Human development days 1-4

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Human development days 1-4

HMBP Exam

HMBP Exam

Introduction to pharmacology
Light microscopy and staining methods
Cytoskeleton and intracellular motility
Pharmacodynamics: Agonist, partial agonist and antagonist
Cellular structure and function
Primary ciliary dyskinesia
Nuclear structure
DNA structure
Transcription of DNA
Translation of mRNA
Epigenetics
DNA damage and repair
DNA mutations
Rett syndrome
Amino acids and protein folding
Protein structure and synthesis
Osmosis
Myasthenia gravis
Cell membrane
Human development days 1-4
Human development days 4-7
Human development week 2
Selective permeability of the cell membrane
Prions (Spongiform encephalopathy)
Ehlers-Danlos syndrome
Osteogenesis imperfecta
Cystic fibrosis
Ectoderm
Mesoderm
Endoderm
Diabetes mellitus
Beta-thalassemia
Inheritance patterns
Independent assortment of genes and linkage
Mitosis and meiosis
Karyotyping
Glycolysis
Gluconeogenesis
Essential fructosuria
Hereditary fructose intolerance
Amino acid metabolism
Arsenic poisoning
Patau syndrome (Trisomy 13)
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Turner syndrome
Klinefelter syndrome
Angelman syndrome
Prader-Willi syndrome
Marfan syndrome
Citric acid cycle
Electron transport chain and oxidative phosphorylation
Pharmacokinetics: Drug metabolism
Pharmacokinetics: Drug elimination and clearance
Pentose phosphate pathway
Glycogen metabolism
Glycogen storage disease type I
Glycogen storage disease type II (NORD)
Glycogen storage disease type V
Glycogen storage disease type IV
Glycogen storage disease type III
Ketone body metabolism
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Cri du chat syndrome
Williams syndrome
Fatty acid synthesis
Fatty acid oxidation
Nucleotide metabolism
Cystinosis
Antimetabolites for cancer treatment
Severe combined immunodeficiency
Lesch-Nyhan syndrome
Megaloblastic anemia
Hartnup disease
Cystinuria (NORD)
Drug administration and dosing regimens
Nitrogen and urea cycle
Cell cycle
Cholesterol metabolism
Fragile X syndrome
Huntington disease
Friedreich ataxia
Polycystic kidney disease
Achondroplasia
Neurofibromatosis
Albinism
Niemann-Pick disease types A and B (NORD)
Tay-Sachs disease (NORD)
Fabry disease (NORD)
Alkaptonuria
Ornithine transcarbamylase deficiency
Homocystinuria
Maple syrup urine disease
Krabbe disease
Gaucher disease (NORD)
Niemann-Pick disease type C
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Phenylketonuria (NORD)
Folate (Vitamin B9) deficiency
Vitamin B12 deficiency
Wernicke-Korsakoff syndrome
Zellweger spectrum disorders (NORD)
Vitamin C deficiency
Adenosine deaminase deficiency
Xeroderma pigmentosum
Fanconi anemia
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Gel electrophoresis and genetic testing
Fluorescence in situ hybridization
ELISA (Enzyme-linked immunosorbent assay)
Hardy-Weinberg equilibrium
Hemochromatosis
Alpha-thalassemia
Hemophilia
Muscular dystrophy
Mitochondrial myopathy
Pharmacokinetics: Drug absorption and distribution
Pharmacodynamics: Drug-receptor interactions

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Human development begins with fertilization, which is the moment when a sperm cell and an oocyte (or egg cell) fuse to form a zygote, the seed of what will eventually grow into a human baby.

During sex, semen containing about 200 million spermatozoa (or sperm) enters the vagina.

This seminal fluid is alkaline, which means it’s capable of neutralizing acidic vaginal fluids.

The sperm quickly make their way through the cervix and uterus and swim into the fallopian tubes, which are also called the uterine tubes.

Eventually, these millions of sperm enter the ampulla of the uterine tube and then the infundibulum, an opening which flowers out next to the ovary.

By this point, most of the 200 million sperm that entered the body during sex have died for numerous reasons: some got stuck in the vaginal mucus, others ended up lost in the cervix, and the rest were killed and absorbed by the white blood cells.

About a thousand lucky survivors are left to wait in the uterine tube for the egg to arrive.

As the sperm wait, they start to rub up against the walls of the uterine tube, and that helps them remove the protective glycoprotein coat and plasma membrane covering the acrosome, a cap-like structure covering what you might think of as the sperm’s head. This process is called capacitation.

Once these protective outer layers are gone, the sperm are able to secrete an enzyme called hyaluronidase which can break down hyaluronic acid, a major component of the extracellular matrix protecting the egg.

Now, the egg is the largest cell in the human body, big and round, the size of a grain of sand.

As you’ll soon see, it’s kind of like an onion, as it’s made up of many layers.

The sperm trying to enter and fertilize this big egg are the smallest cells in the human body—about 1/30th the size of the egg—and they’re long and thin.

The most intrepid sperm make their way past the extracellular matrix surrounding the egg to a deeper layer called the corona radiata, which is made up of follicular cells.

The sperm then make their way through the corona radiata to the zona pellucida, another layer of extracellular matrix made of glycoproteins, which protects the egg. Only about 500 sperm cells make it this far!

The zona pellucida is also called the jelly coat, since it’s a clear, jelly-like covering wrapped around the egg.

The jelly coat/zona pellucida lies over another layer, this one made up of a protein called zona pellucida sperm-binding protein 3, or ZP3 protein for short.

As sperm close in on the zona pellucida, they undergo a process called the acrosome reaction, which happens in two parts.

First, the sperm release acrosin, a hydrolytic enzyme that bores a hole in the jelly-like coating of the zona pellucida.

After that, the sperm start assembling actin proteins, which fold out like a large protein crane, anchoring and binding the sperm to the ZP3 proteins.

Once the sperm is anchored to the surface of the egg, the plasma membrane overlying the sperm and the egg begin to fuse together—this is called sperm-binding.

Now, the egg contains cortical granules which are like bags of enzymes, one being peroxidase.

Key Takeaways

Human development starts with fertilization on day one. This involves the fusion of an oocyte and a spermatozoon to form a single-celled zygote. During the next 36 hours after fertilization, mitotic division or cleavage takes place, leading to two cells (known as blastomeres). Series of cleavages continue, with the second cleavage giving four blastomeres, and eight blastomeres after the third cleavage.

Around day three following fertilization, we have a mulberry-shaped 16-celled mass known as a morula. At day four to five after fertilization, the embryo now has around 100 cells. It has a single layer of large and flat cells originating from its outer cell mass, which will later give rise to the placenta. There is also another part called embryoblast made up of 10 to 30 pluripotent cells, which originate from the inner cell mass. Later on, the embryoblast becomes the fetus.