The term regenerative medicine refers to a next-generational field of medical techniques in which cells are taken from patients, cultured, expanded, and returned to the patient in some manner in order to regenerate tissues or promote wound healing. The vast majority of these techniques, including cell sheet engineering – using patient-derived cell sheets to promote wound healing, and decellularized whole-organ engineering – the generation of intact organs using a decellularized scaffold along with the patient’s own cells, involve the use of stem cells with the same genotype as the original patient. Not only does this allow for the avoidance of transplant rejection, but it is also widely expected to help overcome the worldwide organ shortage.

The type of stem cell perhaps most frequently employed in these applications are known as induced pluripotent stem cells (iPSCs). iPSCS were developed by Professor Shinya Yamanaka at Kyoto University in a landmark paper in 2006.¹⁾ Professor Yamanaka was able to return fibroblasts to an undifferentiated state and confer upon them the same regenerative potential as embryonic stem cells through the induction of a combination of four transcription factors – Oct3/4, Sox2, Klf4, and c-Myc. He also demonstrated how these cells could be coerced down different lineages through the application of appropriately timed signaling factors.

In recent years, organoids have come to the forefront as a model for the application of human iPSCs in regenerative medicine. Organoids are in-vitro 3D cultured cell aggregates derivable from both iPSCs as well as somatic stem cells which are not only capable of self-organization and long term self-renewal, but which also exhibit similar morphology and function to the tissues from which they were derived.²⁾ This is achieved through the use of physical and biochemical cues, such as extracellular matrix components and niche factors, which are able to recapitulate cells' natural environment within living tissue.

Here at TCI, we have an extensive lineup of chemicals frequently used in both organoid culture and iPS generation / differentiation. Find below a table containing common medium additives used to generate tissue-specific organoids from both hSSCs and hiPSC, as well as several lists of common inhibitors and activators, organized by signaling pathway.

References

Page Top

Growth Factors

Characterized as cytokines, growth factors are the name for soluble proteins that initiate signaling cascades in cells related to proliferation, differentiation, survival, inflammation, and tissue repair.

Chemical Name	Target	Effect
rhEGF	EGFR	Ligand/Agonist
rhFGF2	FGFR	Ligand/Agonist

Products

References

• Epidermal Growth Factor Receptor Cell Proliferation Signaling Pathways
  • P. Wee, Z. Wang, Cancers 2017, 9, 52.
• Mechanisms underlying differential responses to FGF signaling
  • L. Dailey, D Ambrosetti, A. Mansukhani, C. Basilico, Cytokine Growth Factor Rev. 2005, 16, 233.

Page Top

Prostaglandin Signaling Pathway

Prostaglandins, a metabolic derivative of arachidonic acid, play key roles in vasodilation and the generation of the inflammatory response.

Chemical Name	Target	Effect
Prostaglandin E1	EP1–4	Ligand/Agonist
Prostaglandin E2	EP1–4	Ligand/Agonist

Products

References

• Pharmacology and signaling of prostaglandin receptors: Multiple roles in inflammation and immune modulation
  • A.N. Hata, R. M. Breyer, Pharmacol Ther. 2004, 103, 147.

Page Top

MAPK Signaling Pathways

The mammalian MAPK (Mitogen-Activated Protein Kinase) signaling pathways transmit a wide variety of signals from outside the cell through the activation of MAPKs, and are divided into three subgroups based on the specific MAPK at work: ERK, JNK, or p38.

ERK1/2 Signaling Pathway

The ERK/MAPK signaling pathway, playing major roles in cell proliferation and differentiation, begins via extracellular signals received at membrane-embedded receptor proteins such as receptor tyrosine kinases, integrins, and ion channels. Different combinations of ligand/receptor result in the activation of slightly different downstream effectors, but in general, signals from the receptor first reach an adaptor protein such as Shc, GRB2, or Crk, which is then transmitted via activation of a guanine nucleotide exchange factor such as SOS or C3G. This in turn allows for the activation of GTP binding proteins such as Ras and Rap1, which phosphorylate and activate the MAPKKK (MAPK Kinase Kinase) Raf, which phosphorylates and activates the MAPKK (MAPK Kinase) MEK1/2, which finally phosphorylates and activates ERK. Activated ERK dimer is then able to phosphorylate and activate downstream molecules not only in the cytoplasm but also in the nucleus.

p38 Signaling Pathway

As one of the three principal MAPK signaling pathways in mammals, the p38 MAPK signaling pathway plays a similar role as the JNK signaling pathway as a mediator of the cell’s response to environmental and genetic stress. In mammals, four isoforms exist (the p38α, p38β, p38γ, and p38δ isoforms), with p38α/β as the main isoforms. Upon direct and indirect activation via Akt, TNFα, Wip1, etc., p38α/β is able to phosphorylate and activate various targets in both the cytoplasm and nucleus, the most prominent of which being p53, MSK1/2, and HBP1. p38α/β activation also results in the downregulation of certain effector molecules such as Cdc25B and CycD1, highlighting the role that p38 plays in the cell cycle.

JNK Signaling Pathway

As one of the three principal MAPK signaling pathways in mammals, the JNK MAPK signaling pathway plays a similar role as the p38 signaling pathway as a mediator of the cell’s response to environmental and genetic stress. Upon direct and indirect activation via Akt, Tak1, TNFα, ROS, etc., JNK is able to phosphorylate and activate various targets in both the cytoplasm and nucleus, the most prominent of which being p53, PPARγ, HSP1, c-Jun, and Stat3. JNK activation also results in the downregulation of certain effector molecules such as Bcl2 and Bim, highlighting the role that JNK plays in determination of cell fate.

Chemical Name	Target	Effect
GW-5074	c-Raf	Inhibitor
Sorafenib	c-Raf, B-Raf	Inhibitor
PD 98059	MEK1/2, AHR	Inhibitor
SL 327	MEK1/2	Inhibitor
PD 184352	MEK1/2	Inhibitor
SP 600125	JNK1/2/3, Aurora A, FLT3, TRKA	Inhibitor
SU 3327	JNK	Inhibitor
SB 239063	p38α/β	Inhibitor
SB 203580	p38	Inhibitor
FR 180204	ERK1/2	Inhibitor
Honokiol	ERK1/2, Akt	ERK1/2: Activator, Akt: Inhibitor
PD 169316	p38	Inhibitor
VX-702	p38α	Inhibitor

Products

References

• A Comprehensive Review on MAPK: A Promising Therapeutic Target in Cancer
  • C. Braicu, M. Buse, C. Busuioc, R. Drula, D. Gulei, L. Raduly, A. Rusu, A. Irimie, A. G. Atanasov, O. Slaby, C. Ionescu, I. Berindan-Neagoe, Cancers 2019, 11, 1618.
• The p38 Pathway: From Biology to Cancer Therapy
  • A. Martínez-Limón, M. Joaquin, M. Caballero, F. Posas, E. de Nadal, Int. J. Mol. Sci. 2020, 21, 1913.
• The JNK Signaling Pathway in Inflammatory Skin Disorders and Cancer
  • M. B. Hammouda, A. E. Ford, Y. Liu, J. Y. Zhang, Cells 2020, 9, 857.

Page Top

PI3K/Akt Signaling Pathway

PI3K mediates conversion of PIP2 to PIP3 on the inner leaflet of the cell membrane upon recruitment to the membrane following activation of various receptor proteins including integrin, RTKs, cytokine receptors, B-cell receptors, and GPCRs. PIP3 acts as binding sites for various factors such as PDK1 and mTORC2, as well as Akt, which is activated via phosphorylation by PDK1 and mTORC2. Akt (Protein Kinase B) is a protein kinase which has as target proteins mTORC1, MDM2, Bad, CDK2, Lamin A, IKKα, FOXO1, P27, and GSK-3, among others, giving it an important role in the regulation of such cellular processes as cell growth, survival, motility, metabolism, and protein synthesis.

Chemical Name	Target	Effect
LY 294002	PI3K	Inhibitor
Miltefosine	PI3K	Inhibitor
3-Methyladenine	PI3K	Inhibitor
Quercetin	PI3K	Inhibitor
Wortmannin	PI3K	Inhibitor

Products

References

• The PI3K/AKT signaling pathway in regulatory T-cell development, stability, and function
  • S. L. Pompura, M. Dominguez-Villar, J. Leukoc. Biol. 2018, 103, 1065.
• Targeting PI3K/Akt signal transduction for cancer therapy
  • Y. He, M. M. Sun, G. G. Zhang, J. Yang, K. S. Chen, W. W. Xu, B. Li, Sig. Transduct. Target. Ther. 2021, 6, 425.

Page Top

PKC Signaling Pathway

Protein Kinase C (PKC) is a family of serine/threonine-kinases divided into three subfamilies based on which associated factors (Ca²⁺, DAG) are required for their phosphorylation-mediated activation.

Chemical Name	Target	Effect
Bisindolylmaleimide I	PKC	Inhibitor
Fasudil	PKC, etc.	Inhibitor
Staurosporine	PKC, etc.	Inhibitor

Products

References

• Protein kinase C signaling and oxidative stress
  • R. Gopalakrishna, S. Jaken, Free Radic. Biol. Med. 2000, 28, 1349.

Page Top

Wnt Signaling Pathway

The Wnt signaling pathway can be divided into the canonical and non-canonical (planar cell polarity and Wnt-calcium) pathways. In the canonical pathway, the Wnt receptor (a dimer of Fz and LRP5/6) sequesters the β-catenin destruction complex upon ligand binding, allowing the build-up of β-catenin in the nucleus. Once in the nucleus, β-catenin complexes with Tcf/Lef transcription factors to control the expression of various downstream genes. The canonical pathway plays major roles in the determination of cell fate during embryonic development, including the determination of body axis, and contributes to the regulation of differentiation and maintenance of stemness.

Chemical Name	Target	Effect
CHIR 99021	GSK-3α/β	Inhibitor
IWP-2	CK1δ	Inhibitor
IWR-1	Tankyrase	Inhibitor

Products

References

• Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
  • J. Liu, Q. Xiao, J. Xiao, C. Niu, Y. Li, X. Zhang, Z. Zhou, G. Shu, G. Yin, Sig. Transduct. Target. Ther. 2022, 7, 3.

Page Top

Cadherin Signaling Pathway

The cadherin family of genes play critical roles in calcium-dependent cell-cell contact and adhesion, in part mediating contact inhibition and epithelial-to-mesenchymal transition. The canonical cadherins are E-cadherin, N-cadherin, and P-cadherin, which associate with catenins to activate the Wnt, NFκB, Hippo, and RhoA signaling pathways.

Chemical Name	Target	Effect
DAPT	γ-Secretase	Inhibitor

Products

References

• Cadherin signaling: keeping cells in touch
  • O. Klezovitch, V. Vasioukhin, F1000Res. 2015, 4, 550.
• Cadherin Signaling in Cancer: Its Functions and Role as a Therapeutic Target
  • W. Yu, L. Yang, T. Li, Y. Zhang, Front. Oncol. 2019, , 989.
• Cleavage of E-Cadherin by Matrix Metalloproteinase-7 Promotes Cellular Proliferation in Nontransformed Cell Lines via Activation of RhoA
  • C. C. Lynch, T. Vargo-Gogola, L. M. Matrisian, B. Fingleton, J. Oncol. 2010, 530745.
• ROCK Inhibition Facilitates the Generation of Human-Induced Pluripotent Stem Cells in a Defined, Feeder-, and Serum-Free System
  • W. Lai, J. C. Ho, Y. Lee, K. Ng, K. Au, Y. Chan, C. Lau, H. Tse, C. Siu, Cell. Reprogram. 2010, 12, 641.

Page Top

Notch Signaling Pathway

The notch pathway is highly conserved among multicellular organisms due to its roles in cell-fate determination during early development as a mediator of cell/cell contact. Nascient notch receptor is transported to the cell membrane, where binding with such ligands as Jagged and DII cause it to be cleaved in turn by the ADAM family proteases and the γ-secretase complex. This results in liberation of notch’s intracellular domain (Notch-ICD), which is transported to the nucleus to act as a transcription factor upon complexing with CSL and MAML.

Products

References

• Notch signaling at a glance
  • K. Hori, A. Sen, S. Artavanis-Tsakonas, J. Cell Sci. 2013, 126, 550.
• The Notch Ligands, Jagged and Delta, Are Sequentially Processed by α-Secretase and Presenilin/γ-Secretase and Release Signaling Fragments
  • M. J. LaVoie, D. J. Selkoe, J. Biol. Chem. 2003, 278, 34427.

Page Top

Hedgehog Signaling Pathway

The Hedgehog (Hh) signaling pathway was first discovered due to the essential role it plays in body plan determination during development, but it has also been shown to be important for maintaining stem cell-ness in somatic stem cells. The mammalian Hedgehog ligands comprise three homologues (Desert – DHH, Indian – IHH, Sonic – SHH) with SHH being the most well studied. SHH binding to the Patched-1 (PTCH1) receptor abrogates PTCH1's repressive effect on Smoothened (SMO), which can then activate members of the GLI family of transcription factors, which go on to promote transcription of downstream factors.

Products

References

• Hedgehog Signaling in Development and Cancer
  • J. Jiang, C. Hui, Dev. Cell 2008, 15, 801.

Page Top

TGFβ Signaling Pathway

The receptors for the TGFβ signaling pathway are single-pass serine/threonine cell surface receptors, and are divided into two groups, type 1 and type 2 receptors. These receptors form a covalent disulfide bond with a receptor of the other type, forming a dimer which then itself dimerizes into a tetramer. The extracellular ligands this tetramer binds to, as well as the affinity and sensitivity of each subunit towards these ligands is used to separate the TGFβ family into three major groups, the TGFβ, BMP (Bone Morphogenic Protein), and Activin subgroups. Upon binding to a ligand, such proteins as Smad2/3, Smad1/5/8, and/or Tak1 are phosphorylated and activated, leading to an increase in the expression of genes related to embryonic development, cell proliferation and apoptosis. The TGFβ pathway is often dysregulated in cancer, and its inhibition is commonly required in organoid culture.

Products

References

• Bone morphogenetic protein receptor signal transduction in human disease
  • M. C. Gomez-Puerto, P. V. Iyengar, A. G. de Vinuesa, P. ten Dijke, G. Sanchez-Duffhues, J. Pathol. 2019, 247, 9.
• Opposing roles and potential antagonistic mechanism between TGF-β and BMP pathways: Implications for cancer progression
  • J. Ning, Y. Zhao, Y. Ye, J. Yu, EBioMedicine 2019, 41, 702.
• Targeting transforming growth factor-β receptors in pulmonary hypertension
  • C. Guignabert, M. Humbert, Eur. Respir. J. 2021, 57, 2002341.

Page Top

Other Organoid Culture Additives

Products

Page Top

Related Product Category Page

• Organoid Culture

Page Top