In further investigations
of human liver cells from nearly 50 donor tissues of humans with varying degrees of body mass index (BMI) and liver fat, higher levels of CD8 + T cells were linked with higher levels of blood sugar or more advanced fatty liver disease.
Not exact matches
In November 2010 Japanese researchers announced online in Analytical Chemistry that they had built a chip that simultaneously tests how
liver, intestine and breast cancer
cells respond to cancer drugs, and in February 2010 scientists publishing in the Proceedings
of the National Academy
of Sciences USA developed a microscale replica
of the
human liver that allowed them to observe the entire life cycle
of hepatitis C, a virus that is difficult to observe in cultured
cells.
A
human liver cell contains the same DNA as a brain
cell, yet somehow it knows to code only those proteins needed for the functioning
of the
liver.
They transplanted the hepatocyte - like
cells into mice; 14 days later, some
of the corrected
cells had integrated into the rodent
liver and were able to produce
human A1AT.
Liver cells carry out hundreds
of different functions, only some
of which Lagasse has tested in mice, and it is unlikely that transplanted
cells could fulfill all
of them in
humans.
Using a mathematical model known as the Ising model, invented to describe phase transitions in statistical physics, such as how a substance changes from liquid to gas, the Johns Hopkins researchers calculated the probability distribution
of methylation along the genome in several different
human cell types, including normal and cancerous colon, lung and
liver cells, as well as brain, skin, blood and embryonic stem
cells.
If the procedure works in
humans, it would enable donated
livers from
humans, and possibly even from pigs, to be re-coated with a patient's own
cells, reducing the likelihood
of organ rejection.
In this study, the Hiroshima University researchers developed an animal model using severely immunodeficient mice whose
livers were partially populated with
human cells, in order to reconstruct elements
of the
human immune system.
Soker and his colleague Pedro Baptista built the
livers by taking ferret
livers and stripping them
of all their native
cells, leaving just the collagen «scaffold»
of the organ, which they then filled with
human liver cells.
«We are the first to engineer a whole
liver organ with
human cells,» says Shay Soker, a co-developer
of the
livers at Wake Forest University Baptist Medical Center in North Carolina.
The Zika virus taking hold
of the inner organelles
of human liver and neural stem
cells has been captured via light and electron microscopy.
Next, the research team will examine specifically whether these
liver cells obtained from
human embryonic stem
cells in a dish help repair injured
livers in preclinical animal models
of liver disease.
Neil Shay, a biochemist and molecular biologist in OSU's College
of Agricultural Sciences, was part
of a study team that exposed
human liver and fat
cells grown in the lab to extracts
of four natural chemicals found in Muscadine grapes, a dark - red variety native to the southeastern United States.
In recent years, several groups
of scientists have grown lung
cells from
human iPSCs, but the recipes aren't perfect — the resulting lung
cells grow amidst a jumble
of liver cells, intestinal
cells, and other tissues.
Stem
cells injected into lamb fetuses have created
livers that are up to 10 percent
human, says Esmail Zanjani
of the University
of Nevada at Reno.
Even more encouraging, the engineered tissues still continued to produce
human neural, cartilage, and
liver cell proteins, the team reports online this week in the Proceedings
of the National Academy
of Sciences.
Rather than artificially triggering cancer by engineering genetic mutations, this model more closely mimics
human liver cancer in that tumors develop as a natural consequence
of non-alcoholic steatohepatitis (NASH), a chronic metabolic disorder that causes
liver damage, fibrosis and numerous
cell mutations.
In a paper published in the journal Proceedings
of the National Academy
of Sciences, Sangeeta Bhatia
of MIT and Charles Rice
of Rockefeller University describe using microfabricated
cell cultures to sustain hepatitis B virus in
human liver cells, allowing them to study immune responses and drug treatments.
However, chronic
liver inflammation in both mice and
humans also led to the accumulation
of immunosuppressive lymphocytes, a type
of immune
cell Karin and Shalapour first described two years ago.
The Simon lab is now working on testing the effects
of the chimera on
human liver cells and in mouse
livers, to further elucidate its role in the disease.
For the animal experiments, Savio Woo
of the Center for Gene Therapy at Baylor College
of Medicine in Houston and his colleagues first isolated
liver cells from transgenic mice that produce the
human protein a1 - antitrypsin in their
livers, from where it is secreted into the blood.
View the video A tiny cluster
of lab - grown
human cells that sprouts into
liver tissue could one day nix the need for organ donors.
«We were excited to see that in
human liver tumors mTORC1 signaling correlates with FGF21 expression,» comments
cell biologist Dr. Marion Cornu and first author
of the study.
They tried hundreds
of different recipes; eventually they discovered that if they mixed
liver precursor
cells (derived from iPS
cells) with two other types
of standard
human cell lines known to be important for embryonic
liver development, then the
cells would spontaneously form a 4 to 5 - millimeter 3D structure called a
liver bud.
A cocktail
of human cell types mixed in a dish (inset, left) spontaneously forms a three dimensional
liver bud (inset, right) which is transplanted into a mouse for final development into a
A ONE - OFF treatment for diabetes is a step closer thanks to a better understanding
of how
human liver cells can be transformed into something like the beta
cells that produce insulin in a healthy pancreas.
Writing in the latest issue
of the journal Nature, researchers in the laboratories
of Gladstone Senior Investigator Sheng Ding, PhD, and UCSF Associate Professor Holger Willenbring, MD, PhD, reveal a new cellular reprogramming method that transforms
human skin
cells into
liver cells that are virtually indistinguishable from the
cells that make up native
liver tissue.
Geneticist Yoav Gilad
of the University
of Chicago and his colleagues used a new technique to examine the genes in the
liver cells of four primates:
humans, chimpanzees, orangutans and macaques.
Using
cells from mice and
human livers, Toronto General Hospital Research Institute researchers demonstrated for the first time how under specific conditions, such as obesity,
liver CD8 + T
cells, white blood
cells which play an important role in the control
of viral infections, become highly activated and inflammatory, reprogramming themselves into disease - driving
cells.
Now, in a new study published in the journal
Cell, scientists at the Salk Institute for Biological Studies have discovered that a synthetic form
of vitamin D, calcipotriol (a drug already approved by the FDA for the treatment
of psoriasis), deactivates the switch governing the fibrotic response in mouse
liver cells, suggesting a potential new therapy for fibrotic diseases in
humans.
Salk researchers found that a drug already approved by the FDA for the treatment
of psoriasis deactivates the switch governing the fibrotic response in mouse
liver cells, suggesting a potential new therapy for fibrotic diseases in
humans.
The new cellular and molecular data uncovered in the current study will be «exploited in the future to further improve
liver bud organoids» and «precisely recapitulate differentiation
of all
cell types» in fetal
human development, the authors write.
Additionally, overexpression
of POSTN in
human mammary epithelial and breast cancer
cells resulted in enhanced tumor growth and metastasis (Wang et al., 2013), which is similar to a colon cancer
cell model where overexpression
of POSTN resulted in an increase in the number and size
of liver metastases (Bao et al., 2004).
«Our data give us a new, detailed understanding
of the intercellular communication between developing
liver cells, and shows we can produce
human liver buds that come remarkably close to recapitulating fetal
cells from natural
human development.»
Because
of this, a major goal in regenerative medicine is to attain self - organizing
human tissues — in which
cells experience a series
of coordinated molecular events precisely timed and spaced to form functioning three dimensional
liver buds, the authors write.
However, Takebe's
liver bud has the advantage
of being grown from iPS
cells, rather than, for example, the primary
human hepatocytes used in Bhatia's graft, which could make it useful in modelling rare diseases or examining the specific genetic backgrounds
of the iPS
cell donors.
If the marriage
of stem
cells and CRISPR follows a similar path, it might not be long before pigs have enough Homo sapiens in them not only to grow
human hearts, lungs,
livers, and kidneys for transplant but also to model
human diseases more closely than current lab animals do and to test experimental drugs.
«This data allows classification
of all
human protein - coding genes into those coding for house - hold functions (present in all
cells) and those that are tissue - specific genes with highly specialized expression in particular organs and tissues, such as kidney,
liver, brain, heart, pancreas.
Until now, scientists examining the causes and effects
of insulin resistance have struggled with a general lack
of human cell lines from tissues such as muscle, fat and
liver that respond significantly to insulin, Kahn says.
Human iPS
cell - derived hepatocytes differentiated with our robust differentiation protocol and cultured using our novel maintenance medium provide an inexhaustible, consistent supply
of functional hepatocytes that can be used to advance the understanding
of diseases related to dysfunction in
liver metabolism, including NAFLD / NASH, type 2 diabetes, and metabolic syndrome.
Further research uncovered a broad spectrum
of cell surface stem
cell markers (e.g., CD133, CD44, and CD24) that allow the identification
of CSCs in
human solid tumors, including brain, breast, prostate, pancreas,
liver, ovary, skin, colon cancers, and melanoma (3 - 6)(Figure 1 based on 7).
Gladstone scientist Dr. Sheng Ding has exposed more chameleon - like qualities
of the
human skin
cell, using chemical cocktails to turn skin
cells into fully functional brain, heart,
liver, and insulin - producing pancreas
cells.
Human iPS
cell - derived hepatocytes differentiated with our robust differentiation protocol and cultured using a novel maintenance medium provide an inexhaustible, consistent supply
of functional hepatocytes that can be used to advance the understanding
of diseases related to dysfunction in
liver metabolism, including NAFLD / NASH, type 2 diabetes, and metabolic syndrome.
The cytotoxicity
of niclosamide and oxyclozanide were evaluated against HepG2
human liver carcinoma
cells and both drugs caused a dose - dependent loss in
cell viability [35,36].
«We mapped the metabolic changes caused by accumulated fat in
liver cells, and combined this data with an analysis
of biological networks
of liver and other
human tissues.
Humans obviously regenerate some
cell types very well, such as skin, muscle and
liver cells, but almost not at all in
cells of the nervous system or with any complex tissue systems.
Human umbilical cord mesenchymal stem
cells (hUCMSC) were found to improve
liver condition in rats after acute
liver failure, slowing the degeneration
of liver cells.
Researchers from the laboratories
of Hiroshi Y. Yoshikawa and Hideki Taniguchi had previously demonstrated the in vitro formation
of a 3D transplantable
liver «organ bud» from
human induced pluripotent stem
cells (iPSCs) co-cultured with mesenchymal and endothelial progenitors, and allows for the growth
of a small vascularized and functional organ [1 - 3].
Characterization
of cells in the developing
human liver.
The team perfected this system so that nearly 95 %
of the
liver cells are
of human origin, but the important question was whether they would behave like a
human livers.