Literature DB >> 16529576

Arrest of flagellum morphogenesis with fibrous sheath immaturity of human spermatozoa.

D Escalier1.   

Abstract

Morphogenesis of the mammalian sperm flagellum is characterized by the assembly of axonemal and peri-axonemal structures. The incorporation of mitochondria into the flagellum results from complex cellular events, including flagellum compartmentalization and membrane and organelle reorganization. These events are striking in the annulus, which progressively relocates from the neck to the principal piece of the flagellum. This study presents a human sperm phenotype with failure of the annulus relocation, absence of mitochondrial sheath and a fibrous sheath at intermediate step of assembly. The sperm nucleus was fully condensed but with deep invaginations engulfing the acrosome. The distal pole of some mitochondria exhibited an unusual dense substance. This rare human sperm phenotype was found in a consanguineous patient, suggesting a genetic origin. These anomalies raise the question of the mechanisms that lead to impairment of both the annulus relocation and the deposit of proteins on the fibrous sheath during spermiogenesis.

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Year:  2006        PMID: 16529576     DOI: 10.1111/j.1439-0272.2006.00711.x

Source DB:  PubMed          Journal:  Andrologia        ISSN: 0303-4569            Impact factor:   2.775


  5 in total

1.  The expression pattern of SEPT7 correlates with sperm morphology.

Authors:  Hsin-Chih Albert Chao; Ying-Hung Lin; Yung-Che Kuo; Chiung-Jiung Shen; Hsian-Ann Pan; Pao-Lin Kuo
Journal:  J Assist Reprod Genet       Date:  2010-03-30       Impact factor: 3.412

2.  Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia.

Authors:  Marjorie Whitfield; Lucie Thomas; Emilie Bequignon; Alain Schmitt; Laurence Stouvenel; Guy Montantin; Sylvie Tissier; Philippe Duquesnoy; Bruno Copin; Sandra Chantot; Florence Dastot; Catherine Faucon; Anne Laure Barbotin; Anne Loyens; Jean-Pierre Siffroi; Jean-François Papon; Estelle Escudier; Serge Amselem; Valérie Mitchell; Aminata Touré; Marie Legendre
Journal:  Am J Hum Genet       Date:  2019-06-06       Impact factor: 11.025

3.  Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.

Authors:  Patrick Lorès; Denis Dacheux; Zine-Eddine Kherraf; Jean-Fabrice Nsota Mbango; Charles Coutton; Laurence Stouvenel; Come Ialy-Radio; Amir Amiri-Yekta; Marjorie Whitfield; Alain Schmitt; Caroline Cazin; Maëlle Givelet; Lucile Ferreux; Selima Fourati Ben Mustapha; Lazhar Halouani; Ouafi Marrakchi; Abbas Daneshipour; Elma El Khouri; Marcio Do Cruzeiro; Maryline Favier; François Guillonneau; Marhaba Chaudhry; Zeinab Sakheli; Jean-Philippe Wolf; Catherine Patrat; Gérard Gacon; Sergey N Savinov; Seyedeh Hanieh Hosseini; Derrick R Robinson; Raoudha Zouari; Ahmed Ziyyat; Christophe Arnoult; Emmanuel Dulioust; Mélanie Bonhivers; Pierre F Ray; Aminata Touré
Journal:  Am J Hum Genet       Date:  2019-11-14       Impact factor: 11.025

4.  Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.

Authors:  Mariem Ben Khelifa; Charles Coutton; Raoudha Zouari; Thomas Karaouzène; John Rendu; Marie Bidart; Sandra Yassine; Virginie Pierre; Julie Delaroche; Sylviane Hennebicq; Didier Grunwald; Denise Escalier; Karine Pernet-Gallay; Pierre-Simon Jouk; Nicolas Thierry-Mieg; Aminata Touré; Christophe Arnoult; Pierre F Ray
Journal:  Am J Hum Genet       Date:  2013-12-19       Impact factor: 11.025

5.  Assessment of the frequency of sperm annulus defects in a large cohort of patients presenting asthenozoospermia.

Authors:  Thassadite Dirami; Baptiste Rode; Jean-Philippe Wolf; Gérard Gacon; Emmanuel Dulioust; Aminata Touré
Journal:  Basic Clin Androl       Date:  2015-11-15
  5 in total

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