Gene

Expressed in areas of gut endoderm near the aorta and vitelline veins; Crucial for pancreas development; defines where pancreatic buds will form.

Chick vs. Mouse

Chick embryos: three lobes initially due to two vitelline veins and the aorta; Mouse embryos: only two lobes persist due to loss of one vein and its associated lobe.

Lineage Differentiation

Dorsal endoderm → pancreas only; Ventral endoderm → pancreas or liver, depending on signals.

Exocrine progenitors

Split into ductal and acinar cells.

Endocrine progenitors

Develop into β-cells, α-cells, γ-cells, and PP cells via NGN3.

Positional Signals

Liver-forming endoderm must be near the cardiac mesoderm.

FGF1/FGF2

From cardiac mesoderm, block inhibitors from notochord, mesenchyme, ectoderm to enable liver-specific gene expression.

Markers

Liver-forming tissue expresses alpha-fetoprotein and albumin.

Repression of liver fate

Occurs where the endoderm is too close to ectoderm, notochord, or other mesenchymal tissues.

Stem Cell Therapy Potential

Adult skin cells reprogrammed to induced pluripotent stem cells (iPSCs) via Nanog.

Sequential gene expression

Mimics developmental signaling with genes like SOX11, FOXA2, PDX1, NGN3.

Final result of stem cell therapy

β-cells capable of producing insulin, used to treat diabetes in mouse models.

Proof-of-concept

For regenerative medicine using developmental biology knowledge.

FGFs

Key regulatory factors including FGF1, FGF2, FGF10.

Retinoic acid

A key regulatory factor in development.

PDX1

A key regulatory factor in pancreas and duodenum formation.

NGN3

A key regulatory factor in endocrine progenitor development.

Sonic Hedgehog (Shh)

Suppressed in pancreatic regions.

Wnt

Context-dependent, often suppressed for pancreatic fate.

BMPs

Promote hepatic fate.

Anterior intestinal portal (AIP)

The gut begins to form as the AIP and caudal intestinal portal pinch off.

1st Pharyngeal Pouch

Contributes to tympanic cavity (middle ear) & Eustachian tube.

2nd Pharyngeal Pouch

Contributes to palatine tonsils (lymphoid aggregates).

3rd Pharyngeal Pouch

Dorsal part: Parathyroid gland; Ventral part: Thymus.

4th Pharyngeal Pouch

Contributes to parathyroid gland (further contributions) & ultimobranchial body (thyroid C-cells).

Gut tube patterning

Driven by reciprocal interactions between endoderm and splanchnic mesoderm.

Key Transcription Factors in Gut Patterning

Factors that define anterior-posterior identity via region-specific transcription.

Sox17

Specifies gut endoderm identity but lacks polarity (non-regional).

SOX2

Specifies upper digestive structures.

CDX2

Specifies midgut (small intestine).

CDXA

Specifies hindgut structures.

HHEX

Involved in liver and pancreas development.

Barx1

Mesoderm near the foregut expresses Barx1 to activate SFRPs.

SFRPs

Inhibit Wnt signaling in adjacent endoderm.

BMP4

Expression induces SOX9 and NKX2.5 for sphincter muscle formation.

Sphincter Formation

Regulates formation of sphincter muscle between stomach and small intestine.

Dorsal Mesentery

A fibrous membrane derived from mesoderm that connects the gut tube to the posterior body wall and provides positional stability and support during gut folding and rotation.

Role in Gut Folding

With mesentery: Gut forms folded, anchored loops (normal structure). Without mesentery: Gut becomes a straight, unanchored tube (abnormal development). Critical for gut tube morphogenesis and organ placement.

Gut Tube Development

The gut tube is not developing in isolation; its regionalization depends on paracrine factors from nearby mesenchyme.

Reciprocal Signaling

Ensures that the correct portions of the digestive tract form in response to gradient-based and localized transcription factor expression.

Pharynx and Gut Development

The gut tube forms through pinching in of the anterior intestinal portal (AIP) and caudal intestinal portal (CIP), resulting in three major gut regions: Foregut - anterior, Midgut - central, Hindgut - posterior.

Pharyngeal Apparatus

A segmented structure in the head and neck region, consisting of pharyngeal arches, pharyngeal pouches (endoderm-derived), and pharyngeal grooves/clefts (ectoderm-derived).

Eustachian Tube Function

Forms a connection between the middle ear and pharynx, causing 'ear-popping' when sick.

Concept of Regional Specification

Patterning of the gut is regulated through reciprocal interactions between endoderm (gut lining) and splanchnic mesoderm (surrounding tissue).

Transcription Factor Gradients in Regionalization

Key transcription factors for gut regions: Foregut → Stomach & Esophagus SOX2; Midgut → Small Intestine PDX1, CDX2; Hindgut → Colon, Rectum CDX1, CDX2, CDXA; Liver & Pancreas Buds HHEX (HHEX1).

SOX17 Function

Specifies gut endoderm identity overall (sets up gut fate), but doesn't confer positional identity.

Default Pathway = Intestine

In absence of special signaling, the gut epithelium defaults to intestinal fate due to active WNT signaling from surrounding mesoderm.