Cell division, also known as mitosis, allows cells to grow, repair damaged tissue, and replace old or damaged cells. It occurs through several steps: during interphase the cell makes copies of its DNA and organelles in preparation for division; next, the condensed chromosomes align in the center of the cell during metaphase and are then pulled apart during anaphase; finally, in telophase two new daughter cells form with identical DNA and cytoplasm as the original parent cell. Precise control of the cell cycle through mitosis is essential for healthy cell growth and tissue maintenance.
Levels of organization life.
Atome-molecules-cells-tissues-organ-system-organism to the ecospehere.
With interactives exercises for the classroom lesson.
www. biodeluna.wordpress.com/
Levels of organization life.
Atome-molecules-cells-tissues-organ-system-organism to the ecospehere.
With interactives exercises for the classroom lesson.
www. biodeluna.wordpress.com/
Infer the significance of cell division.
Differentiate a DNA molecule, a chromosome, and a chromatid.
Characterize the phases of the cell cycle and their control points.
Describe the major events associated with stages of mitosis.
Explain the process of cytokinesis.
Learning Objectives
Describe the role of apoptosis in the life cycle of a cell.
Relate cancer as a result of the malfunction of the cell during the cell cycle.
A detailed presentation for the digestive system to be thought on grade 8 level (Department of Education Philippines Standards) including parts of the cell, functions, cell division, mitosis, meiosis and Mendelian genetics
This presentation talks about the cell cycle and mitosis. Also, an integration of cancer cells will be tackled in this presentation in accordance to uncontrolled cell division or mitosis.
This is the first PowerPoint in the mrexham IGCSE Biology series. It is also available on iBooks.
It covers the Cells section from life processes of the Edexcel IGCSE Biology course
Most relevant information about the cell, its discovery, types and various kinds of organelles and their function. it also focus on how molecules are transported across the cell membrane.
2018/2019
Infer the significance of cell division.
Differentiate a DNA molecule, a chromosome, and a chromatid.
Characterize the phases of the cell cycle and their control points.
Describe the major events associated with stages of mitosis.
Explain the process of cytokinesis.
Learning Objectives
Describe the role of apoptosis in the life cycle of a cell.
Relate cancer as a result of the malfunction of the cell during the cell cycle.
A detailed presentation for the digestive system to be thought on grade 8 level (Department of Education Philippines Standards) including parts of the cell, functions, cell division, mitosis, meiosis and Mendelian genetics
This presentation talks about the cell cycle and mitosis. Also, an integration of cancer cells will be tackled in this presentation in accordance to uncontrolled cell division or mitosis.
This is the first PowerPoint in the mrexham IGCSE Biology series. It is also available on iBooks.
It covers the Cells section from life processes of the Edexcel IGCSE Biology course
Most relevant information about the cell, its discovery, types and various kinds of organelles and their function. it also focus on how molecules are transported across the cell membrane.
2018/2019
A second type of cell division called meiosis takes place in multicellular eukaryotes. This is a reduction division in which the daughter cells receive exactly half the number of chromosomes of the mother cells.
Meiosis occurs in the production of gametes—the sperm of the males and the eggs of the females. When a sperm fertilizes an egg, a zygote is produced with the appropriate number of chromosomes for the species—in humans (and potatoes) the zygote and the somatic (body) cells produced from it have 46 chromosomes. This is the diploid (2n) number of chromosomes, half of which have come from the sperm nucleus, half from the egg. The sperm and egg are haploid ( n); they carry half the number of chromosomes of the body cells (in humans, 23 in each sperm and egg). Meiosis thus makes it possible to maintain a constant number of chromosomes in a species that reproduces sexually by halving the number of chromosomes in the reproductive cells. Meiosis uses many of the same mechanisms as mitosis and is assumed to have been derived from mitosis after the latter procedures were in place in some early organisms millenia ago.
Figure 1 shows the stages of mitosis, and Figure 2 shows the stages of meiosis. Note that the names for the stages are the same as those of mitosis, with the addition of a numeral to designate either the first or the second divisional stage. Both divisions are part of meiosis; not until the final four daughter cells are produced is the process complete.
Synapsis in Prophase I is a decisive interval in determining the inheritance of the daughter cells. At this time, genetic recombination can occur; that is, daughter cells may receive combined traits of their two parents rather than simply the trait from one or the other. This is possible because the phenomenon called crossing over often occurs when the chromatids lie together—segments containing similar alleles break apart and rejoin to the corresponding segment of the opposite chromatid, thus mixing the traits from individual parents.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
Richard's entangled aventures in wonderlandRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
2. Cell Division—Mitosis Notes
Cell Division — process by which
a cell divides into 2 new cells
• Why do cells need to divide?
1.Living things grow by
producing more cells, NOT
because each cell increases in
size
2.Repair of damaged tissue
3.If cell gets too big, it cannot
get enough nutrients into the
cell and wastes out of the cell
3. Skin cancer - the abnormal growth of
skin cells - most often develops on skin
exposed to the sun.
Cell reproduce constantly.
5. 5
DNA Replication
So cells need to make
a copy of the DNA
before dividing
When one of our cells
splits in two new ones
each new cell will then
it’s own copy of the
DNA
Original DNA
strand
Two new,
identical DNA
strands
6. DNA
• DNA is located in the nucleus and controls all cell activities including cell division
• When the cell does not need to divide and make more cells , DNA is found in a
Long and thread-like form called chromatin
• When the cell is getting ready to divide the DNA is found in a Doubled, coiled,
short DNA in a dividing cell is called chromosome
8. • The original cell is called the parent cell; the two new
cells it divides into are called daughter cells
• Before cell divides, the cell makes copies all of its DNA,
so each daughter cell gets a complete set of information
from parent cell
• Each daughter cell is exactly like the parent cell – same
kind and number of chromosomes as the original cell
Parent Cell
2
Daughter
Cells
9. Chromosome number
•Every organism has its own specific number of
chromosomes
Examples: Human = 46 chromosomes or 23 pairs
Dog = 78 chromosomes or 39 pairs
Goldfish = 94 chromosomes or 47 pairs
Lettuce = 18 chromosomes or 9 pairs
10. • All body cells in an organism have the same kind and
number of chromosomes
Examples: Human = 46 chromosomes
Human skin cell = 46 chromosomes
Human heart cell = 46 chromosomes
Human muscle cell = 46 chromosomes
Fruit fly = 8 chromosomes
Fruit fly skin cell = 8 chromosomes
Fruit fly heart cell = 8 chromosomes
Fruit fly muscle cell = 8 chromosomes
12. Interphase
• This is the time where the cell grows (makes all it
needs to do it’s job right)
• continues normal cell activities
• Makes a copy of it’s DNA as it is getting ready to
divide
• Makes a copy of the organelles inside
• So it makes sure it has 2 of everything and is ready
to divide
•The cell spends most of its life (90%) cycle in
Interphase
13. Mitosis – is what the division of cell is called
Each new cell will get it’s own nucleus, the same
number of chromosomes with mitosis
•Mitosis occurs in all the body cells
Why does mitosis occur?
So each new daughter cell
has nucleus with a complete
set of chromosomes
16. Chromosomes go from
spaghetti looking DNA to a
tight regular shape (coil up)
Nuclear membrane disappears
Spindle fibers form ( fibers
that will help move the
chromosomes around)
Prophase
17.
18. Chromosomes line up
in middle of cell
Spindle fibers connect
to chromosomes
Metaphase—(Middle)
22. Chromosomes uncoil back to
spaghetti like shape (they stay
like this in chromatin when not
dividing)
Nuclear membranes form
2 new nuclei are formed (one
for each cell )
Spindle fibers disappear
And the outer membrane of the
cell pinches ready to close
Telophase—(Two)
23.
24. Cytokinesis — the membrane closes off after each
new cell has the chromosomes , it’s own nucleus
,cytoplasm and organelles
•After mitosis and cytokinesis,
the cell returns to Interphase
to continue to grow and
continue it’s own cell
activities and jobs until it is
time to divide again
25. Summary: Cell Cycle
Interphase Mitosis Cytokinesis
•When cells become old or damaged, they die and
are replaced with new cells
http://www.cellsalive.com/mitosis_js.htm
26.
27.
28. Cell Division Control
•DNA controls all cell
activities including cell
division
•Some cells lose their ability
to control their rate of cell
division – the DNA of
these cells has become
damaged or changed
(mutated)
•These super-dividing cells
form masses called tumors
29. •Benign tumors are not cancer – these cells do not
spread to other parts of the body
•Malignant tumors are cancer – these cells break
loose and can invade and destroy healthy tissue
in other parts of the body
30. •Cancer is not just one
disease, but many
diseases – over 100
different types of
cancers
31. Please: Pairs of chromosomes aPPear
in Prophase
•Make: chromomes Meet in Middle
during Metaphase
•A: chromomes are pulled Apart
during Anaphase
•T: Two cells with their own nucleus
appear in Telophase
The menmonic "Please Make A Twin" makes it easier to
remember the active phases of cell division.