Pluripotent stem cells — including induced Pluripotent Stem Cells (iPSCs) and Embryonic Stem Cells (ESCs) — can theoretically become any cell type in the human body, including eggs and sperm. This represents the ultimate frontier of reproductive medicine: in-vitro gametogenesis (IVG), where gametes could be generated from skin cells. Dr. Adnan Jabbar tracks this rapidly advancing field and its implications for fertility through research at The University of Lahore.
Learn About the FutureiPSCs have already been differentiated into primordial germ cell-like cells in laboratory settings — the first step toward creating functional gametes.
Created by reprogramming adult somatic cells (e.g., skin fibroblasts) using Yamanaka factors (Oct4, Sox2, Klf4, c-Myc). This Nobel Prize-winning technology transforms ordinary cells into embryonic-like stem cells — without using actual embryos.
Derived from the inner cell mass of blastocyst-stage embryos. The original pluripotent cell line with the most extensive differentiation data. However, their use raises significant ethical considerations that limit clinical application.
The ability to create functional eggs and sperm from skin cells would revolutionize fertility medicine — eliminating age-related infertility entirely.
In 2016, Japanese researchers created functional mouse eggs entirely from iPSCs, resulting in live, fertile offspring — proof of concept.
Human iPSCs have been differentiated into primordial germ cell-like cells. The next step — functional oocytes and spermatids — remains the focus of active global research.
Experts estimate clinical IVG is 10-20 years away. Dr. Adnan Jabbar monitors this research through collaboration with The University of Lahore to ensure his patients benefit the moment breakthroughs translate to practice.
iPSCs bypass the ethical concerns of embryonic stem cells entirely — they are created from adult somatic cells, not embryos. This makes them the preferred research direction for clinical fertility applications.
As IVG technology advances, new regulatory frameworks will be needed to address the profound biological and societal implications. Dr. Adnan Jabbar advocates for responsible, guideline-driven adoption.
Not yet clinically. In mice, functional eggs have been created from iPSCs. In humans, iPSCs have been differentiated into early germ cell precursors. Full human gamete generation remains in the research phase, estimated 10-20 years from clinical application.
Pluripotent cells can become any cell type in the body (except placental). Multipotent cells (like ADSCs and MSCs) can only become a limited range of related cell types. Pluripotent = unlimited potential. Multipotent = targeted potential.
Not for direct gamete creation. However, iPSC-derived research is informing current clinical practices, and iPSC technology is used for studying reproductive disease mechanisms, drug screening, and developing new fertility treatments.
Dr. Adnan Jabbar ensures his patients benefit the moment laboratory breakthroughs translate to clinical reality.
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