Researchers from the University of Illinois have identified a key process coordinating liver maturation and polyploidization, a state in which cells carry more than two sets of chromosomes. Their findings, published in Genees and developmentProvide insight into hepatocyte specialization that will be aid efforts in regenerative medicine.
The Human Liver Performs Over 150 Specialized Functions, Including Filtering Blood, Removing Waste, Regulating Blood Sugar, and Digesting Fats. Hepatocytes -the main cell type of the liver – are full formed by birth but remain dormant for the first few weeks of life. During this time, they gradually mature and develop specialized attributes.
For decades, biologists have wondered how liver cells mature after birth and achieve their dedicated functions. Further, how can scientists use this knowledge to improve regeneration of the liver, the only Internal Organ that can regenerate or report after injury?
“Over the past 15 to 20 years, biologists have gotten good at isolating stem cells,” said nash kalsotra, a professor of biochemistry at the university of Illinois and the Lead Author of the Paper.
“We can differentiate the stem cells into various cell types, which have lots of promise in regenerative biology. And we can provide these cells to damaged organs, but they are function poorerly beCaus Immature Fetal-Like State. Question is: ‘How do we take these rudimentary cells and help them mature?’ That’s the next frontier in bioology we need to cross, “Who is also a channel a chan zuckerburg biohub chicago investigator and a factor at the carl r. Woese Instutut for GENOMIC Center at Illinois, and the Division of Nutritional Sciences at Illinois.
Kalsotra’s lab seeks to answer this question by examining how hepatocytes normally achieve maturity after birth. For the current study, they began by evaluating the epithelial factor ESRP2, a regulatory protein know to control rna splicing in the liver. Absent in the fetus, ESRP2 is activated after birth.
“We know (ESRP2) is turned on right on the time when liver cells start to mature, but is that a coincidence, or isrp2 protein actually involved in liveristment?” Said Sushant Bangru (Ph.D., Biochemistry), the first author of the study.
Lab Members Approached this problem with a mixture of Clever Gnetics, Single-Cell Transcriptomics and Imaging Approaches, Generating Mice Models that Allowed Them to Turn ESRP2 Protein Function
ESRP2 Removal from Hepatocytes Made The Adult Livers Immature, While Earlier-That-Normal ESRP2 activation in the mouse pup livers accelerated their Maturation and Metabolic Functions. The conclusion? ESRP2 is a determinative factor with a direct effect on liver function that prompts hepatocytes’ shift to maturity.
“We have noticed that post-transcriptional regulation fin-tunes the final phases of gene expression,” Kalsotra said.
“There are many changes in alternative splicing to produce the right assortment of protein variants in a maturing liver. This is an example of a Qualitative change –using the Saming the Samme o many quantitative changes through micrornas, Which reduction the overall Amount of certain rnas and fin-tune the Amounts of Proteins in Liver Cells. “
Next, The Kalsotra Lab Worked to Find Both Direct and Indirect Targets of ESRP2, Unraveling Its Entre Regulatory Network. Surprisingly, they observed a large volume of eSRP2 binding to non-coding microrna-122 (mir-122), a knowledge regulator of hepatocyte polyploidy.
“The Liver Acquires a High Percentage of PolyPatocytes after birth, and the mechanism for hepatocyte polyploidization is through mir-1222222222222222222222222222222 Oplasm of a single cell divides into two separete Daughter Cells, ” Kalsotra said.
“The postnatal surge in Ploidy is Crucial for the Functional Specialization of Hepatocytes, and It Protects The Liver Against Future Incidentity of Cancer.”
The team found that ESRP2 activity is required for the timed production of mir-122 and liver polyploidization after birth. How ESRP2 Directs RNA splicing or optimizes the production of Mir-122 to Steer Ploidy is an outstanding question that the kalsotra lab is working to answer next.
“The liver does not have a dedicated reservoir of stem cells,” Kalsotra said.
“Once Existing, Healthy Liver Cells Can Produce New Cells in Adults. Ight Now, We’re Learning How We Can Coax The Adult cells to become immative and then back to full function
More information:
Sushant Bangru et al, ESRP2-Microrna-122 Axis Promotes The postnatal Onset of Liver Polyploidization and Maturation, Ganes & Development (2025). Doi: 10.1101/gad.352129.124
Citation: New Insights Into Liver Maturation and Specialization Cold Advance Regenative Medicine (2025, February 4) Retrieved 4 February 2025 from
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