ANAT2341 Lab 5: Difference between revisions

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== 1. QUIZ ==
PRACTICAL CLASS PROGRAM:


== 2. Guest Lecturer - Sally Dunwoodie ==
• Weekly Quiz + revision (15 minutes)
{|
• Practical class activities (45 minutes)
| width=185px|[[File:Sally Dunwoodie.jpg|180px]]
Guest Lecture by Professor Sally Dunwoodie (45 minutes)
• Practical Class Revision (15 minutes)




| valign=top|'''Somitogenesis and Congenital Vertebral Malformation'''
<br><br>
Professor Sally Dunwoodie is an internationally renowned biomedical researcher at the Victor Chang Cardiac Research Institute. She has dedicated her life’s work to understanding how babies develop and to finding out why some 3-6% have birth defects. Some 4.9 million babies are born with a serious birth defect around the globe every year.


Professor Dunwoodie established and leads the Chain Reaction Program in Congenital Heart Disease, the largest Australian genome sequencing initiative in congenital heart disease. The program is discovering the genetic causes of heart defects family by family, with the promise that genetic diagnosis of birth defects will become a routine part of clinical practice.
PRACTICAL CLASS ACTIVITIES (45 minutes):


Professor Dunwoodie is also a world leader in identifying causes of vertebral defects, having discovered six of the seven genes known to cause such defects.
1. Virtual human embryo dissections and human embryo histology
2. Playdough modelling of neural, craniofacial and heart development
3. Embryo models of craniofacial development and heart development
4. Human developmental abnormalities


Professor Dunwoodie’s discoveries have already changed clinical practices and have led to genetic diagnostic tests being available worldwide. In 2017 Professor Dunwoodie’s team revealed a double breakthrough that has the potential to prevent some cases of recurrent miscarriage and multiple types of birth defects.


They discovered that deficiency in NAD, a vital molecule that is required for hundreds of activities in all cells, causes recurrent miscarriage and multiple types of birth defects in humans and mice. These defects were completely prevented with supplementation of niacin (vitamin B3) during pregnancy in mice. These discoveries from the Victor Chang Cardiac Research Institute are believed to be amongst Australia’s greatest ever in pregnancy research.


LEARNING OBJECTIVES:


[https://www.victorchang.edu.au/heart-research/embryology VCCRI - Embryology]
• Understanding development of the gastrointestinal and respiratory tracts
|}
• Understanding neural crest development
• Understanding head development
• Understanding of heart development
• Understanding of musculoskeletal development
• Understanding human birth disorders relevant to these organ systems
• Understanding research into how the environment can influence the genetic processes driving heart and musculoskeletal development


[[Media:https://moodle.telt.unsw.edu.au/pluginfile.php/3304045/mod_forum/attachment/2517784/Sally%202018.pdf|Dunwoodie Lecture Slides 2018]]


{{2018ANAT2341}}
 
 
PRACTICAL CLASS ACTIVITIES
In this practical class we will work in small groups of 4 students.
There will be 3 optional activities of which you can chose one or more. These activities will give you an improved understanding of system development in 3D.
Secondly, I would like you to investigate with your group human birth defects associated with the organ systems relevant to this practical. This will give you an improved understanding of these disorders and how they develop.
 
Optional Activity 1: Virtual human embryo dissections and histology:
In this activity you will perform digital embryo dissections and in parallel investigate the histology of human embryos that will give you improved insights into system development in 3 dimensions.
 
Please open the 3D-PDF files representing Carnegie stages 9 to 23 of the 3D Atlas of Human Development that are freely available through this link. Please download this 84Mb file at home before the practical classes. Also open the online Virtual Human Embryo resource.
 
Identify the following features in the 3D-PDF files and in the VHE histology sections, and track how they develop over time in human embryos:
 
Neural development:
• Neural plate
• Neural folds
• Neuropores
• Prosencephalon
• Mesencephalon
• Rhombencephalon
• Telencephalon
• Diencephalon
• Metencephalon
• Myelencephalon
• The cervical, cephalic, and pontine flexures
• Spinal cord
• Spinal ganglia
• Spinal nerves
• Cranial nerves
 
Gastrointestinal and respiratory tract development:
• Foregut
• Midgut (notice the herniation, and the rotations!)
• Hindgut
• Cloaca
• Allantois
• Stomach (notice the rotations)
• Liver
• Pancreas (notice how the dorsal and ventral anlagen fuse)
• Gall bladder
• Duodenum, jejunum and ileum
• Cecum, appendix, colon and rectum
• Lung buds
• Bronchial tree
• Mesenteries, intraembryonic coelom, peritoneum and pleural cavities
 
Head development:
• Branchial arch derivatives (skeletal, arteries, cranial nerve)
• Pharyngeal pouch derivatives
• Pituitary gland
• Laryngeal cartilages
• Thyroid and thymus
 
Heart development:
• Fusing primary heart tubes
• Looping of the heart tube
• Atria
• Ventricles
• Outflow tract
• Ductus venosus
• Ductus arteriosus
• Dorsal aortae: note how these fuse over time
• Pericardial cavity
 
Musculoskeletal system:
• Somites: note an increase in somites over time
• Notochord: what role does it play in somite development?
• Somite differentiation (note that cranial somites are ahead in development)
• Development of the axial skeleton
• Development of the appendicular skeleton
• Development of the skull
• Intervertebral disks
 
 
Optional Activity 2: Embryo models
Embryo models will be on display relevant to craniofacial and heart development. Please investigate them and identify the structures and processes that have been discussed in the lectures.
 
 
Optional Activity 3: Playdough modelling of neural, craniofacial and heart development
Model the various stages of heart, neural and/or craniofacial development in 3D using playdough. Make photos, annotate the structures discussed in the lectures, and upload the annotated photos in the Padlet app.
 
 
Activity 4: Human developmental abnormalities
Please select and investigate with your group one of the developmental abnormalities listed below. A number of these will be on display as specimens provided the Museum of Human Disease. Understand which systems are affected, and how these abnormalities arise during embryonic development. Write this up 250 words, and upload with your names in the forum on Moodle.
 
• Gastroschisis:
• Meckel’s diverticulum:
• Klinefelter syndrome:
• Cleft lip/palate syndrome:
• Patent foramen ovale:
• Patent ductus arteriosus:
• Achondroplasia:
• Polydactyly:
• Syndactyly:
• Scoliosis:
• Limb reduction:
• DiGeorge Syndrome:
• Treacher Collins syndrome:
• Hirschsprung’s disease:
 
 
 
GUEST LECTURE BY PROFESSOR SALLY DUNWOODIE
Professor Sally Dunwoodie is an internationally renowned biomedical researcher at the Victor Chang Cardiac Research Institute. She has dedicated her life’s work to understanding how babies develop and to finding out why some 3-6% have birth defects.
 
 
 
REVISE PRACTICAL CLASS ACTIVITIES
In the last 15 minutes we will collectively revise the activities with the entire class to wrap up this prac.

Revision as of 17:46, 17 October 2019


PRACTICAL CLASS PROGRAM:

• Weekly Quiz + revision (15 minutes) • Practical class activities (45 minutes) • Guest Lecture by Professor Sally Dunwoodie (45 minutes) • Practical Class Revision (15 minutes)


PRACTICAL CLASS ACTIVITIES (45 minutes):

1. Virtual human embryo dissections and human embryo histology 2. Playdough modelling of neural, craniofacial and heart development 3. Embryo models of craniofacial development and heart development 4. Human developmental abnormalities


LEARNING OBJECTIVES:

• Understanding development of the gastrointestinal and respiratory tracts • Understanding neural crest development • Understanding head development • Understanding of heart development • Understanding of musculoskeletal development • Understanding human birth disorders relevant to these organ systems • Understanding research into how the environment can influence the genetic processes driving heart and musculoskeletal development



  PRACTICAL CLASS ACTIVITIES In this practical class we will work in small groups of 4 students. There will be 3 optional activities of which you can chose one or more. These activities will give you an improved understanding of system development in 3D. Secondly, I would like you to investigate with your group human birth defects associated with the organ systems relevant to this practical. This will give you an improved understanding of these disorders and how they develop.

Optional Activity 1: Virtual human embryo dissections and histology: In this activity you will perform digital embryo dissections and in parallel investigate the histology of human embryos that will give you improved insights into system development in 3 dimensions.

Please open the 3D-PDF files representing Carnegie stages 9 to 23 of the 3D Atlas of Human Development that are freely available through this link. Please download this 84Mb file at home before the practical classes. Also open the online Virtual Human Embryo resource.

Identify the following features in the 3D-PDF files and in the VHE histology sections, and track how they develop over time in human embryos:

Neural development: • Neural plate • Neural folds • Neuropores • Prosencephalon • Mesencephalon • Rhombencephalon • Telencephalon • Diencephalon • Metencephalon • Myelencephalon • The cervical, cephalic, and pontine flexures • Spinal cord • Spinal ganglia • Spinal nerves • Cranial nerves

Gastrointestinal and respiratory tract development: • Foregut • Midgut (notice the herniation, and the rotations!) • Hindgut • Cloaca • Allantois • Stomach (notice the rotations) • Liver • Pancreas (notice how the dorsal and ventral anlagen fuse) • Gall bladder • Duodenum, jejunum and ileum • Cecum, appendix, colon and rectum • Lung buds • Bronchial tree • Mesenteries, intraembryonic coelom, peritoneum and pleural cavities

Head development: • Branchial arch derivatives (skeletal, arteries, cranial nerve) • Pharyngeal pouch derivatives • Pituitary gland • Laryngeal cartilages • Thyroid and thymus

Heart development: • Fusing primary heart tubes • Looping of the heart tube • Atria • Ventricles • Outflow tract • Ductus venosus • Ductus arteriosus • Dorsal aortae: note how these fuse over time • Pericardial cavity

Musculoskeletal system: • Somites: note an increase in somites over time • Notochord: what role does it play in somite development? • Somite differentiation (note that cranial somites are ahead in development) • Development of the axial skeleton • Development of the appendicular skeleton • Development of the skull • Intervertebral disks


Optional Activity 2: Embryo models Embryo models will be on display relevant to craniofacial and heart development. Please investigate them and identify the structures and processes that have been discussed in the lectures.


Optional Activity 3: Playdough modelling of neural, craniofacial and heart development Model the various stages of heart, neural and/or craniofacial development in 3D using playdough. Make photos, annotate the structures discussed in the lectures, and upload the annotated photos in the Padlet app.


  Activity 4: Human developmental abnormalities Please select and investigate with your group one of the developmental abnormalities listed below. A number of these will be on display as specimens provided the Museum of Human Disease. Understand which systems are affected, and how these abnormalities arise during embryonic development. Write this up 250 words, and upload with your names in the forum on Moodle.

• Gastroschisis: • Meckel’s diverticulum: • Klinefelter syndrome: • Cleft lip/palate syndrome: • Patent foramen ovale: • Patent ductus arteriosus: • Achondroplasia: • Polydactyly: • Syndactyly: • Scoliosis: • Limb reduction: • DiGeorge Syndrome: • Treacher Collins syndrome: • Hirschsprung’s disease:


GUEST LECTURE BY PROFESSOR SALLY DUNWOODIE Professor Sally Dunwoodie is an internationally renowned biomedical researcher at the Victor Chang Cardiac Research Institute. She has dedicated her life’s work to understanding how babies develop and to finding out why some 3-6% have birth defects.


REVISE PRACTICAL CLASS ACTIVITIES In the last 15 minutes we will collectively revise the activities with the entire class to wrap up this prac.