Target type: biologicalprocess
The process in which a relatively unspecialized cell acquires specialized features of an intermediate mesoderm cell. [GOC:dgh]
Intermediate mesoderm (IM) is a transient embryonic tissue that gives rise to various cell lineages, including nephron progenitors, endothelial cells, and smooth muscle cells. Its differentiation is a tightly regulated process orchestrated by complex signaling pathways and transcription factors.
1. **Induction and Specification:** The formation of IM is initiated by inductive signals from the surrounding tissues, particularly the paraxial mesoderm and the lateral plate mesoderm. Wnt signaling pathways, particularly Wnt4 and Wnt9b, play a crucial role in this inductive process. These signals trigger the expression of key transcription factors, such as Pax2, Lim1, and Hox genes, which specify the IM fate.
2. **Proliferation and Expansion:** Once specified, IM cells undergo rapid proliferation, expanding the IM population. This proliferation is regulated by growth factors like FGFs (fibroblast growth factors) and BMPs (bone morphogenetic proteins).
3. **Cell Fate Determination:** Within the IM, cells are further subdivided into distinct progenitors destined for specific lineages. This fate determination is governed by the interplay of transcription factors and signaling pathways.
* **Nephron progenitors:** The expression of transcription factors like Six2 and Wt1 defines nephron progenitors, which will ultimately give rise to the functional units of the kidney.
* **Endothelial cells:** Expression of transcription factors such as Etv2 and Fli1 promotes the differentiation of endothelial cells, which form the lining of blood vessels.
* **Smooth muscle cells:** Transcription factors like Myocd and Myog contribute to the formation of smooth muscle cells, which surround blood vessels and contribute to their function.
4. **Migration and Organization:** As IM cells differentiate, they migrate to their final destinations within the developing embryo. This migration is guided by chemoattractant and chemorepellent cues, ensuring proper organization of tissues.
5. **Maturation and Function:** Once in their final positions, IM-derived cells further mature and acquire their specialized functions. This process involves fine-tuning of gene expression and protein synthesis, resulting in functional nephrons, blood vessels, and smooth muscle.
The differentiation of IM cells is a dynamic process that involves intricate interactions between signaling pathways, transcription factors, and the surrounding environment. It is essential for the proper development of the kidney, vascular system, and other tissues. This intricate process is finely tuned by molecular mechanisms that ensure the correct formation of functional cell types, ultimately contributing to the overall development and health of the organism.'
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Protein | Definition | Taxonomy |
---|---|---|
Bone morphogenetic protein 4 | A bone morphogenetic protein 4 that is encoded in the genome of human. [PRO:CNA, UniProtKB:P12644] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
dorsomorphin | dorsomorphin : A pyrazolopyrimidine that is pyrazolo[1,5-a]pyrimidine which is substituted at positions 3 and 6 by pyridin-4-yl and p-[2-(piperidin-1-yl)ethoxy]phenyl groups, respectively. It is a potent, selective, reversible, and ATP-competitive inhibitor of AMPK (AMP-activated protein kinase, EC 2.7.11.31) and a selective inhibitor of bone morphogenetic protein (BMP) signaling. dorsomorphin: an AMPK inhibitor | aromatic ether; piperidines; pyrazolopyrimidine; pyridines | bone morphogenetic protein receptor antagonist; EC 2.7.11.31 {[hydroxymethylglutaryl-CoA reductase (NADPH)] kinase} inhibitor |
ldn 193189 | LDN 193189: inhibits bone morphogenetic protein signaling | pyrimidines | |
ml347 | ML347: an ALK2 inhibitor; structure in first source |