Bio 127 - Section I Introduction to Developmental Biology

1. Bio 127 - Section IIntroduction to Developmental Biology Cell-Cell Communication in Development Gilbert 9e – Chapter 3

2. It has to be EXTREMELY well coordinated for the single-celled fertilized ovum to develop into the complex adult • This coordination requires a systematic way for the cells to know what’s happening around them so that they can change their gene expression correctly • They must also then change the signals they are sending out to let surrounding cells know what changes they are making

3. Developmental Activities Coordinated in this Way 1. The formation of tissues from a mix of individual cells 2. The formation of organs from a mix of tissue types 3. The formation of cells, tissues and organs in specific locations 4. The growth and death of cells, tissues and organs 5. The achievement of polarity in cells, tissue and organs

4. The plasma membranes of cells are designed to sense what is happening in their environment • Membrane molecules sense: • other cell membranes • soluble signals sent by other cells • the type of extracellular matrix that surrounds them • A few signals can get past the plasma membrane

5. Most cells in the embryo have molecules on their surface that identify who they are These molecules also instruct them who they should be in contact with

6. Sorting out and reconstruction of spatial relationships in aggregates of embryonic amphibian cells All cell types can do it

7. Aggregates formed by mixing 7-day chick embryo neural retina cells with pigmented retina cells ....just to show that it’s more than an artist’s rendition....

8. Figure 3.4 Hierarchy of cell sorting in order of decreasing surface tensions The more adhesive the cell’s plasma membrane is, the more it migrates to the middle of a cell mixture.

9. The molecular biology of cell adhesion: Cadherins The calcium-dependent adhesion molecules (or cadherins) are the main source of adhesive activity on the cell surface The more you express, the more central you become in a mixture

10. Importance of amount of cadherin for morphogenesis --- A nearly perfect linear relationship

11. Importance of type of cadherin for morphogenesis Early embryo cells all express E-cadherin Presumptive neural tube cells lose E-cadherin and gain N-cadherin. N-cadherin expression does something very similar in limb cartilage.

12. Cadherins can activate migration through actin Cadherin binding outside of the cell can cause actin-based migration in some cells

13. Disruption of N-Cadherin in Frog Embryos failed migration failed actin assembly blocked normal

14. The cadherins activate migration through Rho GTPase Migratory cells have Rho in their cadherin-actin apparatus – cadherin activates Rho, Rho activates actin-myosin migration.

15. Drosophilagastrulation The cells that have Rho activated migrate to become the mesoderm.

16. Migration is started by expression of Twist and Snailwhich causes Rho and B-catenin to translocate in cells Rho build-up on E-cad causes actin polymerization and migration

17. Tracheal Development in Drosophila Rho can also be linked to cell surface receptors and cause chemotactic migration. The cadherin attachments remain strong and the cells migrate as a cohesive unit.

18. Figure 3.12 Cell migration Mesenchymal Cell Migration is also Rho-Dependent - not always cadherin-dependent however!

19. One-Way, Two-Way and Reciprocal Communications Strategies Ligands Receptors 2nd Messengers Target Mechanisms

20. Cell Signaling Terminology • Paracrine • Endocrine • Synaptic • Induction • Inducer • Responder • Signal Competence • Signal Transduction • Permissive Signals • Instructive Signals

21. Ectodermal competence and the ability to respond to the optic vesicle inducer in Xenopus

22. HOW? • Optic vesicle secretes...... • BMP 4 • Fgf 8 • Head ectoderm expresses...... • Sox 2 • L-Maf • Pax 6 • Lens genes turned on...... • crystallin • others

23. Induced Differentiation

24. Induction Cascades • We know that tissues tend to aggregate through cell contact • It’s common for tissues to play off each other to produce an organ • Anything from two tissues signaling back and forth to many tissues coordinating each other’s actions • The common theme is that a change in gene expression internally (TF’s, functional proteins) is often accompanied by a change in secreted proteins (paracrine, endocrine factors)

25. Eye formation is a classically studied cascade of induction Simple lens induction...

26. Reciprocal induction

29. The reciprocal interaction between an epithelium and a closely associated mesenchyme is a very common means of organ development (organogenesis)

30. These are backwards

31. Different mesenchyme induces different epithelial structures

32. Also, different epithelium can only become what they are competent to become

33. A little about some of the actual molecules..... • Growth Factors carry most of the signals • Hormones and neurotransmitters later on • 4 big families: • FGF, Hedgehog, Wnt, TGF-b • Receptors and signaling cascades premade for them make you competent

34. Fibroblast growth factor (FGF) family are classic growth factors: FGF 1-8 • lots of others: VEGF, HGF, PDGF, etc. • can change transcription of genes 2 ways • RTK Pathway: receptor tyrosine kinase • JAK-STAT: JAK activates STAT TF’s

35. Optic vesicle secretes...... • BMP 4 • Fgf 8 • Head ectoderm expresses...... • Sox 2 • L-Maf • Pax 6 • Lens genes turned on...... • crystallin • others

36. Figure 3.20 Fgf8 in the developing chick (Part 1)

37. Figure 3.20 Fgf8 in the developing chick (Part 2) FGF8 in optic vesicle L-Maf expression in ectoderm

38. Figure 3.24 A mutation in the gene for FgfR3 causes the premature constitutive activation of the STAT pathway and the production of phosphorylated Stat1 protein

39. Hedgehog family includes sonic (shh), desert (dhh) andindian (ihh) in vertebrates • Change transcription through an interesting series of inhibitory activities • the patched receptor inhibits the smoothened protein until hedgehog binds • smoothened then moves to inhibit proteins that inhibit the Gli activator protein

40. Figure 3.26 (A) Sonic hedgehog expression is shown by in situ hybridization in the nervous system, gut, and limb bud of a chick embryo. (B) Head of a cyclopic lamb Both shh and patched proteins require cholesterol. Blocking its production can cause cyclopism.

41. Wnt family has 15 members in vertebrates • Glycoproteins with lipid tails! • Work through frizzled receptors and disheveled activators (fly guys!) • Also activate by inhibition of an inhibitor

42. Interestingly, Wnt can do much of what cadherins can do • Send catenins to the nucleus • Activate rho and change the cytoskeleton • This is called “crosstalk” and it is very important in cell signaling

43. Remember the structure of the cadherin system • Implantation of the mammalian embryo in adhere to the uterine wall • E- and P-cadherin • Integrin and uterine ECM • Proteins that bind sugars on uterine wall Rho proteins associate with catenins and actin system. They can change actin’s structure.

44. The TGF-bsuperfamily is a very large family of very active peptide growth factors • involved in the development of most tissues • The receptors are also a large family of proteins • They are serine-threoninekinases, not RTK • They work through the activation of SMAD transcription factors

45. Figure 3.29 Relationships among members of the TGF-β superfamily We’ll hear a lot of these names again this semester!

46. Remember: • The Big 4 are just part of the story • We’ll talk about others as they come into play

47. The Delta-Notch family: “Juxtacrine” signals • Transmembrane proteins on cells in contact • Delta, Jagged or Serrate bind to Notch family • Signals go both ways • The Notch signal is interesting in that it’s internal domain is cleaved and enters nucleus • This activates a dormant transcription factor

48. Figure 3.33 Mechanism of Notch activity

49. Apoptosis: genetically programmed cell death • Absolutely essential to control cell numbers, cell quality and to create space • The space between our fingers • 2/3 of all neurons we make • The middle ear • The cerebral ventricles • Frog tails • Male mammary epithelium

50. Figure 3.32 Disruption of normal brain development by blocking apoptosis