Mitogenic, chemotactic, and synthetic responses of rat periodontal ligament fibroblastic cells to polypeptide growth factors in vitro

The mitogenic, chemotactic, and synthetic responses of rat periodontal ligament (PDL) fibroblastic cells to epidermal growth factor (EGF), transforming growth factor-beta (TGF-beta), recombinant human platelet-derived growth factor (rhPDGF)-AB, rhPDGF-BB, natural (n) PDGF-AB, and insulin-like growth...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of periodontology (1970) Jg. 63; H. 6; S. 515
Hauptverfasser: Matsuda, N, Lin, W L, Kumar, N M, Cho, M I, Genco, R J
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 01.06.1992
Schlagworte:
ISSN:0022-3492
Online-Zugang:Weitere Angaben
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Abstract The mitogenic, chemotactic, and synthetic responses of rat periodontal ligament (PDL) fibroblastic cells to epidermal growth factor (EGF), transforming growth factor-beta (TGF-beta), recombinant human platelet-derived growth factor (rhPDGF)-AB, rhPDGF-BB, natural (n) PDGF-AB, and insulin-like growth factor-I (IGF-I) were examined in vitro using PDL cells obtained from the coagulum of healing tooth sockets. PDGFs and IGF-I have potent and comparable mitogenic effects on PDL fibroblastic cells. The maximum mitogenic effect of PDGFs was observed at the concentration of 10 ng/ml, whereas that of IGF-I was seen at concentrations higher than 100 ng/ml. In contrast, EGF induced moderate, and TGF-beta inhibitory mitogenic responses. The combination of rhPDGF-AB with either EGF or TGF-beta demonstrated comparable mitogenic potency, equivalent to the level of PDGF alone regardless of the mitogenic effect of other growth factors. The combination of rhPDGF-AB and IGF-I, however, showed a synergistic effect revealing the highest mitogenic effect among all individual growth factors as well as any combinations of the growth factors tested. Similarly, PDL fibroblastic cells demonstrated strong chemotactic responses to both IGF-I and PDGFs. The maximum effect was observed by IGF-I at concentrations higher than 10 ng/ml, followed by rhPDGF-BB at 0.1 ng/ml, rhPDGF-AB and nPDGF at concentrations ranging from 0.1 to 1 ng/ml. TGF-beta revealed no, and EGF slightly increased, chemotactic effects. IGF-I slightly enhanced the synthesis of total protein, whereas other factors had no significant effect. However, both rhPDGF-AB and TGF-beta stimulated collagen synthesis. On the other hand, IGF-I showed no effect on collagen synthesis, while EGF suppressed collagen synthesis. These findings suggest that rhPDGF-BB and IGF-I stimulate proliferation and chemotaxis of PDL fibroblastic cells. In addition, the combination of these growth factors further increases the mitogenic effect. rhPDGF-AB also stimulates collagen synthesis by PDL fibroblastic cells. Thus, rhPDGF-BB and IGF-I may have important roles in promotion of PDL healing, and consequently, may be useful for clinical application in periodontal regenerative procedures.
AbstractList The mitogenic, chemotactic, and synthetic responses of rat periodontal ligament (PDL) fibroblastic cells to epidermal growth factor (EGF), transforming growth factor-beta (TGF-beta), recombinant human platelet-derived growth factor (rhPDGF)-AB, rhPDGF-BB, natural (n) PDGF-AB, and insulin-like growth factor-I (IGF-I) were examined in vitro using PDL cells obtained from the coagulum of healing tooth sockets. PDGFs and IGF-I have potent and comparable mitogenic effects on PDL fibroblastic cells. The maximum mitogenic effect of PDGFs was observed at the concentration of 10 ng/ml, whereas that of IGF-I was seen at concentrations higher than 100 ng/ml. In contrast, EGF induced moderate, and TGF-beta inhibitory mitogenic responses. The combination of rhPDGF-AB with either EGF or TGF-beta demonstrated comparable mitogenic potency, equivalent to the level of PDGF alone regardless of the mitogenic effect of other growth factors. The combination of rhPDGF-AB and IGF-I, however, showed a synergistic effect revealing the highest mitogenic effect among all individual growth factors as well as any combinations of the growth factors tested. Similarly, PDL fibroblastic cells demonstrated strong chemotactic responses to both IGF-I and PDGFs. The maximum effect was observed by IGF-I at concentrations higher than 10 ng/ml, followed by rhPDGF-BB at 0.1 ng/ml, rhPDGF-AB and nPDGF at concentrations ranging from 0.1 to 1 ng/ml. TGF-beta revealed no, and EGF slightly increased, chemotactic effects. IGF-I slightly enhanced the synthesis of total protein, whereas other factors had no significant effect. However, both rhPDGF-AB and TGF-beta stimulated collagen synthesis. On the other hand, IGF-I showed no effect on collagen synthesis, while EGF suppressed collagen synthesis. These findings suggest that rhPDGF-BB and IGF-I stimulate proliferation and chemotaxis of PDL fibroblastic cells. In addition, the combination of these growth factors further increases the mitogenic effect. rhPDGF-AB also stimulates collagen synthesis by PDL fibroblastic cells. Thus, rhPDGF-BB and IGF-I may have important roles in promotion of PDL healing, and consequently, may be useful for clinical application in periodontal regenerative procedures.The mitogenic, chemotactic, and synthetic responses of rat periodontal ligament (PDL) fibroblastic cells to epidermal growth factor (EGF), transforming growth factor-beta (TGF-beta), recombinant human platelet-derived growth factor (rhPDGF)-AB, rhPDGF-BB, natural (n) PDGF-AB, and insulin-like growth factor-I (IGF-I) were examined in vitro using PDL cells obtained from the coagulum of healing tooth sockets. PDGFs and IGF-I have potent and comparable mitogenic effects on PDL fibroblastic cells. The maximum mitogenic effect of PDGFs was observed at the concentration of 10 ng/ml, whereas that of IGF-I was seen at concentrations higher than 100 ng/ml. In contrast, EGF induced moderate, and TGF-beta inhibitory mitogenic responses. The combination of rhPDGF-AB with either EGF or TGF-beta demonstrated comparable mitogenic potency, equivalent to the level of PDGF alone regardless of the mitogenic effect of other growth factors. The combination of rhPDGF-AB and IGF-I, however, showed a synergistic effect revealing the highest mitogenic effect among all individual growth factors as well as any combinations of the growth factors tested. Similarly, PDL fibroblastic cells demonstrated strong chemotactic responses to both IGF-I and PDGFs. The maximum effect was observed by IGF-I at concentrations higher than 10 ng/ml, followed by rhPDGF-BB at 0.1 ng/ml, rhPDGF-AB and nPDGF at concentrations ranging from 0.1 to 1 ng/ml. TGF-beta revealed no, and EGF slightly increased, chemotactic effects. IGF-I slightly enhanced the synthesis of total protein, whereas other factors had no significant effect. However, both rhPDGF-AB and TGF-beta stimulated collagen synthesis. On the other hand, IGF-I showed no effect on collagen synthesis, while EGF suppressed collagen synthesis. These findings suggest that rhPDGF-BB and IGF-I stimulate proliferation and chemotaxis of PDL fibroblastic cells. In addition, the combination of these growth factors further increases the mitogenic effect. rhPDGF-AB also stimulates collagen synthesis by PDL fibroblastic cells. Thus, rhPDGF-BB and IGF-I may have important roles in promotion of PDL healing, and consequently, may be useful for clinical application in periodontal regenerative procedures.
The mitogenic, chemotactic, and synthetic responses of rat periodontal ligament (PDL) fibroblastic cells to epidermal growth factor (EGF), transforming growth factor-beta (TGF-beta), recombinant human platelet-derived growth factor (rhPDGF)-AB, rhPDGF-BB, natural (n) PDGF-AB, and insulin-like growth factor-I (IGF-I) were examined in vitro using PDL cells obtained from the coagulum of healing tooth sockets. PDGFs and IGF-I have potent and comparable mitogenic effects on PDL fibroblastic cells. The maximum mitogenic effect of PDGFs was observed at the concentration of 10 ng/ml, whereas that of IGF-I was seen at concentrations higher than 100 ng/ml. In contrast, EGF induced moderate, and TGF-beta inhibitory mitogenic responses. The combination of rhPDGF-AB with either EGF or TGF-beta demonstrated comparable mitogenic potency, equivalent to the level of PDGF alone regardless of the mitogenic effect of other growth factors. The combination of rhPDGF-AB and IGF-I, however, showed a synergistic effect revealing the highest mitogenic effect among all individual growth factors as well as any combinations of the growth factors tested. Similarly, PDL fibroblastic cells demonstrated strong chemotactic responses to both IGF-I and PDGFs. The maximum effect was observed by IGF-I at concentrations higher than 10 ng/ml, followed by rhPDGF-BB at 0.1 ng/ml, rhPDGF-AB and nPDGF at concentrations ranging from 0.1 to 1 ng/ml. TGF-beta revealed no, and EGF slightly increased, chemotactic effects. IGF-I slightly enhanced the synthesis of total protein, whereas other factors had no significant effect. However, both rhPDGF-AB and TGF-beta stimulated collagen synthesis. On the other hand, IGF-I showed no effect on collagen synthesis, while EGF suppressed collagen synthesis. These findings suggest that rhPDGF-BB and IGF-I stimulate proliferation and chemotaxis of PDL fibroblastic cells. In addition, the combination of these growth factors further increases the mitogenic effect. rhPDGF-AB also stimulates collagen synthesis by PDL fibroblastic cells. Thus, rhPDGF-BB and IGF-I may have important roles in promotion of PDL healing, and consequently, may be useful for clinical application in periodontal regenerative procedures.
Author Kumar, N M
Genco, R J
Cho, M I
Matsuda, N
Lin, W L
Author_xml – sequence: 1
  givenname: N
  surname: Matsuda
  fullname: Matsuda, N
  organization: Department of Oral Biology, School of Dental Medicine, State University of New York, Buffalo
– sequence: 2
  givenname: W L
  surname: Lin
  fullname: Lin, W L
– sequence: 3
  givenname: N M
  surname: Kumar
  fullname: Kumar, N M
– sequence: 4
  givenname: M I
  surname: Cho
  fullname: Cho, M I
– sequence: 5
  givenname: R J
  surname: Genco
  fullname: Genco, R J
BackLink https://www.ncbi.nlm.nih.gov/pubmed/1625151$$D View this record in MEDLINE/PubMed
BookMark eNotkL1OwzAQgD0UlVJ4AAYkT0wk2GcnbUZU8ScVscAc2cmldZXYxnZBfQDem1R0uvtO3_3oLsjEOouEXHOW84rB_c75MakgL0Ve5gUvJmTGGEAmZAXn5CLG3YhcCjYlU17CaPAZ-X0zyW3QmuaONlscXFJNOoKyLY0Hm7Y4Ig0YvbMRI3UdDSpRj8G41tmketqbjRrQJtoZHZzuVTy2NNj3kSZHvesPHn0yLdJNcD9pS7txiQuRGku_TQrukpx1qo94dYpz8vn0-LF6ydbvz6-rh3XWCCiKTKOWHEFiy9qyA91I4ACLTugF05XsSl51xVgVDJBBK5ZKSaVFWVUFLKSoYE5u_-f64L72GFM9mHg8VFl0-1gvBCuEXIpRvDmJez1gW_tgBhUO9elv8AfrK3K6
CitedBy_id crossref_primary_10_1111_j_1708_8208_2010_00327_x
crossref_primary_10_1016_j_bbrc_2006_03_106
crossref_primary_10_1046_j_1365_2591_1999_00207_x
crossref_primary_10_1016_S0142_9612_99_00143_X
crossref_primary_10_1038_s41467_017_01955_w
crossref_primary_10_1016_S0011_8532_22_00594_8
crossref_primary_10_1111_j_1600_0765_2004_00750_x
crossref_primary_10_1902_jop_2008_070327
crossref_primary_10_1177_03635465990270051601
crossref_primary_10_1007_BF00298592
crossref_primary_10_1016_S0003_9969_01_00036_X
crossref_primary_10_2319_0003_3219_2008_078_0610_OSIOTE_2_0_CO_2
crossref_primary_10_1002_cm_20123
crossref_primary_10_1111_j_1600_051X_1996_tb00496_x
crossref_primary_10_1111_j_1600_0765_1996_tb00497_x
crossref_primary_10_1111_j_1601_5037_2009_00380_x
crossref_primary_10_1111_j_1600_0765_1998_tb02205_x
crossref_primary_10_1007_BF00298997
crossref_primary_10_1002_jcb_20605
crossref_primary_10_1006_excr_2001_5208
crossref_primary_10_1111_j_1600_0765_1999_tb02250_x
crossref_primary_10_1016_j_joms_2007_06_635
crossref_primary_10_1111_j_1600_0765_2007_01062_x
crossref_primary_10_1006_bbrc_1998_9151
crossref_primary_10_1007_BF03179936
crossref_primary_10_1016_j_cden_2009_09_001
crossref_primary_10_1089_ten_tea_2016_0163
crossref_primary_10_1902_jop_2012_120141
crossref_primary_10_1902_jop_2006_050147
crossref_primary_10_1016_j_addr_2007_03_016
crossref_primary_10_1177_00220345940730100301
crossref_primary_10_1111_etp_12020
crossref_primary_10_1111_j_1600_0765_2010_01313_x
crossref_primary_10_1007_s00784_019_03088_4
crossref_primary_10_1016_S0168_3659_01_00498_9
crossref_primary_10_1111_j_1600_051X_2007_01060_x
crossref_primary_10_1111_j_1600_051X_2005_00870_x
crossref_primary_10_1111_j_1600_9657_2011_01070_x
crossref_primary_10_1111_j_1600_0765_1996_tb00485_x
crossref_primary_10_1111_j_1600_0765_2008_01125_x
crossref_primary_10_1016_j_cden_2005_12_001
crossref_primary_10_1111_j_1600_0765_1996_tb00481_x
crossref_primary_10_1111_jre_13244
crossref_primary_10_1631_jzus_B1300062
crossref_primary_10_1111_j_1600_051X_1994_tb00733_x
crossref_primary_10_1111_j_1600_051x_2004_00521_x
crossref_primary_10_1177_0885328216686727
crossref_primary_10_1177_00220345960750090801
crossref_primary_10_1111_j_1600_051X_2005_00663_x
crossref_primary_10_1111_j_1600_0765_1997_tb01380_x
crossref_primary_10_1902_jop_2014_140083
crossref_primary_10_1111_jre_12557
crossref_primary_10_1016_j_archoralbio_2006_04_008
crossref_primary_10_3892_etm_2015_2414
crossref_primary_10_1016_S0099_2399_97_80399_8
crossref_primary_10_1111_j_1600_051X_2010_01639_x
crossref_primary_10_1034_j_1600_0765_2003_01607_x
crossref_primary_10_1111_j_1600_051X_1998_tb02363_x
crossref_primary_10_1007_BF02522484
crossref_primary_10_1177_1534734614534979
crossref_primary_10_1002_jcp_1041620308
crossref_primary_10_1002_cap_10211
crossref_primary_10_1177_00220345010800071301
crossref_primary_10_1902_jop_2007_060302
crossref_primary_10_1016_j_jconrel_2010_10_021
crossref_primary_10_1111_prd_12062
crossref_primary_10_1111_j_1600_0765_1999_tb02277_x
crossref_primary_10_1177_00220345970760090901
crossref_primary_10_1067_mod_2000_104097
crossref_primary_10_1089_ten_2006_12_ft_93
crossref_primary_10_1007_s10787_998_0021_5
crossref_primary_10_1016_j_jmbbm_2018_12_012
crossref_primary_10_1111_j_1600_0757_1993_tb00233_x
crossref_primary_10_35607_kjoa_34_1_201311_002
crossref_primary_10_1016_j_drudis_2010_05_003
crossref_primary_10_1016_j_jconrel_2011_07_004
crossref_primary_10_1002_jbm_b_30337
crossref_primary_10_3390_biom12030435
crossref_primary_10_1016_j_archoralbio_2017_09_019
crossref_primary_10_1053_j_oto_2009_10_006
crossref_primary_10_1080_08977190601060990
crossref_primary_10_1089_ten_tea_2018_0335
crossref_primary_10_1111_j_1600_0501_2011_02345_x
crossref_primary_10_4028_www_scientific_net_KEM_441_181
crossref_primary_10_3109_03008200009005642
crossref_primary_10_1002_jcb_29706
crossref_primary_10_1111_j_1600_0757_2006_00162_x
crossref_primary_10_1016_j_bbrc_2005_08_182
crossref_primary_10_4137_BTRI_S8120
crossref_primary_10_1007_s10103_007_0477_3
crossref_primary_10_1111_j_1834_7819_1997_tb06081_x
crossref_primary_10_1111_j_1601_0825_1995_tb00191_x
crossref_primary_10_1177_10454411970080030201
crossref_primary_10_1016_S0718_5391_12_70110_6
crossref_primary_10_1111_j_1472_8206_2009_00786_x
crossref_primary_10_1111_jcpe_12030
crossref_primary_10_1111_j_1600_051X_1995_tb00826_x
crossref_primary_10_3390_jpm11100944
crossref_primary_10_1016_j_cyto_2007_06_009
crossref_primary_10_1177_00220345960750030601
crossref_primary_10_1111_j_1600_0722_1997_tb00210_x
crossref_primary_10_1016_0003_9969_93_90120_B
crossref_primary_10_1111_jre_12935
crossref_primary_10_1111_prd_12522
crossref_primary_10_1016_S0168_3659_00_00232_7
crossref_primary_10_1902_jop_2007_060442
crossref_primary_10_1067_mse_2001_109559
crossref_primary_10_1002__SICI_1097_0185_199606_245_2_342__AID_AR16_3_0_CO_2_P
crossref_primary_10_1080_15321810903084673
crossref_primary_10_1007_s10266_011_0046_x
crossref_primary_10_1111_j_1600_0765_1999_tb02278_x
crossref_primary_10_1517_17425247_3_5_647
crossref_primary_10_1039_c5ib00114e
crossref_primary_10_1177_159101999800400102
crossref_primary_10_1034_j_1600_0765_2003_00640_x
crossref_primary_10_1111_jre_12921
crossref_primary_10_1002__SICI_1097_4652_199803_174_3_353__AID_JCP9_3_0_CO_2_N
crossref_primary_10_52711_0974_360X_2024_00106
crossref_primary_10_1089_pho_2011_3079
crossref_primary_10_1089_107632703768247421
crossref_primary_10_1902_jop_2007_070119
crossref_primary_10_1177_00220345990780100701
crossref_primary_10_1902_jop_2009_080502
crossref_primary_10_1128_IAI_00830_12
crossref_primary_10_1097_ID_0b013e3181dc24a9
crossref_primary_10_1016_S0003_9969_00_00099_6
crossref_primary_10_1177_00220345990780060901
crossref_primary_10_1016_0003_9969_94_90150_3
crossref_primary_10_3390_ijms23126552
crossref_primary_10_3390_ijms24098239
crossref_primary_10_1089_pho_2010_2846
crossref_primary_10_1016_j_ymthe_2004_01_016
crossref_primary_10_1111_j_1600_0765_1999_tb02245_x
crossref_primary_10_1002_jor_1100170315
crossref_primary_10_1111_j_1600_051X_1998_tb02500_x
crossref_primary_10_1007_s10439_014_1125_2
crossref_primary_10_1097_00004770_200203000_00012
crossref_primary_10_1111_j_1600_0765_1998_tb02336_x
crossref_primary_10_1902_jop_2011_110144
crossref_primary_10_1016_j_jconrel_2006_05_014
crossref_primary_10_3109_03008200109016843
crossref_primary_10_1111_j_1600_051X_1998_tb02463_x
crossref_primary_10_1016_j_cellbi_2003_12_007
crossref_primary_10_1016_S0003_9969_96_00024_6
crossref_primary_10_1111_j_1600_051X_2007_01090_x
crossref_primary_10_1016_S1532_3382_12_70025_8
crossref_primary_10_1111_j_1600_0757_2011_00432_x
crossref_primary_10_1016_j_archoralbio_2005_10_005
crossref_primary_10_1111_j_1600_0765_1997_tb00577_x
crossref_primary_10_1111_j_1601_0825_2004_00992_x
crossref_primary_10_1111_j_1600_0765_2009_01268_x
crossref_primary_10_1111_j_1524_475X_2008_00376_x
crossref_primary_10_1111_j_1600_0765_1999_tb02275_x
crossref_primary_10_1177_00220345960750041401
crossref_primary_10_1034_j_1600_9657_2001_170106_x
crossref_primary_10_1111_j_1600_0765_1998_tb02325_x
crossref_primary_10_1016_S0168_3659_97_00169_7
crossref_primary_10_1111_j_1600_0765_2008_01089_x
crossref_primary_10_1002_ar_1092400407
crossref_primary_10_1038_sj_bdj_2011_523
crossref_primary_10_1016_S8756_3282_96_00127_5
crossref_primary_10_1089_ten_2006_12_1441
crossref_primary_10_1177_00220345980770100601
crossref_primary_10_1089_ten_teb_2008_0062
crossref_primary_10_1902_jop_2008_070436
crossref_primary_10_1053_otsm_2002_31604
crossref_primary_10_1002_jor_1100130206
crossref_primary_10_1002__SICI_1097_0185_199606_245_2_361__AID_AR17_3_0_CO_2_N
crossref_primary_10_1002_JPER_19_0352
crossref_primary_10_1111_j_1600_0722_2007_00469_x
crossref_primary_10_1016_S0003_9969_99_00020_5
crossref_primary_10_1016_j_joen_2005_11_007
crossref_primary_10_1111_j_1600_051X_1997_tb00761_x
crossref_primary_10_1016_S0014_5793_98_00695_4
crossref_primary_10_1177_10454411980090030101
crossref_primary_10_1016_j_reactfunctpolym_2014_04_003
crossref_primary_10_1111_j_1600_0765_1997_tb01400_x
crossref_primary_10_1034_j_1600_0722_2002_21340_x
crossref_primary_10_1152_japplphysiol_01150_2014
crossref_primary_10_1097_BTF_0b013e3182463ca1
crossref_primary_10_1111_j_1600_0757_1997_tb00094_x
crossref_primary_10_1034_j_1601_0825_2003_02906_x
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1902/jop.1992.63.6.515
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod no_fulltext_linktorsrc
Discipline Dentistry
ExternalDocumentID 1625151
Genre Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S
Journal Article
GrantInformation_xml – fundername: NIDCR NIH HHS
  grantid: DE 08240
GroupedDBID ---
-Y1
.55
0R~
1OB
1OC
33P
34H
53G
5GY
5RE
AAEUS
AAHQN
AAIPD
AAMMB
AAMNL
AANLZ
AAQQT
AASGY
AAWTL
AAXRX
AAYCA
AAZKR
ABCUV
ABDQB
ABJNI
ABLJU
ABOCM
ABQWH
ABXGK
ACAHQ
ACCZN
ACGFO
ACGFS
ACGOF
ACMXC
ACPOU
ACXBN
ACXQS
ADBBV
ADBTR
ADEOM
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
AEFGJ
AEIGN
AENEX
AEUYR
AEYWJ
AFFNX
AFFPM
AFGKR
AFWVQ
AGHNM
AGXDD
AGYGG
AHBTC
AIACR
AIDQK
AIDYY
AITYG
AIURR
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMYDB
BFHJK
C45
CGR
CS3
CUY
CVF
CWXXS
DCZOG
DRFUL
DRMAN
DRSTM
DU5
EBS
ECM
EIF
EJD
F5P
FUBAC
GK1
HGLYW
KBYEO
L7B
LATKE
LEEKS
LUTES
LYRES
MEWTI
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
NPM
O9-
OVD
P2P
P2W
PER
RJQFR
ROL
SAMSI
SJN
SUPJJ
TEORI
UCV
UMD
USG
W99
WH7
WOHZO
WXSBR
X7M
XZL
YOJ
ZE2
ZGI
ZVN
ZZTAW
7X8
AIQQE
ID FETCH-LOGICAL-c3255-beb41e24ed0d6f2bc421227f3b70b94f619f5bc4302e02d38aa4ab36995274392
IEDL.DBID 7X8
ISSN 0022-3492
IngestDate Sat Sep 27 22:05:18 EDT 2025
Tue Aug 05 11:39:48 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 6
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3255-beb41e24ed0d6f2bc421227f3b70b94f619f5bc4302e02d38aa4ab36995274392
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 1625151
PQID 73053483
PQPubID 23479
ParticipantIDs proquest_miscellaneous_73053483
pubmed_primary_1625151
PublicationCentury 1900
PublicationDate June 1992
PublicationDateYYYYMMDD 1992-06-01
PublicationDate_xml – month: 06
  year: 1992
  text: June 1992
PublicationDecade 1990
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Journal of periodontology (1970)
PublicationTitleAlternate J Periodontol
PublicationYear 1992
SSID ssj0021430
Score 1.8323259
Snippet The mitogenic, chemotactic, and synthetic responses of rat periodontal ligament (PDL) fibroblastic cells to epidermal growth factor (EGF), transforming growth...
SourceID proquest
pubmed
SourceType Aggregation Database
Index Database
StartPage 515
SubjectTerms Animals
Cells, Cultured - cytology
Cells, Cultured - drug effects
Cells, Cultured - metabolism
Chemotaxis - drug effects
Collagen - biosynthesis
Collagen - drug effects
Female
Fibroblasts - cytology
Fibroblasts - drug effects
Fibroblasts - metabolism
Growth Substances - pharmacology
Mitosis - drug effects
Peptides - pharmacology
Periodontal Ligament - cytology
Periodontal Ligament - drug effects
Periodontal Ligament - metabolism
Rats
Rats, Inbred Strains
Title Mitogenic, chemotactic, and synthetic responses of rat periodontal ligament fibroblastic cells to polypeptide growth factors in vitro
URI https://www.ncbi.nlm.nih.gov/pubmed/1625151
https://www.proquest.com/docview/73053483
Volume 63
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LS8QwEA7rA_TiW3w7B4927ebRpiCIqIsXFw8Ke1uSNtEVadbdVfAH-L-dabvexIOXQgqBkPkymS_zYuwkFVTFLE0ir1MXSR2rSGeJjzq5p3Jc1hljqmYTaa-n-_3svsXOZ7kwFFY504mVoi5CTm_kZ4hEJaQWF6O3iHpGkW-1aaAxxxYEGjJ0LNP-jw-BoyUQ_9QKlxlvfJpZzM9ewojS9Hg7Ee2krTrqd_uyume6q_9b4RpbaexLuKwBsc5artxgS9cUE0Rt3TbZ1x2eYUTNMD8FFBhKqkqTOgVTFjD5LNEgxCGM69hZN4HgAVECVBEZKSwlT8Lr8MnQqyJ4JNvBogFOU8gHMIFpgFF4RXaLuqhw8IQ0f_oMTVsfGJbwMZyOwxZ77N48XN1GTS-GKBfIOiLrrOw4Ll0RF4nnNidPMk-9sGlsM-mRh3mFf0XMXcwLoY2RxookyxQnzsO32XwZSrfDINPea8VRc3gpOV6H2iIoEqmUtgKxs8uOZ_s7QKzT4k3pwvtkMNvhXbZdi2gwqktyDDpI49B22ftz6j5brgNu6R3lgC14POTukC3mHyiG8VGFIPz27u--AVZt0hM
linkProvider ProQuest
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Mitogenic%2C+chemotactic%2C+and+synthetic+responses+of+rat+periodontal+ligament+fibroblastic+cells+to+polypeptide+growth+factors+in+vitro&rft.jtitle=Journal+of+periodontology+%281970%29&rft.au=Matsuda%2C+N&rft.au=Lin%2C+W+L&rft.au=Kumar%2C+N+M&rft.au=Cho%2C+M+I&rft.date=1992-06-01&rft.issn=0022-3492&rft.volume=63&rft.issue=6&rft.spage=515&rft_id=info:doi/10.1902%2Fjop.1992.63.6.515&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0022-3492&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0022-3492&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0022-3492&client=summon