Developmental Signals - TGF-beta: Difference between revisions

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Transforming Growth Factor-beta (TGF-β) this is a superfamily signaling pathway with many different roles during development.
Transforming Growth Factor-beta (TGF-β) this is a superfamily signaling pathway with many different roles during development.


[[File:TGF-beta signaling pathway.jpg|thumb|300px|TGF-beta signaling pathway<ref name="PMID21931657">21931657</ref>]]
[[File:TGF-beta signaling pathway.jpg|thumb|300px|TGF-beta signaling pathway{{#pmid:21931657|PMID21931657}}]]




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* '''A new developmental mechanism for the separation of the mammalian middle ear ossicles from the jaw'''<ref name ="PMID28179517"><pubmed>28179517</pubmed></ref> "Multiple mammalian lineages independently evolved a definitive mammalian middle ear (DMME) through breakdown of Meckel's cartilage (MC). However, the cellular and molecular drivers of this evolutionary transition remain unknown for most mammal groups. Here, we identify such drivers in the living marsupial opossum Monodelphis domestica, whose MC transformation during development anatomically mirrors the evolutionary transformation observed in fossils. Specifically, we link increases in cellular apoptosis and TGF-BR2 signalling to MC breakdown in opossums. We demonstrate that a simple change in TGF-β signalling is sufficient to inhibit MC breakdown during opossum development, indicating that changes in TGF-β signalling might be key during mammalian evolution." [[Hearing - Middle Ear Development|Middle Ear Development]]
* '''A new developmental mechanism for the separation of the mammalian middle ear ossicles from the jaw'''{{#pmid:28179517|PMID28179517}} "Multiple mammalian lineages independently evolved a definitive mammalian middle ear (DMME) through breakdown of Meckel's cartilage (MC). However, the cellular and molecular drivers of this evolutionary transition remain unknown for most mammal groups. Here, we identify such drivers in the living marsupial opossum Monodelphis domestica, whose MC transformation during development anatomically mirrors the evolutionary transformation observed in fossils. Specifically, we link increases in cellular apoptosis and TGF-BR2 signalling to MC breakdown in opossums. We demonstrate that a simple change in TGF-β signalling is sufficient to inhibit MC breakdown during opossum development, indicating that changes in TGF-β signalling might be key during mammalian evolution." [[Hearing - Middle Ear Development|Middle Ear Development]]
* '''Oocyte-derived BMP15 but not GDF9 down-regulates connexin43 expression and decreases  gap junction intercellular communication (GJIC) activity in immortalized human granulosa cells'''<ref name ="PMID24413384"><pubmed>24413384</pubmed></ref> "In the ovary, connexin-coupled gap junctions in granulosa cells play crucial roles in follicular and oocyte development as well as in corpus luteum formation. ...The suppressive effects of BMP15 on Cx43 expression were further confirmed in primary human granulosa-lutein cells obtained from infertile patients undergoing an in vitro fertilization procedure. These findings suggest that oocyte-derived BMP15 decreases GJIC activity between human granulosa cells by down-regulating Cx43 expression, most likely via a Smad-dependent signaling pathway."
 
* '''Spatio-temporal distribution of Smads and role of Smads/TGF-β/BMP-4 in the regulation of mouse bladder organogenesis'''<ref name ="PMID23620745"><pubmed>23620745</pubmed></ref> "Although Shh, TGF-β and BMP-4 regulate radial patterning of the bladder mesenchyme and smooth muscle differentiation, it is not known what transcription factors, local environmental cues or signaling cascades mediate bladder smooth muscle differentiation. ...Based on the Smad expression patterns, we suggest that individual or combinations of Smads may be necessary during mouse bladder organogenesis and may be critical mediators for bladder smooth muscle differentiation." [[Urinary Bladder Development]]
* '''Oocyte-derived BMP15 but not GDF9 down-regulates connexin43 expression and decreases  gap junction intercellular communication (GJIC) activity in immortalized human granulosa cells'''{{#pmid:24413384|PMID24413384}} "In the ovary, connexin-coupled gap junctions in granulosa cells play crucial roles in follicular and oocyte development as well as in corpus luteum formation. ...The suppressive effects of BMP15 on Cx43 expression were further confirmed in primary human granulosa-lutein cells obtained from infertile patients undergoing an in vitro fertilization procedure. These findings suggest that oocyte-derived BMP15 decreases GJIC activity between human granulosa cells by down-regulating Cx43 expression, most likely via a Smad-dependent signaling pathway."
 
* '''Spatio-temporal distribution of Smads and role of Smads/TGF-β/BMP-4 in the regulation of mouse bladder organogenesis'''{{#pmid:23620745|PMID23620745}} "Although Shh, TGF-β and BMP-4 regulate radial patterning of the bladder mesenchyme and smooth muscle differentiation, it is not known what transcription factors, local environmental cues or signaling cascades mediate bladder smooth muscle differentiation. ...Based on the Smad expression patterns, we suggest that individual or combinations of Smads may be necessary during mouse bladder organogenesis and may be critical mediators for bladder smooth muscle differentiation." [[Urinary Bladder Development]]
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==Function==
==Function==
===Implantation===
===Implantation===
Expressed at the fetal-maternal interface and implicated in the promotion of implantation and post-implantation development.<ref name ="PMID16885531"><pubmed>16885531</pubmed></ref>
Expressed at the fetal-maternal interface and implicated in the promotion of implantation and post-implantation development.{{#pmid:16885531|PMID16885531}}


==Signaling Pathway==
==Signaling Pathway==
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[[File:BMP15_evolution_among_family_members.jpg|600px]]
[[File:BMP15_evolution_among_family_members.jpg|600px]]


BMP15 evolution among family members<ref name=PMID24147118><pubmed>24147118</pubmed>| [http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0078199 PLoS One.]</ref>
BMP15 evolution among family members{{#pmid:24147118|PMID24147118}}


==Growth Differentiation Factor 9==
==Growth Differentiation Factor 9==


[[File:Bovine ovarian follicle BMP15 and GDF9 expression.jpg|thumb|300px|Bovine ovarian follicle BMP15 and GDF9 expression<ref name=PMID21401961><pubmed>21401961</pubmed>| [http://www.rbej.com/content/9/1/33 Reprod Biol Endocrinol.]</ref>]]
[[File:Bovine ovarian follicle BMP15 and GDF9 expression.jpg|thumb|300px|Bovine ovarian follicle BMP15 and GDF9 expression{{#pmid:21401961|PMID21401961}}]]
Growth Differentiation Factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) are both members of the transforming growth factor-β (TGF-β) superfamily. They have both been identified as growth factors required oocyte to granulosa cell signaling for ovarian follicle development (folliculogenesis).<ref name=PMID15454632><pubmed>15454632</pubmed></ref><ref name=PMID5531364><pubmed>5531364</pubmed></ref><ref name=PMID24313324><pubmed>24313324</pubmed></ref>
Growth Differentiation Factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) are both members of the transforming growth factor-β (TGF-β) superfamily. They have both been identified as growth factors required oocyte to granulosa cell signaling for ovarian follicle development (folliculogenesis).{{#pmid:15454632|PMID15454632}}{{#pmid:5531364|PMID5531364}}{{#pmid:24313324|PMID24313324}}


A recent study in pig has shown that  oocyte-derived BMP15 but not GDF9 is required for down-regulation of connexin43 expression leading to a decrease in intercellular gap junction communication in granulosa cells.<ref name=PMID24413384><pubmed>24413384</pubmed></ref>
A recent study in pig has shown that  oocyte-derived BMP15 but not GDF9 is required for down-regulation of connexin43 expression leading to a decrease in intercellular gap junction communication in granulosa cells.{{#pmid:24413384|PMID24413384}}




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===Articles===
===Articles===
<pubmed>19192293</pubmed>| [http://www.biomedcentral.com/1471-2148/9/28 BMC Evol Biol.]
{{#pmid:19192293}}
<pubmed>17077151</pubmed>
 
{{#pmid:17077151}}


===Online Textbooks===
===Online Textbooks===

Revision as of 22:22, 19 March 2018

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Introduction

Transforming Growth Factor-beta (TGF-β) this is a superfamily signaling pathway with many different roles during development.

TGF-beta signaling pathway[1]


TGF Members: AMH

Factor Links: AMH | hCG | BMP | sonic hedgehog | bHLH | HOX | FGF | FOX | Hippo | LIM | Nanog | NGF | Nodal | Notch | PAX | retinoic acid | SIX | Slit2/Robo1 | SOX | TBX | TGF-beta | VEGF | WNT | Category:Molecular

Some Recent Findings

  • A new developmental mechanism for the separation of the mammalian middle ear ossicles from the jaw[2] "Multiple mammalian lineages independently evolved a definitive mammalian middle ear (DMME) through breakdown of Meckel's cartilage (MC). However, the cellular and molecular drivers of this evolutionary transition remain unknown for most mammal groups. Here, we identify such drivers in the living marsupial opossum Monodelphis domestica, whose MC transformation during development anatomically mirrors the evolutionary transformation observed in fossils. Specifically, we link increases in cellular apoptosis and TGF-BR2 signalling to MC breakdown in opossums. We demonstrate that a simple change in TGF-β signalling is sufficient to inhibit MC breakdown during opossum development, indicating that changes in TGF-β signalling might be key during mammalian evolution." Middle Ear Development
  • Oocyte-derived BMP15 but not GDF9 down-regulates connexin43 expression and decreases gap junction intercellular communication (GJIC) activity in immortalized human granulosa cells[3] "In the ovary, connexin-coupled gap junctions in granulosa cells play crucial roles in follicular and oocyte development as well as in corpus luteum formation. ...The suppressive effects of BMP15 on Cx43 expression were further confirmed in primary human granulosa-lutein cells obtained from infertile patients undergoing an in vitro fertilization procedure. These findings suggest that oocyte-derived BMP15 decreases GJIC activity between human granulosa cells by down-regulating Cx43 expression, most likely via a Smad-dependent signaling pathway."
  • Spatio-temporal distribution of Smads and role of Smads/TGF-β/BMP-4 in the regulation of mouse bladder organogenesis[4] "Although Shh, TGF-β and BMP-4 regulate radial patterning of the bladder mesenchyme and smooth muscle differentiation, it is not known what transcription factors, local environmental cues or signaling cascades mediate bladder smooth muscle differentiation. ...Based on the Smad expression patterns, we suggest that individual or combinations of Smads may be necessary during mouse bladder organogenesis and may be critical mediators for bladder smooth muscle differentiation." Urinary Bladder Development
More recent papers
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Search term: TGF-β Embryology

<pubmed limit=5>TGF-β Embryology</pubmed>

Structure

The TGF precursor protein has three distinct regions:

  1. signal peptide - targets it to the endoplasmic reticulum and secretion
  2. propeptide - or the latency associated peptide
  3. mature peptide - cleaved from the precursor protein and is actively involved in signalling
  • cleaved by Furin - a convertase
  • cleaved at a dibasic arginine-X-X-arginine (RXXR) site

Function

Implantation

Expressed at the fetal-maternal interface and implicated in the promotion of implantation and post-implantation development.[5]

Signaling Pathway

TGF-beta signaling pathway[6]

Receptor

  1. active peptide forms a hetero- or homodimer
  2. binds to a specific TGF-β Type II receptor
  3. Type II receptor then recruits a TGF-β Type I receptor
  4. phosphorylates it via its serine/threonine kinase domain
  5. phosphorylated Type I receptors then phosphorylate receptor-associated Smad proteins (R-Smads), including Smad1/5 and Smad2/3
  • Type II receptor - MlTgfRII
  • Type I receptors - MlTgfRIa, MlTgfRIb, and MlTgfRIc

Intracellular Signaling

  • R-Smad proteins are composed of two main functional domains
    • Mad-homology domains 1 and 2 (MH1 and MH2)
  • Smad1/5 - associated with BMP-like signalling.
  • Smad2/3 - associated with TGF-β-like signaling.

SMAD

SMAD5

Mothers against decapentaplegic homolog 5 (SMAD5) is a transcriptional modulator activated by BMP (bone morphogenetic proteins) type 1 receptor kinase.

OMIM: SMAD5

Bone morphogenetic protein 15

BMP15 evolution among family members.jpg

BMP15 evolution among family members[7]

Growth Differentiation Factor 9

Bovine ovarian follicle BMP15 and GDF9 expression[8]

Growth Differentiation Factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) are both members of the transforming growth factor-β (TGF-β) superfamily. They have both been identified as growth factors required oocyte to granulosa cell signaling for ovarian follicle development (folliculogenesis).[9][10][11]

A recent study in pig has shown that oocyte-derived BMP15 but not GDF9 is required for down-regulation of connexin43 expression leading to a decrease in intercellular gap junction communication in granulosa cells.[3]


Links: TGF-beta | Bone Morphogenetic Protein | Oocyte Development | Ovary Development | Menstrual Cycle | OMIM - GDF9

OMIM

About OMIM "Online Mendelian Inheritance in Man OMIM is a comprehensive, authoritative, and timely compendium of human genes and genetic phenotypes. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 12,000 genes. OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries contain copious links to other genetics resources." OMIM


References

  1. Pang K, Ryan JF, Baxevanis AD & Martindale MQ. (2011). Evolution of the TGF-β signaling pathway and its potential role in the ctenophore, Mnemiopsis leidyi. PLoS ONE , 6, e24152. PMID: 21931657 DOI.
  2. Urban DJ, Anthwal N, Luo ZX, Maier JA, Sadier A, Tucker AS & Sears KE. (2017). A new developmental mechanism for the separation of the mammalian middle ear ossicles from the jaw. Proc. Biol. Sci. , 284, . PMID: 28179517 DOI.
  3. 3.0 3.1 Chang HM, Cheng JC, Taylor E & Leung PC. (2014). Oocyte-derived BMP15 but not GDF9 down-regulates connexin43 expression and decreases gap junction intercellular communication activity in immortalized human granulosa cells. Mol. Hum. Reprod. , 20, 373-83. PMID: 24413384 DOI.
  4. Islam SS, Mokhtari RB, Kumar S, Maalouf J, Arab S, Yeger H & Farhat WA. (2013). Spatio-temporal distribution of Smads and role of Smads/TGF-β/BMP-4 in the regulation of mouse bladder organogenesis. PLoS ONE , 8, e61340. PMID: 23620745 DOI.
  5. Jones RL, Stoikos C, Findlay JK & Salamonsen LA. (2006). TGF-beta superfamily expression and actions in the endometrium and placenta. Reproduction , 132, 217-32. PMID: 16885531 DOI.
  6. Pang K, Ryan JF, Baxevanis AD, Martindale MQ (2011) Evolution of the TGF-β Signaling Pathway and Its Potential Role in the Ctenophore, Mnemiopsis leidyi. PLoS ONE 6(9): e24152 PLoS ONE
  7. Auclair S, Rossetti R, Meslin C, Monestier O, Di Pasquale E, Pascal G, Persani L & Fabre S. (2013). Positive selection in bone morphogenetic protein 15 targets a natural mutation associated with primary ovarian insufficiency in human. PLoS ONE , 8, e78199. PMID: 24147118 DOI.
  8. Hosoe M, Kaneyama K, Ushizawa K, Hayashi KG & Takahashi T. (2011). Quantitative analysis of bone morphogenetic protein 15 (BMP15) and growth differentiation factor 9 (GDF9) gene expression in calf and adult bovine ovaries. Reprod. Biol. Endocrinol. , 9, 33. PMID: 21401961 DOI.
  9. McNatty KP, Moore LG, Hudson NL, Quirke LD, Lawrence SB, Reader K, Hanrahan JP, Smith P, Groome NP, Laitinen M, Ritvos O & Juengel JL. (2004). The oocyte and its role in regulating ovulation rate: a new paradigm in reproductive biology. Reproduction , 128, 379-86. PMID: 15454632 DOI.
  10. Lodemann E & Wacker A. (1970). [Interferon-induction by Poly (A)-2 Poly (I)]. Naturwissenschaften , 57, 673. PMID: 5531364
  11. Lin ZL, Li YH, Xu YN, Wang QL, Namgoong S, Cui XS & Kim NH. (2014). Effects of growth differentiation factor 9 and bone morphogenetic protein 15 on the in vitro maturation of porcine oocytes. Reprod. Domest. Anim. , 49, 219-27. PMID: 24313324 DOI.

Reviews

Articles

Huminiecki L, Goldovsky L, Freilich S, Moustakas A, Ouzounis C & Heldin CH. (2009). Emergence, development and diversification of the TGF-beta signalling pathway within the animal kingdom. BMC Evol. Biol. , 9, 28. PMID: 19192293 DOI.

Gadue P, Huber TL, Paddison PJ & Keller GM. (2006). Wnt and TGF-beta signaling are required for the induction of an in vitro model of primitive streak formation using embryonic stem cells. Proc. Natl. Acad. Sci. U.S.A. , 103, 16806-11. PMID: 17077151 DOI.

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Cite this page: Hill, M.A. (2024, March 28) Embryology Developmental Signals - TGF-beta. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Developmental_Signals_-_TGF-beta

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