Metzincin metalloproteases in PGC migration and gonadal sex conversion.

ADAMTSs ADAMs Folliculogenesis Gonadal differentiation MMPs Metalloproteases Oogenesis Ovarian development PGC Sex conversion Sex determination Sex reversal Spermatogenesis Steroidogenesis Zebrafish

Journal

General and comparative endocrinology
ISSN: 1095-6840
Titre abrégé: Gen Comp Endocrinol
Pays: United States
ID NLM: 0370735

Informations de publication

Date de publication:
01 01 2023
Historique:
received: 30 04 2022
revised: 13 08 2022
accepted: 28 09 2022
pubmed: 4 10 2022
medline: 23 11 2022
entrez: 3 10 2022
Statut: ppublish

Résumé

Development of a functional gonad includes migration of primordial germ cells (PGCs), differentiations of somatic and germ cells, formation of primary follicles or spermatogenic cysts with somatic gonadal cells, development and maturation of gametes, and subsequent releasing of mature germ cells. These processes require extensive cellular and tissue remodeling, as well as broad alterations of the surrounding extracellular matrix (ECM). Metalloproteases, including MMPs (matrix metalloproteases), ADAMs (a disintegrin and metalloproteinases), and ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs), are suggested to have critical roles in the remodeling of the ECM during gonad development. However, few research articles and reviews are available on the functions and mechanisms of metalloproteases in remodeling gonadal ECM, gonadal development, or gonadal differentiation. Moreover, most studies focused on the roles of transcription and growth factors in early gonad development and primary sex determination, leaving a significant knowledge gap on how differentially expressed metalloproteases exert effects on the ECM, cell migration, development, and survival of germ cells during the development and differentiation of ovaries or testes. We will review gonad development with focus on the evidence of metalloprotease involvements, and with an emphasis on zebrafish as a model for studying gonadal sex differentiation and metalloprotease functions.

Identifiants

pubmed: 36191636
pii: S0016-6480(22)00162-9
doi: 10.1016/j.ygcen.2022.114137
pii:
doi:

Substances chimiques

Disintegrins 0
Metalloproteases EC 3.4.-

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

114137

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Jonathan J Carver (JJ)

Department of Biology, East Carolina University, Greenville, NC 27858, USA.

Yong Zhu (Y)

Department of Biology, East Carolina University, Greenville, NC 27858, USA. Electronic address: zhuy@ecu.edu.

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Classifications MeSH