| Sheath cell | Lineage | Socket Cell | Lineage | Associated neurons | Remarks | Schematic rendition | |
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ADEshL
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ABarppaaaa
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ADEsoL
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H2
aa L
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Components of anterior deirid sensilla | ![]() |
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AMshL
AMshR |
ABplaapaapp
ABpraapaapp |
AMsoL
AMsoR |
ABplpaapapa
ABprpaapapa |
ADFL, ADLL, AFDL*, ASEL, ASGL, ASHL, ASIL, ASJL, ASKL, AWAL**, AWBL**, AWCL**
ADFR, ADLR, AFDR*, ASER, ASGR, ASHR, ASIR, ASJR, ASKR, AWAR**, AWBR**, AWCR** |
Components of amphid sensilla *The AFD neuron is embedded in the sheath but not associated with the amphid pore **The cilia of these neurons are enclosed by the sheath cell and not open to outside |
ref.1 |
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CEPshDL
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ABarpaaaapp
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CEPsoDL
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ABalapapppp
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CEPDL, also CEMDL in male
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Components of cephalic sensilla In males, sensory endings of CEM neurons are also found within the cephalic sensilla. CEM neurons open to the outside through a small papilla (See Ward et al, 1975 Fig. 33) |
ref.2 |
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ILshDL
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ABalaaaparr
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ILsoDL
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ABplaapaaap
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Components of inner labial sensilla |
ref.2 |
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OLLshL
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ABalpppaapd |
OLLsoL
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ABalapaaapp
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Components of outer labial lateral sensilla | See OLQ schematic below. Note however, OLL's are not associated with any CEP ending | ||
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OLQshDL
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ABarpaaaapa
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OLQsoDL
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AB arpaaaaal
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Components of outer labial dorsal and ventral quadrant sensilla |
ref.2 |
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PDEshL
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V5 papp L
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PDEsoL
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V5 papa L
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Components of posterior deirid sensilla | |||
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PHshL
PHshR |
ABplpppapaa
ABprpppapaa |
PHso1L PHso1R |
T paa L T paaR |
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Components of phasmids T cell and its daughters play a temporary role as phasmid socket cell in early larval life PHso2L is invaginated by the ciliated ending of PQR near the base of the left phasmid and provides wrapping of this neuron more posteriorly (Hall and Russell, 1991) |
ref.3 |
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| Male specific sensilla | |||||||
| HOsh | P1O ppppp | HOso | P1O ppaa | HOA, HOB, PVX |
Components of hook sensillum P10.papp, P11.ppp, P11.ppap and P12.pa are also part of the sensillum |
ref.3 |
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PCshL |
Y plppv |
PCsoL |
Y plap |
PCAL, PCBL, PCCL
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Components of postcloacal sensilla in male PChL and PChR hypodermal cells are also part of these sensilla PCCL/R have striated rootlets but lack basal bodies |
ref.3 |
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SPshDL
SPshDR |
B alpapap
B arpapap |
SPso1L
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B a(l/r)pppl
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SPDL , SPVL
SPDR, SPVR |
Components of male copulatory spicules In the adult, in each spicule, the 4 socket cells become syncytial as do the two sheath cells. SPCL/R, a pair of motor neurons, are also associated with the spicules and innervate spicule protractor muscles. Each of SPCL/R also has a sensory ending with a striated rootlet and is attached to the muscle over the base of the spicule by hemi-adherens junctions; hence they can be proprioceptive. SPCL/R do not have basal bodies. Spicule socket cells express dopamine synthesis rate-limiting enzyme CAT-2 (Lints R. and Emmons S.W. 1999). Socket cells are essential for spicule elongation and formation of spicule cuticle during male spicule morphogenesis whereas spicule neurons and sheath cells are dispensible for spicule morphogenesis (Jiang L. I. and Sternberg P. W. 1999). |
ref.3 |
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Male sensory ray structural cells (joint sheath and socket function) |
Lineage | Associated neurons | Remarks | Schematic rendition | |||
| R1st L/R | V5 (L/R) pppppapp | R1A L/R, R1B L/R | RnA has no distinct basal body but a long striated rootlet. RnB projects to the exterior and contains a basal body. RnA typically lies to one side of the channel and forms desmosomes to the structural cell more distally than does RnB. |
ref.3 |
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| R2st L/R | V6 (L/R) papapapp | R2A L/R, R2B L/R | |||||
| R3st L/R | V6 (L/R) papppapp | R3A L/R , R3B L/R | |||||
| R4st L/R | V6 (L/R) pppapapp | R4A L/R , R4B L/R | |||||
| R5st L/R | V6 (L/R) pppppapp | R5A L/R , R5B L/R | |||||
| R6st L/R | V6 (L/R) ppppaapp | R6A L/R , R6B L/R | |||||
| R7st L/R | T (L/R) apappapp | R7A L/R , R7B L/R | |||||
| R8st L/R | T (L/R) appaaapp | R8A L/R , R8B L/R | |||||
| R9st L/R | T (L/R) appapapp | R9A L/R , R9B L/R | |||||
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References: 1- Mutant sensory cilia in the nematode C. elegans. L.A. Perkins et al. Dev. Biol. (1986) 117:456-487 2- Electron microscopical reconstruction of the anterior sensory anatomy of C. elegans. S. Ward et al. J. Comp. Neurol. (1975) 160:313-338 3- C. elegans male postembryonic development of nongonadal structures. J. Sulston et al. Dev Biol. (1980) 78:542-576 4- The nerve ring of the nematode C. elegans. R. W. Ware et al. J. Comp. Neurol. 162:71-110
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